| geneid | 1379 |
|---|---|
| ensemblid | ENSG00000197721.17 |
| hgncid | 2335 |
| symbol | CR1L |
| name | complement C3b/C4b receptor 1 like |
| refseq_nuc | NM_175710.2 |
| refseq_prot | NP_783641.1 |
| ensembl_nuc | ENST00000508064.7 |
| ensembl_prot | ENSP00000421736.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 207645133 |
| end | 207723703 |
| strand | + |
| ver | v1.2 |
| region | chr1:207645133-207723703 |
| region5000 | chr1:207640133-207728703 |
| regionname0 | CR1L_chr1_207645133_207723703 |
| regionname5000 | CR1L_chr1_207640133_207728703 |
| 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 | 0/0 | 569 | 74 | 19 | 7 | 34 | 3 | 11 | 28 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0002 | 0/0 | 569 | 65 | 19 | 11 | 30 | 1 | 4 | 19 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0003 | 0/0 | 569 | 56 | 1 | 27 | 15 | 7 | 6 | 14 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0004 | 0/0 | 569 | 49 | 1 | 6 | 37 | 1 | 4 | 29 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0005 | 0/1 | 569 | 23 | 4 | 7 | 6 | 3 | 2 | 4 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0006 | 0/0 | 569 | 17 | 2 | 6 | 8 | 1 | 0 | 6 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0007 | 1/0 | 569 | 14 | 13 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0008 | 0/0 | 569 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0009 | 0/0 | 569 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0010 | 0/0 | 569 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0011 | 0/0 | 569 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0012 | 0/0 | 569 | 3 | 0 | 0 | 1 | 0 | 2 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0013 | 0/0 | 569 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0014 | 0/0 | 569 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0015 | 0/0 | 569 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0016 | 0/0 | 569 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0017 | 0/0 | 569 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0018 | 0/0 | 569 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0019 | 0/0 | 569 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0020 | 0/0 | 569 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0021 | 0/0 | 569 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0022 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0023 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0024 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0025 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0026 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0027 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0028 | 0/0 | 569 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0029 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0030 | 0/0 | 569 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0031 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0032 | 0/0 | 569 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| 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 | 0/0 | 1710 | 69 | 17 | 7 | 31 | 3 | 11 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0002 | 0/0 | 1710 | 64 | 19 | 11 | 29 | 1 | 4 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0003 | 0/0 | 1710 | 51 | 1 | 26 | 11 | 7 | 6 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0004 | 0/0 | 1710 | 49 | 1 | 6 | 37 | 1 | 4 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0005 | 0/1 | 1710 | 22 | 4 | 7 | 5 | 3 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0006 | 0/0 | 1710 | 17 | 2 | 6 | 8 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0007 | 1/0 | 1710 | 14 | 13 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0008 | 0/0 | 1710 | 5 | 0 | 1 | 4 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0009 | 0/0 | 1710 | 4 | 2 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0010 | 0/0 | 1710 | 4 | 3 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0011 | 0/0 | 1710 | 3 | 0 | 0 | 3 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0012 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0013 | 0/0 | 1710 | 3 | 0 | 0 | 3 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0014 | 0/0 | 1710 | 3 | 0 | 0 | 1 | 0 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0015 | 0/0 | 1710 | 3 | 0 | 2 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0016 | 0/0 | 1710 | 2 | 1 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0017 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0018 | 0/0 | 1710 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0019 | 0/0 | 1710 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0020 | 0/0 | 1710 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0021 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0022 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0023 | 0/0 | 1710 | 2 | 0 | 1 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0024 | 0/0 | 1710 | 2 | 0 | 0 | 0 | 0 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0025 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0026 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0027 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0028 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0029 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0030 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0031 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0032 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0033 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0034 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0035 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0036 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0037 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| c0038 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| 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 | 120 | 346 | 80 | 74 | 140 | 16 | 34 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0030 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| 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 | 0/0 | 1710 | 69 | 17 | 7 | 31 | 3 | 11 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0001c0013 | 0/0 | 1710 | 3 | 0 | 0 | 3 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0001c0017 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0002c0002 | 0/0 | 1710 | 64 | 19 | 11 | 29 | 1 | 4 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0002c0035 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0003c0003 | 0/0 | 1710 | 51 | 1 | 26 | 11 | 7 | 6 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0003c0008 | 0/0 | 1710 | 5 | 0 | 1 | 4 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0004c0004 | 0/0 | 1710 | 49 | 1 | 6 | 37 | 1 | 4 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0005c0005 | 0/1 | 1710 | 22 | 4 | 7 | 5 | 3 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0005c0036 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0006c0006 | 0/0 | 1710 | 17 | 2 | 6 | 8 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0007c0007 | 1/0 | 1710 | 14 | 13 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0008c0012 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0008c0027 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0009c0010 | 0/0 | 1710 | 4 | 3 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0010c0009 | 0/0 | 1710 | 4 | 2 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0011c0015 | 0/0 | 1710 | 3 | 0 | 2 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0012c0014 | 0/0 | 1710 | 3 | 0 | 0 | 1 | 0 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0013c0011 | 0/0 | 1710 | 3 | 0 | 0 | 3 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0014c0023 | 0/0 | 1710 | 2 | 0 | 1 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0015c0024 | 0/0 | 1710 | 2 | 0 | 0 | 0 | 0 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0016c0016 | 0/0 | 1710 | 2 | 1 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0017c0020 | 0/0 | 1710 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0018c0021 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0019c0022 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0020c0019 | 0/0 | 1710 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0021c0018 | 0/0 | 1710 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0022c0032 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0023c0033 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0024c0029 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0025c0030 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0026c0031 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0027c0034 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0028c0028 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0029c0026 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0030c0037 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0031c0025 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0032c0038 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1829 | 69 | 17 | 7 | 31 | 3 | 11 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0001c0013t0001 | 0/0 | 1829 | 3 | 0 | 0 | 3 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0001c0017t0001 | 0/0 | 1829 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0002c0002t0001 | 0/0 | 1829 | 64 | 19 | 11 | 29 | 1 | 4 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0002c0035t0001 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0003c0003t0001 | 0/0 | 1829 | 51 | 1 | 26 | 11 | 7 | 6 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0003c0008t0001 | 0/0 | 1829 | 5 | 0 | 1 | 4 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0004c0004t0001 | 0/0 | 1829 | 49 | 1 | 6 | 37 | 1 | 4 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0005c0005t0001 | 0/1 | 1829 | 22 | 4 | 7 | 5 | 3 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0005c0036t0001 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0006c0006t0001 | 0/0 | 1829 | 17 | 2 | 6 | 8 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0007c0007t0001 | 1/0 | 1829 | 14 | 13 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0008c0012t0001 | 0/0 | 1829 | 3 | 3 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0008c0027t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0009c0010t0001 | 0/0 | 1829 | 4 | 3 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0010c0009t0001 | 0/0 | 1829 | 4 | 2 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0011c0015t0001 | 0/0 | 1829 | 3 | 0 | 2 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0012c0014t0001 | 0/0 | 1829 | 3 | 0 | 0 | 1 | 0 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0013c0011t0001 | 0/0 | 1829 | 3 | 0 | 0 | 3 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0014c0023t0001 | 0/0 | 1829 | 2 | 0 | 1 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0015c0024t0001 | 0/0 | 1829 | 2 | 0 | 0 | 0 | 0 | 2 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0016c0016t0001 | 0/0 | 1829 | 2 | 1 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0017c0020t0001 | 0/0 | 1829 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0018c0021t0001 | 0/0 | 1829 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0019c0022t0001 | 0/0 | 1829 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0020c0019t0001 | 0/0 | 1829 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0021c0018t0001 | 0/0 | 1829 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0022c0032t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0023c0033t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0024c0029t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0025c0030t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0026c0031t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0027c0034t0001 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0028c0028t0001 | 0/0 | 1829 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0029c0026t0001 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0030c0037t0001 | 0/0 | 1829 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0031c0025t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| a0032c0038t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | copy fasta | chr1 | 207640133 | 207728703 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0013t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0013t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0017t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0001c0017t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0002c0035t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0008t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0008t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0008t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0008t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0003c0008t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0004c0004t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0030 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0005c0036t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0006c0006t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0007c0007t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0008c0012t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0008c0012t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0008c0012t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0008c0027t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0009c0010t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0009c0010t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0009c0010t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0009c0010t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0010c0009t0001g0001 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0011c0015t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0011c0015t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0011c0015t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0012c0014t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0012c0014t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0012c0014t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0013c0011t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0013c0011t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0013c0011t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0014c0023t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0014c0023t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0015c0024t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0015c0024t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0016c0016t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0016c0016t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0017c0020t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0017c0020t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0018c0021t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0018c0021t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0019c0022t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0019c0022t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0020c0019t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0020c0019t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0021c0018t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0021c0018t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0022c0032t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0023c0033t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0024c0029t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0025c0030t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0026c0031t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0027c0034t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0028c0028t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0029c0026t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0030c0037t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0031c0025t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| a0032c0038t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0005 | t0001 | g0031 | EUR | GBR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0240 | EUR | GBR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0105 | EUR | GBR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00140 | hp2 | a0006 | c0006 | t0001 | g0069 | EUR | GBR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00280 | hp1 | a0005 | c0005 | t0001 | g0039 | EUR | FIN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00280 | hp2 | a0004 | c0004 | t0001 | g0296 | EUR | FIN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00323 | hp1 | a0005 | c0005 | t0001 | g0040 | EUR | FIN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0230 | EUR | FIN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00408 | hp1 | a0005 | c0005 | t0001 | g0024 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00423 | hp1 | a0005 | c0005 | t0001 | g0026 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00423 | hp2 | a0017 | c0020 | t0001 | g0055 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00558 | hp2 | a0027 | c0034 | t0001 | g0315 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00597 | hp1 | a0004 | c0004 | t0001 | g0314 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00609 | hp1 | a0006 | c0006 | t0001 | g0082 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00609 | hp2 | a0004 | c0004 | t0001 | g0272 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0241 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0229 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00673 | hp1 | a0004 | c0004 | t0001 | g0271 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | CHS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0181 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00735 | hp2 | a0006 | c0006 | t0001 | g0108 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0221 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0177 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01069 | hp1 | a0010 | c0009 | t0001 | g0001 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0224 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0242 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01071 | hp1 | a0010 | c0009 | t0001 | g0001 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01081 | hp1 | a0005 | c0005 | t0001 | g0035 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0246 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01099 | hp2 | a0006 | c0006 | t0001 | g0104 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01106 | hp1 | a0011 | c0015 | t0001 | g0037 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01106 | hp2 | a0006 | c0006 | t0001 | g0064 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01109 | hp1 | a0016 | c0016 | t0001 | g0124 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01109 | hp2 | a0009 | c0010 | t0001 | g0328 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01167 | hp1 | a0005 | c0005 | t0001 | g0018 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01167 | hp2 | a0006 | c0006 | t0001 | g0109 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01168 | hp1 | a0003 | c0008 | t0001 | g0225 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01168 | hp2 | a0004 | c0004 | t0001 | g0014 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01169 | hp1 | a0006 | c0006 | t0001 | g0110 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01169 | hp2 | a0004 | c0004 | t0001 | g0014 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0121 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01192 | hp1 | a0005 | c0005 | t0001 | g0028 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01255 | hp1 | a0005 | c0005 | t0001 | g0017 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0259 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01256 | hp2 | a0004 | c0004 | t0001 | g0274 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01257 | hp1 | a0004 | c0004 | t0001 | g0295 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01258 | hp1 | a0004 | c0004 | t0001 | g0320 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01261 | hp2 | a0005 | c0005 | t0001 | g0034 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01346 | hp1 | a0011 | c0015 | t0001 | g0016 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0128 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01358 | hp1 | a0005 | c0005 | t0001 | g0027 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0190 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01433 | hp2 | a0005 | c0005 | t0001 | g0019 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0227 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | CLM | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0226 | EUR | IBS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0007 | EUR | IBS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0007 | EUR | IBS | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01891 | hp1 | a0005 | c0005 | t0001 | g0020 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0123 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0157 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01934 | hp2 | a0004 | c0004 | t0001 | g0286 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0161 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0216 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0006 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01978 | hp1 | a0006 | c0006 | t0001 | g0088 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01981 | hp1 | a0014 | c0023 | t0001 | g0257 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01981 | hp2 | a0021 | c0018 | t0001 | g0205 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG01993 | hp2 | a0003 | c0003 | t0001 | g0206 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0247 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02004 | hp2 | a0028 | c0028 | t0001 | g0189 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02015 | hp1 | a0006 | c0006 | t0001 | g0061 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02015 | hp2 | a0004 | c0004 | t0001 | g0305 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02040 | hp2 | a0004 | c0004 | t0001 | g0294 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02055 | hp1 | a0007 | c0007 | t0001 | g0126 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02071 | hp2 | a0003 | c0003 | t0001 | g0117 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02135 | hp1 | a0004 | c0004 | t0001 | g0298 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | CDX | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02155 | hp2 | a0004 | c0004 | t0001 | g0291 | EAS | CDX | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02257 | hp1 | a0019 | c0022 | t0001 | g0265 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02258 | hp1 | a0007 | c0007 | t0001 | g0131 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02258 | hp2 | a0007 | c0007 | t0001 | g0281 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0164 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02293 | hp1 | a0021 | c0018 | t0001 | g0217 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0180 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0122 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02615 | hp1 | a0032 | c0038 | t0001 | g0173 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02622 | hp2 | a0007 | c0007 | t0001 | g0275 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02630 | hp1 | a0001 | c0017 | t0001 | g0170 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02630 | hp2 | a0007 | c0007 | t0001 | g0277 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02647 | hp1 | a0010 | c0009 | t0001 | g0001 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02647 | hp2 | a0008 | c0012 | t0001 | g0234 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02723 | hp1 | a0031 | c0025 | t0001 | g0062 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02809 | hp1 | a0006 | c0006 | t0001 | g0233 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02809 | hp2 | a0026 | c0031 | t0001 | g0263 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02818 | hp1 | a0007 | c0007 | t0001 | g0276 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02897 | hp1 | a0008 | c0027 | t0001 | g0169 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02897 | hp2 | a0007 | c0007 | t0001 | g0322 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02922 | hp1 | a0007 | c0007 | t0001 | g0168 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02965 | hp1 | a0007 | c0007 | t0001 | g0129 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02970 | hp2 | a0008 | c0012 | t0001 | g0235 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02976 | hp1 | a0007 | c0007 | t0001 | g0130 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02976 | hp2 | a0019 | c0022 | t0001 | g0174 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0220 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03041 | hp1 | a0007 | c0007 | t0001 | g0178 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | GWD | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03098 | hp1 | a0005 | c0005 | t0001 | g0021 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03098 | hp2 | a0001 | c0017 | t0001 | g0125 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03130 | hp2 | a0018 | c0021 | t0001 | g0268 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03195 | hp1 | a0024 | c0029 | t0001 | g0041 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03209 | hp1 | a0009 | c0010 | t0001 | g0133 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03209 | hp2 | a0006 | c0006 | t0001 | g0327 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03225 | hp1 | a0004 | c0004 | t0001 | g0321 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03225 | hp2 | a0010 | c0009 | t0001 | g0001 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03239 | hp1 | a0011 | c0015 | t0001 | g0032 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03453 | hp1 | a0009 | c0010 | t0001 | g0132 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03486 | hp1 | a0025 | c0030 | t0001 | g0118 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03486 | hp2 | a0009 | c0010 | t0001 | g0120 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03490 | hp2 | a0012 | c0014 | t0001 | g0096 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0239 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03492 | hp2 | a0012 | c0014 | t0001 | g0097 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03516 | hp1 | a0018 | c0021 | t0001 | g0266 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03516 | hp2 | a0007 | c0007 | t0001 | g0119 | AFR | ESN | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03654 | hp1 | a0005 | c0005 | t0001 | g0038 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0150 | SAS | STU | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03688 | hp2 | a0030 | c0037 | t0001 | g0283 | SAS | STU | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03704 | hp1 | a0004 | c0004 | t0001 | g0301 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03704 | hp2 | a0015 | c0024 | t0001 | g0260 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03710 | hp2 | a0014 | c0023 | t0001 | g0261 | SAS | PJL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03831 | hp2 | a0005 | c0005 | t0001 | g0036 | SAS | BEB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | BEB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03927 | hp2 | a0004 | c0004 | t0001 | g0285 | SAS | BEB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0135 | SAS | BEB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03942 | hp2 | a0004 | c0004 | t0001 | g0292 | SAS | BEB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0092 | SAS | BEB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG04199 | hp1 | a0004 | c0004 | t0001 | g0284 | SAS | STU | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18522 | hp1 | a0016 | c0016 | t0001 | g0166 | AFR | YRI | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18612 | hp1 | a0004 | c0004 | t0001 | g0299 | EAS | CHB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18612 | hp2 | a0002 | c0035 | t0001 | g0046 | EAS | CHB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | CHB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | CHB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | YRI | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18939 | hp1 | a0006 | c0006 | t0001 | g0111 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18939 | hp2 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18941 | hp1 | a0004 | c0004 | t0001 | g0114 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18942 | hp1 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18944 | hp1 | a0004 | c0004 | t0001 | g0300 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18945 | hp1 | a0006 | c0006 | t0001 | g0060 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18946 | hp2 | a0004 | c0004 | t0001 | g0307 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18947 | hp1 | a0001 | c0013 | t0001 | g0011 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18947 | hp2 | a0017 | c0020 | t0001 | g0063 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18952 | hp2 | a0004 | c0004 | t0001 | g0312 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18954 | hp1 | a0012 | c0014 | t0001 | g0093 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18956 | hp2 | a0006 | c0006 | t0001 | g0058 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18959 | hp2 | a0004 | c0004 | t0001 | g0308 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18960 | hp1 | a0004 | c0004 | t0001 | g0288 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18960 | hp2 | a0003 | c0008 | t0001 | g0196 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18962 | hp2 | a0004 | c0004 | t0001 | g0287 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18963 | hp2 | a0013 | c0011 | t0001 | g0140 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18964 | hp2 | a0004 | c0004 | t0001 | g0290 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18965 | hp1 | a0006 | c0006 | t0001 | g0056 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18968 | hp2 | a0004 | c0004 | t0001 | g0289 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18969 | hp1 | a0004 | c0004 | t0001 | g0310 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18971 | hp1 | a0020 | c0019 | t0001 | g0163 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18971 | hp2 | a0029 | c0026 | t0001 | g0317 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18972 | hp1 | a0004 | c0004 | t0001 | g0319 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18975 | hp1 | a0004 | c0004 | t0001 | g0309 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18977 | hp1 | a0004 | c0004 | t0001 | g0313 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18977 | hp2 | a0003 | c0008 | t0001 | g0142 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18978 | hp1 | a0004 | c0004 | t0001 | g0311 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18981 | hp1 | a0004 | c0004 | t0001 | g0324 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18984 | hp2 | a0004 | c0004 | t0001 | g0293 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18985 | hp2 | a0003 | c0008 | t0001 | g0194 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18988 | hp2 | a0003 | c0008 | t0001 | g0188 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18989 | hp1 | a0013 | c0011 | t0001 | g0199 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18994 | hp1 | a0005 | c0005 | t0001 | g0022 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18995 | hp1 | a0013 | c0011 | t0001 | g0145 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18998 | hp1 | a0004 | c0004 | t0001 | g0325 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18999 | hp1 | a0005 | c0005 | t0001 | g0025 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA18999 | hp2 | a0006 | c0006 | t0001 | g0099 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19002 | hp1 | a0001 | c0013 | t0001 | g0011 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19002 | hp2 | a0004 | c0004 | t0001 | g0302 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19004 | hp1 | a0004 | c0004 | t0001 | g0273 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19005 | hp1 | a0020 | c0019 | t0001 | g0147 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19010 | hp1 | a0005 | c0036 | t0001 | g0015 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19012 | hp2 | a0004 | c0004 | t0001 | g0304 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19043 | hp1 | a0023 | c0033 | t0001 | g0269 | AFR | LWK | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | LWK | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19062 | hp2 | a0001 | c0013 | t0001 | g0197 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19063 | hp1 | a0004 | c0004 | t0001 | g0306 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19065 | hp1 | a0006 | c0006 | t0001 | g0089 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19066 | hp1 | a0005 | c0005 | t0001 | g0023 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19066 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19067 | hp2 | a0004 | c0004 | t0001 | g0303 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19070 | hp1 | a0004 | c0004 | t0001 | g0316 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19075 | hp2 | a0004 | c0004 | t0001 | g0326 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19077 | hp1 | a0004 | c0004 | t0001 | g0297 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19079 | hp1 | a0004 | c0004 | t0001 | g0318 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19085 | hp2 | a0004 | c0004 | t0001 | g0323 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0116 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | YRI | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0243 | EUR | TSI | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0192 | EUR | TSI | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA20905 | hp1 | a0015 | c0024 | t0001 | g0262 | SAS | GIH | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0228 | SAS | GIH | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02109 | hp1 | a0022 | c0032 | t0001 | g0270 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02109 | hp2 | a0007 | c0007 | t0001 | g0279 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0153 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02486 | hp2 | a0005 | c0005 | t0001 | g0033 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG06807 | hp1 | a0008 | c0012 | t0001 | g0179 | AFR | USA | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| HG06807 | hp2 | a0005 | c0005 | t0001 | g0029 | AFR | USA | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| homoSapiens_chm13v2 | hp1 | a0005 | c0005 | t0001 | g0030 | REF | REF | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| homoSapiens_grch38 | hp1 | a0007 | c0007 | t0001 | g0244 | REF | REF | CR1L_chr1_207640133_207728703 | CR1L | chr1 | 207640133 | 207728703 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:207645313
|
T | G | 1 | a0010 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
missense_variant | MODERATE | c.80T>G | p.Leu27Arg | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/12 | 181/1829 | 80/1710 | 27/569 | chr1 | 207645313 | ||
| chr1:207645325
|
T | C | 1 | a0013 | 3 | NA18963.hp2 NA18989.hp1 NA18995.hp1 |
missense_variant | MODERATE | c.92T>C | p.Phe31Ser | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/12 | 193/1829 | 92/1710 | 31/569 | chr1 | 207645325 | ||
| chr1:207677415
|
C | T | 1 | a0032 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.124C>T | p.Pro42Ser | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/12 | 225/1829 | 124/1710 | 42/569 | chr1 | 207677415 | ||
| chr1:207677419
|
T | C | 1 | a0031 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.128T>C | p.Phe43Ser | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/12 | 229/1829 | 128/1710 | 43/569 | chr1 | 207677419 | ||
| chr1:207677446
|
A | T | 1 | a0030 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.155A>T | p.Asp52Val | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/12 | 256/1829 | 155/1710 | 52/569 | chr1 | 207677446 | ||
| chr1:207677449
|
T | C | 1 | a0029 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.158T>C | p.Phe53Ser | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/12 | 259/1829 | 158/1710 | 53/569 | chr1 | 207677449 | ||
| chr1:207678209
|
C | T | 2 | a0014a0015 | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
missense_variant | MODERATE | c.289C>T | p.Arg97Cys | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/12 | 390/1829 | 289/1710 | 97/569 | chr1 | 207678209 | ||
| chr1:207678210
|
G | A | 1 | a0016 | 2 | HG01109.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.290G>A | p.Arg97His | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/12 | 391/1829 | 290/1710 | 97/569 | chr1 | 207678210 | ||
| chr1:207678266
|
A | G | 23 | a0002a0004a0005others(20): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
missense_variant | MODERATE | c.346A>G | p.Arg116Gly | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/12 | 447/1829 | 346/1710 | 116/569 | chr1 | 207678266 | ||
| chr1:207683909
|
A | G | 6 | a0004a0014a0015others(3): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
missense_variant | MODERATE | c.415A>G | p.Ile139Val | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/12 | 516/1829 | 415/1710 | 139/569 | chr1 | 207683909 | ||
| chr1:207694425
|
A | G | 2 | a0022a0023 | 2 | HG02109.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.536A>G | p.Tyr179Cys | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/12 | 637/1829 | 536/1710 | 179/569 | chr1 | 207694425 | ||
| chr1:207694509
|
G | A | 2 | a0014a0015 | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
missense_variant | MODERATE | c.620G>A | p.Cys207Tyr | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/12 | 721/1829 | 620/1710 | 207/569 | chr1 | 207694509 | ||
| chr1:207694544
|
G | A | 1 | a0031 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.655G>A | p.Gly219Ser | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/12 | 756/1829 | 655/1710 | 219/569 | chr1 | 207694544 | ||
| chr1:207694551
|
C | T | 5 | a0018a0019a0022others(2): Show | 7 | HG02109.hp1 HG02257.hp1 HG02809.hp2 others(4): Show |
missense_variant | MODERATE | c.662C>T | p.Ala221Val | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/12 | 763/1829 | 662/1710 | 221/569 | chr1 | 207694551 | ||
| chr1:207694677
|
G | T | 2 | a0014a0015 | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
missense_variant | MODERATE | c.788G>T | p.Gly263Val | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/12 | 889/1829 | 788/1710 | 263/569 | chr1 | 207694677 | ||
| chr1:207697810
|
G | A | 1 | a0024 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1079G>A | p.Gly360Asp | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/12 | 1180/1829 | 1079/1710 | 360/569 | chr1 | 207697810 | ||
| chr1:207699229
|
G | T | 2 | a0019a0026 | 3 | HG02257.hp1 HG02809.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.1183G>T | p.Ala395Ser | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/12 | 1284/1829 | 1183/1710 | 395/569 | chr1 | 207699229 | ||
| chr1:207699250
|
A | G | 4 | a0005a0011a0022others(1): Show | 28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
missense_variant | MODERATE | c.1204A>G | p.Asn402Asp | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/12 | 1305/1829 | 1204/1710 | 402/569 | chr1 | 207699250 | ||
| chr1:207701581
|
C | T | 3 | a0018a0019a0026 | 5 | HG02257.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.1291C>T | p.His431Tyr | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/12 | 1392/1829 | 1291/1710 | 431/569 | chr1 | 207701581 | ||
| chr1:207701583
|
T | G | 1 | a0021 | 2 | HG01981.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.1293T>G | p.His431Gln | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/12 | 1394/1829 | 1293/1710 | 431/569 | chr1 | 207701583 | ||
| chr1:207708212
|
A | G | 22 | a0001a0002a0004others(19): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
missense_variant | MODERATE | c.1363A>G | p.Ile455Val | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/12 | 1464/1829 | 1363/1710 | 455/569 | chr1 | 207708212 | ||
| chr1:207717473
|
G | A | 3 | a0009a0019a0023 | 7 | HG01109.hp2 HG02257.hp1 HG02976.hp2 others(4): Show |
missense_variant | MODERATE | c.1424G>A | p.Cys475Tyr | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/12 | 1525/1829 | 1424/1710 | 475/569 | chr1 | 207717473 | ||
| chr1:207717521
|
T | C | 9 | a0003a0006a0008others(6): Show | 88 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(85): Show |
missense_variant | MODERATE | c.1472T>C | p.Leu491Pro | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/12 | 1573/1829 | 1472/1710 | 491/569 | chr1 | 207717521 | ||
| chr1:207717547
|
G | A | 3 | a0012a0014a0028 | 6 | HG01981.hp1 HG02004.hp2 HG03490.hp2 others(3): Show |
missense_variant | MODERATE | c.1498G>A | p.Val500Ile | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/12 | 1599/1829 | 1498/1710 | 500/569 | chr1 | 207717547 | ||
| chr1:207717667
|
C | T | 2 | a0020a0031 | 3 | HG02723.hp1 NA18971.hp1 NA19005.hp1 |
missense_variant | MODERATE | c.1618C>T | p.Arg540Cys | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/12 | 1719/1829 | 1618/1710 | 540/569 | chr1 | 207717667 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:207677534
|
C | T | 3 | a0005c0005a0005c0036a0011c0015 | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
synonymous_variant | LOW | c.243C>T | p.Asn81Asn | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/12 | 344/1829 | 243/1710 | 81/569 | chr1 | 207677534 | ||
| chr1:207683881
|
C | T | 1 | a0002c0035 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.387C>T | p.Leu129Leu | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/12 | 488/1829 | 387/1710 | 129/569 | chr1 | 207683881 | ||
| chr1:207694543
|
T | C | 1 | a0005c0036 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.654T>C | p.Ser218Ser | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/12 | 755/1829 | 654/1710 | 218/569 | chr1 | 207694543 | ||
| chr1:207697606
|
C | T | 2 | a0001c0013a0003c0008 | 8 | HG01168.hp1 NA18947.hp1 NA18960.hp2 others(5): Show |
synonymous_variant | LOW | c.966C>T | p.Tyr322Tyr | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 6/12 | 1067/1829 | 966/1710 | 322/569 | chr1 | 207697606 | ||
| chr1:207697630
|
G | A | 2 | a0001c0017a0008c0027 | 3 | HG02630.hp1 HG02897.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.990G>A | p.Leu330Leu | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 6/12 | 1091/1829 | 990/1710 | 330/569 | chr1 | 207697630 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:207645374
|
G | A | 102 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(99): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.97+44G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645374 | ||||||
| chr1:207645484
|
C | A | 1 | a0004c0004t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.97+154C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645484 | ||||||
| chr1:207645494
|
T | A | 1 | a0005c0036t0001g0015 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.97+164T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645494 | ||||||
| chr1:207645655
|
G | A | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.97+325G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645655 | ||||||
| chr1:207645786
|
C | T | 1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.97+456C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645786 | ||||||
| chr1:207645814
|
G | T | 172 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(169): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.97+484G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645814 | ||||||
| chr1:207645858
|
G | A | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97+528G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645858 | ||||||
| chr1:207645883
|
C | G | 3 | a0014c0023t0001g0261a0015c0024t0001g0260a0015c0024t0001g0262 | 3 | HG03704.hp2 HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.97+553C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645883 | ||||||
| chr1:207645895
|
A | C | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.97+565A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645895 | ||||||
| chr1:207645903
|
T | C | 1 | a0002c0002t0001g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97+573T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207645903 | ||||||
| chr1:207646056
|
C | T | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.97+726C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646056 | ||||||
| chr1:207646125
|
G | A | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+795G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646125 | ||||||
| chr1:207646147
|
A | G | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97+817A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646147 | ||||||
| chr1:207646173
|
C | G | 1 | a0003c0003t0001g0259 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.97+843C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646173 | ||||||
| chr1:207646205
|
G | C | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+875G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646205 | ||||||
| chr1:207646230
|
G | C | 1 | a0002c0002t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.97+900G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646230 | ||||||
| chr1:207646384
|
T | C | 163 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(160): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.97+1054T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646384 | ||||||
| chr1:207646394
|
T | C | 2 | a0003c0003t0001g0116a0003c0003t0001g0117 | 2 | HG02071.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.97+1064T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646394 | ||||||
| chr1:207646446
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.97+1116C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646446 | ||||||
| chr1:207646506
|
T | C | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97+1176T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646506 | ||||||
| chr1:207646594
|
C | G | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97+1264C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646594 | ||||||
| chr1:207646710
|
C | CA | 62 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(59): Show | 68 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.97+1405dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207646710 | |||||
| chr1:207646710
|
C | CAA | 53 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0137others(50): Show | 54 | HG00438.hp2 HG01255.hp2 HG01256.hp1 others(51): Show |
intron_variant | MODIFIER | c.97+1404_97+1405dup others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207646710 | |||||
| chr1:207646710
|
C | CAAA | 9 | a0001c0017t0001g0125a0002c0002t0001g0127a0003c0003t0001g0121others(6): Show | 9 | HG01109.hp1 HG01175.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+1403_97+1405dup others(3): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207646710 | |||||
| chr1:207646710
|
CA | C | 67 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(64): Show | 70 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.97+1405delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207646710 | |||||
| chr1:207646710
|
CAA | C | 81 | a0002c0002t0001g0042a0002c0002t0001g0065a0002c0002t0001g0066others(78): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.97+1404_97+1405del others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207646710 | |||||
| chr1:207646710
|
CAAA | C | 7 | a0002c0002t0001g0005a0002c0002t0001g0112a0002c0002t0001g0113others(4): Show | 8 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+1403_97+1405del others(3): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207646710 | |||||
| chr1:207646856
|
G | A | 172 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(169): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.97+1526G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646856 | ||||||
| chr1:207646933
|
A | G | 192 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(189): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.97+1603A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646933 | ||||||
| chr1:207646968
|
A | G | 192 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(189): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.97+1638A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207646968 | ||||||
| chr1:207647022
|
TAC | T | 112 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(109): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.97+1699_97+1700del others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207647022 | |||||
| chr1:207647030
|
C | A | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.97+1700C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647030 | ||||||
| chr1:207647056
|
CT | C | 20 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(17): Show | 20 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+1733delT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207647056 | |||||
| chr1:207647144
|
A | G | 1 | a0002c0002t0001g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.97+1814A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647144 | ||||||
| chr1:207647267
|
A | G | 21 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(18): Show | 21 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.97+1937A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647267 | ||||||
| chr1:207647390
|
G | A | 2 | a0010c0009t0001g0001a0031c0025t0001g0062 | 5 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+2060G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647390 | ||||||
| chr1:207647480
|
C | A | 1 | a0003c0003t0001g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.97+2150C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647480 | ||||||
| chr1:207647489
|
T | C | 3 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+2159T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647489 | ||||||
| chr1:207647515
|
G | A | 1 | a0003c0003t0001g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.97+2185G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647515 | ||||||
| chr1:207647650
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+2320G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647650 | ||||||
| chr1:207647696
|
G | A | 6 | a0001c0001t0001g0278a0007c0007t0001g0275a0007c0007t0001g0276others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+2366G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647696 | ||||||
| chr1:207647701
|
A | G | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(91): Show | 101 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.97+2371A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647701 | ||||||
| chr1:207647934
|
G | T | 7 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(4): Show | 7 | HG01496.hp2 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+2604G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207647934 | ||||||
| chr1:207648052
|
T | C | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.97+2722T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648052 | ||||||
| chr1:207648084
|
G | T | 1 | a0004c0004t0001g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.97+2754G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648084 | ||||||
| chr1:207648174
|
A | AAC | 7 | a0001c0001t0001g0231a0004c0004t0001g0274a0004c0004t0001g0320others(4): Show | 7 | HG01256.hp2 HG01258.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+2874_97+2875dup others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648174 | |||||
| chr1:207648174
|
A | AACAC | 5 | a0004c0004t0001g0014a0004c0004t0001g0318a0004c0004t0001g0319others(2): Show | 6 | HG01168.hp2 HG01169.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+2872_97+2875dup others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648174 | |||||
| chr1:207648174
|
A | AACACAC | 33 | a0004c0004t0001g0013a0004c0004t0001g0114a0004c0004t0001g0271others(30): Show | 34 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.97+2870_97+2875dup others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648174 | |||||
| chr1:207648174
|
A | AACACACA others(1): Show |
8 | a0004c0004t0001g0285a0004c0004t0001g0286a0004c0004t0001g0287others(5): Show | 8 | HG01934.hp2 HG02155.hp2 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+2868_97+2875dup others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648174 | |||||
| chr1:207648174
|
A | ACACACAC others(4): Show |
1 | a0002c0002t0001g0176 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.97+2844_97+2845ins others(11): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648174 | ||||||
| chr1:207648174
|
AACAC | A | 102 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 111 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.97+2872_97+2875del others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648174 | |||||
| chr1:207648174
|
AACACAC | A | 3 | a0006c0006t0001g0064a0017c0020t0001g0063a0022c0032t0001g0270 | 3 | HG01106.hp2 HG02109.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.97+2870_97+2875del others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648174 | |||||
| chr1:207648196
|
CACACACA others(3): Show |
C | 3 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+2876_97+2885del others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648196 | |||||
| chr1:207648198
|
CACACACA others(1): Show |
C | 68 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(65): Show | 70 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.97+2876_97+2883del others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648198 | |||||
| chr1:207648200
|
CACACAG | C | 37 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(34): Show | 40 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.97+2876_97+2881del others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648200 | |||||
| chr1:207648202
|
C | CACACACA others(7): Show |
1 | a0015c0024t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.97+2875_97+2876ins others(14): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648202 | |||||
| chr1:207648202
|
C | CACACACA others(5): Show |
1 | a0015c0024t0001g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.97+2875_97+2876ins others(12): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648202 | |||||
| chr1:207648206
|
G | C | 18 | a0001c0001t0001g0167a0001c0017t0001g0125a0001c0017t0001g0170others(15): Show | 18 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+2876G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648206 | ||||||
| chr1:207648208
|
C | CACACACA others(3): Show |
4 | a0002c0002t0001g0115a0002c0002t0001g0172a0019c0022t0001g0174others(1): Show | 4 | HG01884.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+2887_97+2888ins others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648208 | |||||
| chr1:207648208
|
C | CACACACA others(1): Show |
4 | a0002c0002t0001g0127a0002c0002t0001g0175a0016c0016t0001g0124others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+2885_97+2886ins others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648208 | |||||
| chr1:207648208
|
C | CAG | 6 | a0001c0001t0001g0167a0001c0017t0001g0125a0001c0017t0001g0170others(3): Show | 6 | HG02055.hp1 HG02630.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+2879_97+2880ins others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648208 | |||||
| chr1:207648208
|
C | G | 110 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(107): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.97+2878C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648208 | ||||||
| chr1:207648221
|
ACAG | A | 8 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(5): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+2892_97+2894del others(3): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648221 | ||||||
| chr1:207648222
|
C | G | 8 | a0001c0001t0001g0171a0005c0005t0001g0018a0006c0006t0001g0064others(5): Show | 8 | HG01106.hp2 HG01167.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+2892C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648222 | ||||||
| chr1:207648223
|
AG | A | 5 | a0001c0001t0001g0171a0005c0005t0001g0018a0006c0006t0001g0064others(2): Show | 5 | HG01106.hp2 HG01167.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+2894delG | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648223 | ||||||
| chr1:207648224
|
G | A | 4 | a0004c0004t0001g0285a0014c0023t0001g0257a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+2894G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648224 | ||||||
| chr1:207648224
|
GA | G | 57 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0152others(54): Show | 61 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.97+2908delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648224 | |||||
| chr1:207648225
|
A | G | 8 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(5): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+2895A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648225 | ||||||
| chr1:207648226
|
A | G | 1 | a0026c0031t0001g0263 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.97+2896A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648226 | ||||||
| chr1:207648235
|
A | AC | 15 | a0001c0001t0001g0167a0001c0017t0001g0125a0001c0017t0001g0170others(12): Show | 15 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.97+2905_97+2906ins others(1): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648235 | ||||||
| chr1:207648235
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97+2905A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648235 | ||||||
| chr1:207648324
|
A | G | 1 | a0002c0002t0001g0106 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.97+2994A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648324 | ||||||
| chr1:207648373
|
A | G | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+3043A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648373 | ||||||
| chr1:207648379
|
TTAAATCA others(16): Show |
T | 8 | a0001c0001t0001g0010a0001c0001t0001g0248a0001c0001t0001g0249others(5): Show | 9 | HG01192.hp2 HG02257.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+3052_97+3074del others(23): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648379 | |||||
| chr1:207648465
|
C | T | 2 | a0003c0003t0001g0181a0003c0003t0001g0247 | 2 | HG00735.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.97+3135C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648465 | ||||||
| chr1:207648564
|
T | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0258 | 3 | HG02257.hp2 HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.97+3234T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648564 | ||||||
| chr1:207648587
|
CAT | C | 144 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0203others(141): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.97+3258_97+3259del others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648587 | ||||||
| chr1:207648733
|
G | A | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+3403G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648733 | ||||||
| chr1:207648771
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.97+3441A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648771 | ||||||
| chr1:207648952
|
C | T | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+3622C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648952 | ||||||
| chr1:207648958
|
G | A | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+3628G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648958 | ||||||
| chr1:207648965
|
AT | A | 20 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(17): Show | 20 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+3642delT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207648965 | |||||
| chr1:207648974
|
A | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+3644A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207648974 | ||||||
| chr1:207649031
|
A | G | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.97+3701A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649031 | ||||||
| chr1:207649088
|
T | A | 1 | a0001c0001t0001g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+3758T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649088 | ||||||
| chr1:207649121
|
A | G | 1 | a0004c0004t0001g0292 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.97+3791A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649121 | ||||||
| chr1:207649153
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+3823T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649153 | ||||||
| chr1:207649211
|
C | T | 7 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+3881C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649211 | ||||||
| chr1:207649236
|
G | T | 20 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(17): Show | 20 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+3906G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649236 | ||||||
| chr1:207649379
|
G | T | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+4049G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649379 | ||||||
| chr1:207649422
|
G | A | 193 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.97+4092G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649422 | ||||||
| chr1:207649451
|
T | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+4121T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649451 | ||||||
| chr1:207649511
|
G | A | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+4181G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649511 | ||||||
| chr1:207649750
|
T | C | 1 | a0001c0017t0001g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97+4420T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649750 | ||||||
| chr1:207649816
|
T | C | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+4486T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649816 | ||||||
| chr1:207649895
|
A | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+4565A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649895 | ||||||
| chr1:207649903
|
C | T | 20 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(17): Show | 20 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+4573C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207649903 | ||||||
| chr1:207650005
|
G | C | 1 | a0007c0007t0001g0281 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.97+4675G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650005 | ||||||
| chr1:207650060
|
C | T | 113 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.97+4730C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650060 | ||||||
| chr1:207650066
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.97+4736T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650066 | ||||||
| chr1:207650111
|
G | C | 1 | a0021c0018t0001g0205 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.97+4781G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650111 | ||||||
| chr1:207650419
|
G | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+5089G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650419 | ||||||
| chr1:207650520
|
A | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+5190A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650520 | ||||||
| chr1:207650538
|
GAAATA | G | 6 | a0001c0001t0001g0171a0001c0017t0001g0125a0001c0017t0001g0170others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+5213_97+5217del others(5): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207650538 | |||||
| chr1:207650709
|
G | A | 2 | a0001c0001t0001g0280a0007c0007t0001g0281 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.97+5379G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650709 | ||||||
| chr1:207650788
|
ATT | A | 121 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(118): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.97+5472_97+5473del others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207650788 | |||||
| chr1:207650897
|
T | A | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+5567T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650897 | ||||||
| chr1:207650987
|
A | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+5657A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207650987 | ||||||
| chr1:207651008
|
A | G | 2 | a0022c0032t0001g0270a0023c0033t0001g0269 | 2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.97+5678A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651008 | ||||||
| chr1:207651031
|
C | G | 3 | a0002c0002t0001g0105a0006c0006t0001g0064a0006c0006t0001g0104 | 3 | HG00140.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.97+5701C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651031 | ||||||
| chr1:207651037
|
G | A | 43 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0152others(40): Show | 46 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.97+5707G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651037 | ||||||
| chr1:207651063
|
A | G | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+5733A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651063 | ||||||
| chr1:207651093
|
A | C | 20 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(17): Show | 20 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+5763A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651093 | ||||||
| chr1:207651193
|
G | A | 9 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+5863G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651193 | ||||||
| chr1:207651293
|
A | AATTC | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+5964_97+5965ins others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207651293 | |||||
| chr1:207651363
|
A | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+6033A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651363 | ||||||
| chr1:207651528
|
C | T | 1 | a0001c0017t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97+6198C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651528 | ||||||
| chr1:207651538
|
T | A | 2 | a0007c0007t0001g0126a0007c0007t0001g0168 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.97+6208T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651538 | ||||||
| chr1:207651659
|
G | GA | 17 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(14): Show | 17 | HG01109.hp1 HG01433.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.97+6339dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207651659 | |||||
| chr1:207651995
|
C | T | 1 | a0004c0004t0001g0291 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.97+6665C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207651995 | ||||||
| chr1:207652070
|
A | G | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.97+6740A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652070 | ||||||
| chr1:207652124
|
G | C | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+6794G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652124 | ||||||
| chr1:207652141
|
G | C | 1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.97+6811G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652141 | ||||||
| chr1:207652179
|
G | A | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+6849G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652179 | ||||||
| chr1:207652188
|
G | A | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.97+6858G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652188 | ||||||
| chr1:207652194
|
T | C | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+6864T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652194 | ||||||
| chr1:207652282
|
C | T | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+6952C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652282 | ||||||
| chr1:207652317
|
C | T | 4 | a0004c0004t0001g0287a0004c0004t0001g0288a0004c0004t0001g0289others(1): Show | 4 | NA18960.hp1 NA18962.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+6987C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652317 | ||||||
| chr1:207652412
|
G | A | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+7082G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652412 | ||||||
| chr1:207652414
|
A | G | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+7084A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652414 | ||||||
| chr1:207652452
|
A | G | 1 | a0003c0003t0001g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.97+7122A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652452 | ||||||
| chr1:207652460
|
T | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+7130T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652460 | ||||||
| chr1:207652749
|
C | A | 8 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0236others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+7419C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652749 | ||||||
| chr1:207652750
|
C | CT | 121 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(118): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.97+7430dupT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207652750 | |||||
| chr1:207652797
|
G | T | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+7467G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652797 | ||||||
| chr1:207652825
|
AT | A | 8 | a0005c0005t0001g0022a0005c0005t0001g0023a0005c0005t0001g0024others(5): Show | 8 | HG00408.hp1 HG00423.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+7504delT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207652825 | |||||
| chr1:207652889
|
A | T | 1 | a0006c0006t0001g0060 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.97+7559A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652889 | ||||||
| chr1:207652988
|
A | T | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+7658A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652988 | ||||||
| chr1:207652999
|
A | G | 9 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+7669A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207652999 | ||||||
| chr1:207653000
|
C | T | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97+7670C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653000 | ||||||
| chr1:207653256
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.97+7926C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653256 | ||||||
| chr1:207653350
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+8020G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653350 | ||||||
| chr1:207653431
|
G | A | 138 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(135): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.97+8101G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653431 | ||||||
| chr1:207653513
|
C | G | 113 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.97+8183C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653513 | ||||||
| chr1:207653705
|
G | A | 2 | a0004c0004t0001g0286a0004c0004t0001g0292 | 2 | HG01934.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.97+8375G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653705 | ||||||
| chr1:207653722
|
A | C | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+8392A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653722 | ||||||
| chr1:207653724
|
A | G | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+8394A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653724 | ||||||
| chr1:207653931
|
G | T | 1 | a0004c0004t0001g0290 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.97+8601G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207653931 | ||||||
| chr1:207654193
|
G | C | 122 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(119): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.97+8863G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207654193 | ||||||
| chr1:207654241
|
CTT | C | 5 | a0001c0017t0001g0125a0001c0017t0001g0170a0007c0007t0001g0126others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+8912_97+8913del others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207654241 | ||||||
| chr1:207654267
|
T | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+8937T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207654267 | ||||||
| chr1:207654286
|
G | A | 1 | a0001c0017t0001g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97+8956G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207654286 | ||||||
| chr1:207654453
|
T | C | 6 | a0001c0001t0001g0278a0007c0007t0001g0275a0007c0007t0001g0276others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+9123T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207654453 | ||||||
| chr1:207654590
|
T | C | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+9260T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207654590 | ||||||
| chr1:207654592
|
C | T | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+9262C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207654592 | ||||||
| chr1:207654950
|
C | A | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97+9620C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207654950 | ||||||
| chr1:207655138
|
T | C | 1 | a0030c0037t0001g0283 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.97+9808T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655138 | ||||||
| chr1:207655195
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+9865A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655195 | ||||||
| chr1:207655287
|
CT | C | 10 | a0001c0001t0001g0136a0001c0001t0001g0207a0001c0001t0001g0237others(7): Show | 10 | HG01070.hp2 HG01496.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+9973delT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207655287 | |||||
| chr1:207655362
|
A | G | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+10032A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655362 | ||||||
| chr1:207655407
|
G | A | 143 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(140): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.97+10077G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655407 | ||||||
| chr1:207655420
|
A | G | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+10090A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655420 | ||||||
| chr1:207655439
|
G | A | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+10109G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655439 | ||||||
| chr1:207655542
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0222 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.97+10212A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655542 | ||||||
| chr1:207655630
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+10300G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655630 | ||||||
| chr1:207655857
|
T | C | 1 | a0003c0003t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.97+10527T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655857 | ||||||
| chr1:207655875
|
C | T | 52 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0057others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.97+10545C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655875 | ||||||
| chr1:207655891
|
A | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+10561A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655891 | ||||||
| chr1:207655896
|
G | A | 2 | a0002c0002t0001g0070a0006c0006t0001g0069 | 2 | HG00140.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.97+10566G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655896 | ||||||
| chr1:207655964
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.97+10634C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207655964 | ||||||
| chr1:207656186
|
C | T | 2 | a0003c0003t0001g0165a0003c0003t0001g0247 | 2 | HG02004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.97+10856C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656186 | ||||||
| chr1:207656204
|
C | T | 24 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.97+10874C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656204 | ||||||
| chr1:207656239
|
A | AAATC | 62 | a0002c0002t0001g0264a0002c0002t0001g0267a0004c0004t0001g0013others(59): Show | 64 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.97+10935_97+10938d others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207656239 | |||||
| chr1:207656239
|
A | AAATCAAT others(1): Show |
1 | a0002c0002t0001g0003 | 3 | HG01891.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.97+10931_97+10938d others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207656239 | |||||
| chr1:207656276
|
C | T | 12 | a0002c0002t0001g0004a0002c0002t0001g0044a0002c0002t0001g0045others(9): Show | 13 | HG00558.hp1 HG00738.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.97+10946C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656276 | ||||||
| chr1:207656308
|
T | G | 123 | a0001c0001t0001g0167a0001c0001t0001g0278a0001c0001t0001g0280others(120): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.97+10978T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656308 | ||||||
| chr1:207656415
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+11085C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656415 | ||||||
| chr1:207656493
|
C | T | 2 | a0003c0003t0001g0229a0003c0003t0001g0230 | 2 | HG00323.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.97+11163C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656493 | ||||||
| chr1:207656495
|
A | C | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.97+11165A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656495 | ||||||
| chr1:207656579
|
A | G | 2 | a0007c0007t0001g0279a0007c0007t0001g0322 | 2 | HG02109.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.97+11249A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656579 | ||||||
| chr1:207656582
|
C | A | 1 | a0005c0005t0001g0023 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.97+11252C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656582 | ||||||
| chr1:207656689
|
G | C | 1 | a0002c0002t0001g0071 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.97+11359G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656689 | ||||||
| chr1:207656692
|
C | T | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+11362C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656692 | ||||||
| chr1:207656745
|
C | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+11415C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207656745 | ||||||
| chr1:207657038
|
T | C | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+11708T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657038 | ||||||
| chr1:207657193
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.97+11863G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657193 | ||||||
| chr1:207657432
|
G | T | 9 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+12102G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657432 | ||||||
| chr1:207657459
|
A | T | 16 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(13): Show | 16 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+12129A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657459 | ||||||
| chr1:207657535
|
A | G | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+12205A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657535 | ||||||
| chr1:207657559
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.97+12229A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657559 | ||||||
| chr1:207657578
|
T | C | 7 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+12248T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657578 | ||||||
| chr1:207657586
|
C | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+12256C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657586 | ||||||
| chr1:207657587
|
C | CA | 7 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(4): Show | 9 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+12265dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207657587 | |||||
| chr1:207657794
|
C | A | 7 | a0004c0004t0001g0014a0004c0004t0001g0274a0004c0004t0001g0286others(4): Show | 8 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+12464C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657794 | ||||||
| chr1:207657812
|
C | T | 1 | a0027c0034t0001g0315 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.97+12482C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657812 | ||||||
| chr1:207657985
|
C | T | 7 | a0001c0001t0001g0278a0001c0001t0001g0282a0007c0007t0001g0275others(4): Show | 7 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+12655C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207657985 | ||||||
| chr1:207658012
|
C | G | 112 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(109): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.97+12682C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207658012 | ||||||
| chr1:207658307
|
G | GAA | 287 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(284): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.97+12985_97+12986d others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207658307 | |||||
| chr1:207658307
|
G | GAAA | 22 | a0001c0001t0001g0167a0001c0001t0001g0171a0002c0002t0001g0003others(19): Show | 24 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.97+12984_97+12986d others(5): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207658307 | |||||
| chr1:207658324
|
G | A | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+12994G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207658324 | ||||||
| chr1:207658437
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0256 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.97+13107G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207658437 | ||||||
| chr1:207658449
|
C | T | 1 | a0014c0023t0001g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.97+13119C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207658449 | ||||||
| chr1:207658715
|
C | G | 1 | a0004c0004t0001g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.97+13385C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207658715 | ||||||
| chr1:207658740
|
C | A | 3 | a0002c0002t0001g0073a0002c0002t0001g0074a0002c0002t0001g0113 | 3 | HG02451.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.97+13410C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207658740 | ||||||
| chr1:207658757
|
C | T | 112 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(109): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.97+13427C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207658757 | ||||||
| chr1:207658808
|
C | T | 125 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(122): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.97+13478C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207658808 | ||||||
| chr1:207659057
|
G | A | 121 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(118): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.97+13727G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659057 | ||||||
| chr1:207659069
|
C | G | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.97+13739C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659069 | ||||||
| chr1:207659237
|
T | A | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97+13907T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659237 | ||||||
| chr1:207659271
|
G | C | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97+13941G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659271 | ||||||
| chr1:207659357
|
C | G | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97+14027C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659357 | ||||||
| chr1:207659383
|
G | A | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+14053G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659383 | ||||||
| chr1:207659466
|
T | G | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+14136T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659466 | ||||||
| chr1:207659631
|
G | C | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+14301G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659631 | ||||||
| chr1:207659669
|
C | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.97+14339C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659669 | ||||||
| chr1:207659956
|
G | A | 112 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(109): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.97+14626G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659956 | ||||||
| chr1:207659983
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0248a0001c0001t0001g0249others(5): Show | 9 | HG01192.hp2 HG02257.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+14653C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659983 | ||||||
| chr1:207659991
|
T | G | 129 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(126): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.97+14661T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207659991 | ||||||
| chr1:207660012
|
G | A | 103 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(100): Show | 110 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.97+14682G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660012 | ||||||
| chr1:207660080
|
C | T | 1 | a0002c0002t0001g0176 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.97+14750C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660080 | ||||||
| chr1:207660239
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.97+14909C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660239 | ||||||
| chr1:207660260
|
A | G | 1 | a0002c0002t0001g0103 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.97+14930A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660260 | ||||||
| chr1:207660330
|
G | A | 1 | a0003c0003t0001g0224 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.97+15000G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660330 | ||||||
| chr1:207660338
|
C | A | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+15008C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660338 | ||||||
| chr1:207660740
|
G | T | 7 | a0001c0001t0001g0278a0001c0001t0001g0282a0007c0007t0001g0275others(4): Show | 7 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+15410G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660740 | ||||||
| chr1:207660837
|
A | G | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+15507A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660837 | ||||||
| chr1:207660839
|
G | A | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97+15509G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660839 | ||||||
| chr1:207660895
|
G | A | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+15565G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660895 | ||||||
| chr1:207660922
|
C | T | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97+15592C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660922 | ||||||
| chr1:207660956
|
C | T | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+15626C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207660956 | ||||||
| chr1:207661028
|
T | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.97+15698T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661028 | ||||||
| chr1:207661031
|
C | G | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97+15701C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661031 | ||||||
| chr1:207661057
|
A | G | 3 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+15727A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661057 | ||||||
| chr1:207661179
|
A | G | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.97+15849A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661179 | ||||||
| chr1:207661204
|
A | G | 1 | a0003c0003t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.97+15874A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661204 | ||||||
| chr1:207661206
|
C | CTT | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+15878_97+15879d others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207661206 | |||||
| chr1:207661316
|
A | G | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.97+15986A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661316 | ||||||
| chr1:207661330
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.97+16000G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661330 | ||||||
| chr1:207661400
|
G | T | 1 | a0003c0003t0001g0117 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.98-15989G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661400 | ||||||
| chr1:207661491
|
T | A | 1 | a0004c0004t0001g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.98-15898T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661491 | ||||||
| chr1:207661516
|
C | T | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-15873C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661516 | ||||||
| chr1:207661599
|
T | A | 3 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-15790T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661599 | ||||||
| chr1:207661712
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-15677C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661712 | ||||||
| chr1:207661713
|
G | A | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-15676G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661713 | ||||||
| chr1:207661771
|
C | G | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-15618C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661771 | ||||||
| chr1:207661784
|
C | T | 1 | a0007c0007t0001g0281 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.98-15605C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661784 | ||||||
| chr1:207661793
|
CT | C | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-15593delT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207661793 | |||||
| chr1:207661847
|
A | C | 9 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-15542A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661847 | ||||||
| chr1:207661944
|
T | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-15445T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661944 | ||||||
| chr1:207661949
|
T | C | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-15440T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207661949 | ||||||
| chr1:207662014
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98-15375C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662014 | ||||||
| chr1:207662015
|
G | A | 1 | a0003c0003t0001g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.98-15374G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662015 | ||||||
| chr1:207662141
|
T | C | 193 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.98-15248T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662141 | ||||||
| chr1:207662218
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.98-15171C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662218 | ||||||
| chr1:207662301
|
G | C | 1 | a0009c0010t0001g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.98-15088G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662301 | ||||||
| chr1:207662342
|
A | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.98-15047A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662342 | ||||||
| chr1:207662389
|
G | C | 193 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.98-15000G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662389 | ||||||
| chr1:207662414
|
T | A | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-14975T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662414 | ||||||
| chr1:207662462
|
G | A | 8 | a0001c0001t0001g0278a0001c0001t0001g0282a0006c0006t0001g0327others(5): Show | 8 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.98-14927G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662462 | ||||||
| chr1:207662467
|
G | A | 73 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(70): Show | 75 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.98-14922G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662467 | ||||||
| chr1:207662526
|
G | A | 1 | a0002c0002t0001g0264 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.98-14863G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662526 | ||||||
| chr1:207662711
|
A | G | 14 | a0001c0001t0001g0183a0001c0001t0001g0207a0001c0001t0001g0218others(11): Show | 16 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.98-14678A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662711 | ||||||
| chr1:207662717
|
A | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.98-14672A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662717 | ||||||
| chr1:207662734
|
T | A | 193 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.98-14655T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662734 | ||||||
| chr1:207662967
|
T | C | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-14422T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207662967 | ||||||
| chr1:207663048
|
C | T | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-14341C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663048 | ||||||
| chr1:207663063
|
G | T | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-14326G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663063 | ||||||
| chr1:207663105
|
A | T | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-14284A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663105 | ||||||
| chr1:207663110
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.98-14279G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663110 | ||||||
| chr1:207663131
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.98-14258C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663131 | ||||||
| chr1:207663300
|
G | C | 1 | a0004c0004t0001g0295 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.98-14089G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663300 | ||||||
| chr1:207663335
|
C | A | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-14054C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663335 | ||||||
| chr1:207663348
|
C | A | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.98-14041C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663348 | ||||||
| chr1:207663348
|
C | T | 9 | a0001c0001t0001g0134a0007c0007t0001g0119a0007c0007t0001g0129others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-14041C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663348 | ||||||
| chr1:207663413
|
A | G | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.98-13976A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663413 | ||||||
| chr1:207663470
|
G | A | 2 | a0016c0016t0001g0124a0016c0016t0001g0166 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-13919G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663470 | ||||||
| chr1:207663586
|
A | C | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.98-13803A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663586 | ||||||
| chr1:207663635
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.98-13754G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663635 | ||||||
| chr1:207663644
|
A | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-13745A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663644 | ||||||
| chr1:207663717
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.98-13672C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663717 | ||||||
| chr1:207663719
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-13670C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663719 | ||||||
| chr1:207663743
|
AGCT | A | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.98-13644_98-13642d others(5): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207663743 | |||||
| chr1:207663756
|
C | T | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-13633C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663756 | ||||||
| chr1:207663832
|
C | T | 142 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(139): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.98-13557C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663832 | ||||||
| chr1:207663834
|
G | A | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.98-13555G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663834 | ||||||
| chr1:207663946
|
C | T | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.98-13443C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207663946 | ||||||
| chr1:207663981
|
CT | C | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-13401delT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207663981 | |||||
| chr1:207664013
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98-13376G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207664013 | ||||||
| chr1:207664145
|
T | C | 192 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(189): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.98-13244T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207664145 | ||||||
| chr1:207664202
|
A | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-13187A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207664202 | ||||||
| chr1:207664243
|
C | T | 3 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-13146C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207664243 | ||||||
| chr1:207664245
|
T | C | 193 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.98-13144T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207664245 | ||||||
| chr1:207664395
|
A | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-12994A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207664395 | ||||||
| chr1:207664539
|
G | A | 1 | a0002c0002t0001g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.98-12850G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207664539 | ||||||
| chr1:207664839
|
AAGATAAT others(11): Show |
A | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.98-12545_98-12528d others(20): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207664839 | |||||
| chr1:207664984
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.98-12405C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207664984 | ||||||
| chr1:207665007
|
T | G | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-12382T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665007 | ||||||
| chr1:207665051
|
G | A | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.98-12338G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665051 | ||||||
| chr1:207665074
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-12315G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665074 | ||||||
| chr1:207665084
|
T | C | 193 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.98-12305T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665084 | ||||||
| chr1:207665103
|
G | A | 1 | a0002c0002t0001g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.98-12286G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665103 | ||||||
| chr1:207665120
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-12269C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665120 | ||||||
| chr1:207665168
|
C | T | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.98-12221C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665168 | ||||||
| chr1:207665334
|
G | A | 4 | a0002c0002t0001g0054a0002c0002t0001g0076a0002c0002t0001g0077others(1): Show | 4 | HG00741.hp1 HG01175.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-12055G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665334 | ||||||
| chr1:207665372
|
A | C | 1 | a0015c0024t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.98-12017A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665372 | ||||||
| chr1:207665404
|
A | AT | 185 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 197 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.98-11976dupT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207665404 | |||||
| chr1:207665418
|
T | C | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-11971T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665418 | ||||||
| chr1:207665424
|
C | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-11965C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665424 | ||||||
| chr1:207665481
|
C | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-11908C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665481 | ||||||
| chr1:207665570
|
T | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-11819T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665570 | ||||||
| chr1:207665629
|
G | A | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-11760G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665629 | ||||||
| chr1:207665639
|
C | T | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-11750C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665639 | ||||||
| chr1:207665656
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.98-11733A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665656 | ||||||
| chr1:207665673
|
G | A | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-11716G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665673 | ||||||
| chr1:207665829
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.98-11560C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665829 | ||||||
| chr1:207665897
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.98-11492G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665897 | ||||||
| chr1:207665923
|
T | C | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-11466T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665923 | ||||||
| chr1:207665925
|
C | T | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-11464C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665925 | ||||||
| chr1:207665983
|
C | A | 4 | a0002c0002t0001g0078a0002c0002t0001g0079a0002c0002t0001g0080others(1): Show | 4 | HG00423.hp2 HG02135.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-11406C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207665983 | ||||||
| chr1:207666160
|
C | G | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.98-11229C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666160 | ||||||
| chr1:207666190
|
A | G | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-11199A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666190 | ||||||
| chr1:207666308
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-11081C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666308 | ||||||
| chr1:207666322
|
G | A | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-11067G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666322 | ||||||
| chr1:207666424
|
C | G | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-10965C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666424 | ||||||
| chr1:207666599
|
G | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-10790G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666599 | ||||||
| chr1:207666617
|
T | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-10772T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666617 | ||||||
| chr1:207666657
|
C | T | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-10732C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666657 | ||||||
| chr1:207666663
|
G | C | 1 | a0002c0002t0001g0103 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.98-10726G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666663 | ||||||
| chr1:207666707
|
A | G | 1 | a0004c0004t0001g0314 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.98-10682A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666707 | ||||||
| chr1:207666715
|
G | A | 1 | a0001c0001t0001g0008 | 2 | HG00438.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.98-10674G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666715 | ||||||
| chr1:207666926
|
G | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-10463G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207666926 | ||||||
| chr1:207667177
|
G | A | 1 | a0003c0003t0001g0184 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.98-10212G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207667177 | ||||||
| chr1:207667431
|
G | A | 128 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(125): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-9958G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207667431 | ||||||
| chr1:207667717
|
CAGAGTGA others(4745): Show |
C | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-9668_98-4917del | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207667717 | |||||
| chr1:207667726
|
G | GA | 4 | a0001c0001t0001g0009a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 5 | HG01515.hp1 HG01517.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-9656dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207667726 | |||||
| chr1:207667861
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0248a0001c0001t0001g0249others(6): Show | 10 | HG01192.hp2 HG02257.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.98-9528C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207667861 | ||||||
| chr1:207667869
|
G | A | 5 | a0001c0017t0001g0125a0001c0017t0001g0170a0007c0007t0001g0126others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-9520G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207667869 | ||||||
| chr1:207667904
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.98-9485G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207667904 | ||||||
| chr1:207668164
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.98-9225T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668164 | ||||||
| chr1:207668280
|
A | G | 1 | a0011c0015t0001g0016 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.98-9109A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668280 | ||||||
| chr1:207668379
|
A | T | 1 | a0009c0010t0001g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.98-9010A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668379 | ||||||
| chr1:207668400
|
A | T | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.98-8989A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668400 | ||||||
| chr1:207668556
|
G | A | 2 | a0001c0001t0001g0280a0007c0007t0001g0281 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.98-8833G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668556 | ||||||
| chr1:207668589
|
T | C | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-8800T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668589 | ||||||
| chr1:207668662
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-8727C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668662 | ||||||
| chr1:207668759
|
A | C | 70 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(67): Show | 72 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.98-8630A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668759 | ||||||
| chr1:207668874
|
A | G | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-8515A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668874 | ||||||
| chr1:207668875
|
T | C | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-8514T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207668875 | ||||||
| chr1:207669134
|
G | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-8255G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669134 | ||||||
| chr1:207669144
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-8245C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669144 | ||||||
| chr1:207669237
|
T | G | 4 | a0002c0002t0001g0081a0006c0006t0001g0056a0006c0006t0001g0060others(1): Show | 4 | HG00609.hp1 HG00673.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-8152T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669237 | ||||||
| chr1:207669359
|
T | C | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-8030T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669359 | ||||||
| chr1:207669393
|
TATTTCAG others(11): Show |
T | 121 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(118): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.98-7993_98-7976del others(18): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207669393 | |||||
| chr1:207669488
|
C | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-7901C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669488 | ||||||
| chr1:207669555
|
G | A | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(91): Show | 101 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.98-7834G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669555 | ||||||
| chr1:207669655
|
G | A | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-7734G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669655 | ||||||
| chr1:207669811
|
G | A | 1 | a0015c0024t0001g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.98-7578G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669811 | ||||||
| chr1:207669989
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.98-7400A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207669989 | ||||||
| chr1:207670036
|
T | C | 1 | a0029c0026t0001g0317 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.98-7353T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207670036 | ||||||
| chr1:207670558
|
T | C | 183 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0278others(180): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.98-6831T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207670558 | ||||||
| chr1:207670717
|
C | T | 121 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(118): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.98-6672C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207670717 | ||||||
| chr1:207670968
|
G | A | 2 | a0005c0005t0001g0029a0005c0005t0001g0030 | 2 | HG06807.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.98-6421G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207670968 | ||||||
| chr1:207671104
|
G | A | 1 | a0001c0017t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.98-6285G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671104 | ||||||
| chr1:207671140
|
G | A | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-6249G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671140 | ||||||
| chr1:207671274
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 5 | HG01515.hp1 HG01517.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-6115C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671274 | ||||||
| chr1:207671280
|
A | G | 121 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(118): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.98-6109A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671280 | ||||||
| chr1:207671454
|
T | C | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-5935T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671454 | ||||||
| chr1:207671455
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.98-5934C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671455 | ||||||
| chr1:207671643
|
G | A | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-5746G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671643 | ||||||
| chr1:207671665
|
A | G | 1 | a0003c0003t0001g0228 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.98-5724A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671665 | ||||||
| chr1:207671777
|
T | C | 125 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(122): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-5612T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671777 | ||||||
| chr1:207671821
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98-5568T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207671821 | ||||||
| chr1:207672286
|
G | A | 9 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-5103G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207672286 | ||||||
| chr1:207672430
|
T | C | 1 | a0004c0004t0001g0318 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.98-4959T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207672430 | ||||||
| chr1:207672605
|
C | T | 1 | a0003c0003t0001g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.98-4784C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207672605 | ||||||
| chr1:207672658
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98-4731A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207672658 | ||||||
| chr1:207672723
|
G | A | 3 | a0002c0002t0001g0105a0006c0006t0001g0064a0006c0006t0001g0104 | 3 | HG00140.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.98-4666G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207672723 | ||||||
| chr1:207672737
|
C | T | 1 | a0023c0033t0001g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98-4652C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207672737 | ||||||
| chr1:207672897
|
A | T | 121 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0282others(118): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.98-4492A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207672897 | ||||||
| chr1:207673067
|
G | T | 1 | a0003c0003t0001g0148 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.98-4322G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673067 | ||||||
| chr1:207673083
|
A | G | 1 | a0023c0033t0001g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98-4306A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673083 | ||||||
| chr1:207673182
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.98-4207G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673182 | ||||||
| chr1:207673256
|
G | A | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-4133G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673256 | ||||||
| chr1:207673317
|
T | TTA | 125 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(122): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.98-4068_98-4067dup others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207673317 | |||||
| chr1:207673485
|
G | A | 111 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(108): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.98-3904G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673485 | ||||||
| chr1:207673485
|
G | T | 5 | a0001c0017t0001g0125a0001c0017t0001g0170a0007c0007t0001g0126others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-3904G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673485 | ||||||
| chr1:207673526
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-3863C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673526 | ||||||
| chr1:207673638
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.98-3751T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673638 | ||||||
| chr1:207673678
|
A | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-3711A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673678 | ||||||
| chr1:207673717
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-3672G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673717 | ||||||
| chr1:207673769
|
ACC | A | 9 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-3619_98-3618del others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673769 | ||||||
| chr1:207673773
|
T | G | 9 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-3616T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673773 | ||||||
| chr1:207673783
|
C | T | 111 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(108): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.98-3606C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673783 | ||||||
| chr1:207673849
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.98-3540A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673849 | ||||||
| chr1:207673850
|
A | C | 125 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(122): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.98-3539A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673850 | ||||||
| chr1:207673884
|
G | T | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.98-3505G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673884 | ||||||
| chr1:207673979
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.98-3410C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207673979 | ||||||
| chr1:207674061
|
A | T | 1 | a0005c0005t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98-3328A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674061 | ||||||
| chr1:207674065
|
C | A | 125 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(122): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.98-3324C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674065 | ||||||
| chr1:207674076
|
A | G | 1 | a0018c0021t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-3313A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674076 | ||||||
| chr1:207674167
|
C | T | 1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.98-3222C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674167 | ||||||
| chr1:207674278
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.98-3111T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674278 | ||||||
| chr1:207674350
|
C | A | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-3039C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674350 | ||||||
| chr1:207674516
|
T | C | 2 | a0016c0016t0001g0124a0016c0016t0001g0166 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-2873T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674516 | ||||||
| chr1:207674531
|
C | T | 125 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(122): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.98-2858C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674531 | ||||||
| chr1:207674563
|
A | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-2826A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674563 | ||||||
| chr1:207674706
|
T | C | 125 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(122): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.98-2683T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674706 | ||||||
| chr1:207674722
|
G | A | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-2667G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674722 | ||||||
| chr1:207674788
|
T | C | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-2601T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674788 | ||||||
| chr1:207674793
|
T | C | 1 | a0005c0005t0001g0031 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.98-2596T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674793 | ||||||
| chr1:207674862
|
G | GT | 25 | a0002c0002t0001g0101a0005c0005t0001g0017a0005c0005t0001g0018others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.98-2526dupT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207674862 | |||||
| chr1:207674864
|
G | GTT | 9 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-2515_98-2514dup others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207674864 | |||||
| chr1:207674864
|
G | T | 111 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(108): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.98-2525G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207674864 | ||||||
| chr1:207675006
|
T | G | 9 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-2383T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207675006 | ||||||
| chr1:207675273
|
T | TATC | 111 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(108): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.98-2114_98-2113ins others(3): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207675273 | |||||
| chr1:207675353
|
G | A | 2 | a0005c0005t0001g0029a0005c0005t0001g0030 | 2 | HG06807.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.98-2036G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207675353 | ||||||
| chr1:207675358
|
G | C | 1 | a0005c0005t0001g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.98-2031G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207675358 | ||||||
| chr1:207675583
|
A | T | 1 | a0003c0003t0001g0221 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.98-1806A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207675583 | ||||||
| chr1:207675869
|
A | G | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.98-1520A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207675869 | ||||||
| chr1:207676260
|
A | T | 11 | a0001c0001t0001g0167a0002c0002t0001g0003a0002c0002t0001g0264others(8): Show | 13 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-1129A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676260 | ||||||
| chr1:207676299
|
T | C | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.98-1090T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676299 | ||||||
| chr1:207676470
|
C | T | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-919C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676470 | ||||||
| chr1:207676481
|
GGTTGCAT others(5): Show |
G | 1 | a0019c0022t0001g0265 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.98-907_98-896delGT others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676481 | ||||||
| chr1:207676494
|
C | A | 1 | a0019c0022t0001g0265 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.98-895C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676494 | ||||||
| chr1:207676571
|
T | G | 167 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(164): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.98-818T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676571 | ||||||
| chr1:207676592
|
C | T | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.98-797C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676592 | ||||||
| chr1:207676713
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.98-676G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676713 | ||||||
| chr1:207676844
|
C | T | 1 | a0007c0007t0001g0322 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.98-545C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676844 | ||||||
| chr1:207676902
|
C | A | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-487C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207676902 | ||||||
| chr1:207677179
|
G | A | 1 | a0005c0005t0001g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.98-210G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207677179 | ||||||
| chr1:207677194
|
C | T | 313 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(310): Show | 330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.98-195C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207677194 | ||||||
| chr1:207677215
|
A | G | 113 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.98-174A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207677215 | ||||||
| chr1:207677244
|
A | C | 113 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.98-145A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207677244 | ||||||
| chr1:207677307
|
C | CA | 21 | a0001c0001t0001g0139a0001c0001t0001g0208a0001c0001t0001g0249others(18): Show | 21 | HG00741.hp2 HG01109.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-52dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207677307 | |||||
| chr1:207677307
|
C | CAA | 10 | a0001c0001t0001g0134a0004c0004t0001g0014a0004c0004t0001g0286others(7): Show | 11 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-53_98-52dupAA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207677307 | |||||
| chr1:207677307
|
CA | C | 77 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(74): Show | 85 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.98-52delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207677307 | |||||
| chr1:207677307
|
CAAAA | C | 10 | a0001c0001t0001g0167a0001c0017t0001g0125a0002c0002t0001g0003others(7): Show | 12 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-55_98-52delAAAA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207677307 | |||||
| chr1:207677307
|
CAAAAA | C | 19 | a0002c0002t0001g0043a0002c0002t0001g0044a0002c0002t0001g0045others(16): Show | 19 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.98-56_98-52delAAAA others(1): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207677307 | |||||
| chr1:207677307
|
CAAAAAA | C | 88 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(85): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.98-57_98-52delAAAA others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207677307 | |||||
| chr1:207677307
|
CAAAAAAA | C | 9 | a0002c0002t0001g0115a0002c0002t0001g0175a0002c0002t0001g0176others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-58_98-52delAAAA others(3): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 207677307 | |||||
| chr1:207677321
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.98-68A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207677321 | ||||||
| chr1:207677372
|
G | A | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-17G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 1/11 | chr1 | 207677372 | ||||||
| chr1:207677593
|
C | A | 1 | a0004c0004t0001g0272 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.277+25C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | chr1 | 207677593 | ||||||
| chr1:207677593
|
C | T | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+25C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | chr1 | 207677593 | ||||||
| chr1:207677619
|
T | C | 1 | a0005c0005t0001g0024 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.277+51T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | chr1 | 207677619 | ||||||
| chr1:207677715
|
C | T | 1 | a0014c0023t0001g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.277+147C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | chr1 | 207677715 | ||||||
| chr1:207677824
|
T | C | 113 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.277+256T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | chr1 | 207677824 | ||||||
| chr1:207677910
|
C | T | 167 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(164): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.278-288C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | chr1 | 207677910 | ||||||
| chr1:207677958
|
G | A | 1 | a0002c0002t0001g0083 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.278-240G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | chr1 | 207677958 | ||||||
| chr1:207678016
|
C | T | 113 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.278-182C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | chr1 | 207678016 | ||||||
| chr1:207678142
|
T | TA | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.278-47dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 207678142 | |||||
| chr1:207678348
|
C | A | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.377+51C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678348 | ||||||
| chr1:207678415
|
G | A | 113 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.377+118G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678415 | ||||||
| chr1:207678461
|
G | T | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.377+164G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678461 | ||||||
| chr1:207678635
|
A | G | 1 | a0004c0004t0001g0271 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.377+338A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678635 | ||||||
| chr1:207678673
|
A | G | 14 | a0002c0002t0001g0059a0002c0002t0001g0065a0002c0002t0001g0081others(11): Show | 14 | HG00609.hp1 HG00673.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.377+376A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678673 | ||||||
| chr1:207678776
|
G | C | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.377+479G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678776 | ||||||
| chr1:207678815
|
C | T | 1 | a0015c0024t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.377+518C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678815 | ||||||
| chr1:207678881
|
G | A | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.377+584G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678881 | ||||||
| chr1:207678928
|
C | T | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.377+631C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207678928 | ||||||
| chr1:207678996
|
CT | C | 70 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0202others(67): Show | 74 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.377+717delT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207678996 | |||||
| chr1:207678996
|
CTTT | C | 102 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(99): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.377+715_377+717del others(3): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207678996 | |||||
| chr1:207678996
|
CTTTT | C | 10 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(7): Show | 10 | HG01109.hp1 HG01167.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.377+714_377+717del others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207678996 | |||||
| chr1:207679073
|
T | G | 1 | a0028c0028t0001g0189 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.377+776T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679073 | ||||||
| chr1:207679153
|
A | AT | 119 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0155others(116): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.377+879dupT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207679153 | |||||
| chr1:207679153
|
A | ATT | 14 | a0002c0002t0001g0045a0002c0002t0001g0051a0002c0002t0001g0052others(11): Show | 14 | HG01081.hp2 HG01261.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.377+878_377+879dup others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207679153 | |||||
| chr1:207679153
|
AT | A | 8 | a0001c0013t0001g0011a0003c0003t0001g0240a0004c0004t0001g0289others(5): Show | 9 | HG00099.hp2 HG01257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.377+879delT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207679153 | |||||
| chr1:207679153
|
ATT | A | 10 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.377+878_377+879del others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207679153 | |||||
| chr1:207679225
|
G | C | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377+928G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679225 | ||||||
| chr1:207679246
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.377+949G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679246 | ||||||
| chr1:207679255
|
C | A | 184 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0017t0001g0125others(181): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.377+958C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679255 | ||||||
| chr1:207679267
|
A | G | 1 | a0004c0004t0001g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.377+970A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679267 | ||||||
| chr1:207679297
|
A | G | 167 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(164): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.377+1000A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679297 | ||||||
| chr1:207679322
|
A | G | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.377+1025A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679322 | ||||||
| chr1:207679348
|
G | C | 113 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.377+1051G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679348 | ||||||
| chr1:207679397
|
G | A | 10 | a0002c0002t0001g0057a0002c0002t0001g0075a0002c0002t0001g0084others(7): Show | 10 | HG01978.hp1 NA18941.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.377+1100G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679397 | ||||||
| chr1:207679635
|
A | T | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.377+1338A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207679635 | ||||||
| chr1:207680354
|
C | T | 2 | a0004c0004t0001g0298a0004c0004t0001g0305 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.377+2057C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680354 | ||||||
| chr1:207680453
|
T | C | 1 | a0002c0002t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.377+2156T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680453 | ||||||
| chr1:207680537
|
TA | T | 63 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(60): Show | 65 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.377+2247delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207680537 | |||||
| chr1:207680541
|
A | AT | 72 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(69): Show | 77 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.377+2244_377+2245i others(3): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680541 | ||||||
| chr1:207680542
|
A | T | 106 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(103): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.377+2245A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680542 | ||||||
| chr1:207680543
|
A | T | 176 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(173): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.377+2246A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680543 | ||||||
| chr1:207680544
|
A | T | 183 | a0001c0001t0001g0171a0001c0017t0001g0125a0001c0017t0001g0170others(180): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.377+2247A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680544 | ||||||
| chr1:207680545
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.377+2248T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680545 | ||||||
| chr1:207680579
|
C | G | 176 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(173): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.377+2282C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680579 | ||||||
| chr1:207680690
|
T | C | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.377+2393T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680690 | ||||||
| chr1:207680801
|
G | A | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.377+2504G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680801 | ||||||
| chr1:207680963
|
C | A | 1 | a0003c0003t0001g0148 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.377+2666C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207680963 | ||||||
| chr1:207681010
|
G | T | 115 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.377+2713G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681010 | ||||||
| chr1:207681064
|
G | A | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.377+2767G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681064 | ||||||
| chr1:207681128
|
C | T | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.378-2744C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681128 | ||||||
| chr1:207681139
|
G | T | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.378-2733G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681139 | ||||||
| chr1:207681207
|
T | C | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.378-2665T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681207 | ||||||
| chr1:207681293
|
T | A | 176 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(173): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.378-2579T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681293 | ||||||
| chr1:207681327
|
C | T | 106 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(103): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.378-2545C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681327 | ||||||
| chr1:207681358
|
G | A | 176 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(173): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.378-2514G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681358 | ||||||
| chr1:207681401
|
A | G | 1 | a0003c0003t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.378-2471A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681401 | ||||||
| chr1:207681414
|
C | A | 9 | a0003c0003t0001g0006a0003c0003t0001g0116a0003c0003t0001g0122others(6): Show | 10 | HG01256.hp1 HG01928.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-2458C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681414 | ||||||
| chr1:207681435
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.378-2437G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681435 | ||||||
| chr1:207681482
|
A | T | 115 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.378-2390A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681482 | ||||||
| chr1:207681574
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-2298G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681574 | ||||||
| chr1:207681688
|
T | C | 2 | a0016c0016t0001g0124a0016c0016t0001g0166 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.378-2184T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681688 | ||||||
| chr1:207681738
|
C | T | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-2134C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681738 | ||||||
| chr1:207681750
|
C | T | 115 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.378-2122C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681750 | ||||||
| chr1:207681862
|
T | C | 1 | a0003c0003t0001g0007 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.378-2010T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207681862 | ||||||
| chr1:207682015
|
C | T | 1 | a0004c0004t0001g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.378-1857C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682015 | ||||||
| chr1:207682053
|
G | A | 4 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110others(1): Show | 4 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-1819G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682053 | ||||||
| chr1:207682074
|
G | A | 10 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(7): Show | 10 | HG01109.hp1 HG01433.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1798G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682074 | ||||||
| chr1:207682210
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0250a0001c0001t0001g0251others(1): Show | 5 | HG01192.hp2 HG02300.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.378-1662C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682210 | ||||||
| chr1:207682220
|
C | A | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.378-1652C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682220 | ||||||
| chr1:207682246
|
GA | G | 176 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(173): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.378-1623delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682246 | |||||
| chr1:207682318
|
A | C | 1 | a0001c0001t0001g0155 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.378-1554A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682318 | ||||||
| chr1:207682455
|
A | C | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.378-1417A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682455 | ||||||
| chr1:207682482
|
A | G | 1 | a0002c0002t0001g0052 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.378-1390A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682482 | ||||||
| chr1:207682664
|
A | G | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.378-1208A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682664 | ||||||
| chr1:207682695
|
G | A | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.378-1177G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682695 | ||||||
| chr1:207682960
|
T | TTTCTTTC others(28): Show |
1 | a0001c0017t0001g0125 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.378-910_378-909ins others(35): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682960
|
T | TTTTC | 11 | a0001c0001t0001g0185a0001c0001t0001g0232a0001c0001t0001g0278others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.378-884_378-881dup others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682960
|
T | TTTTCTTT others(5): Show |
2 | a0018c0021t0001g0268a0022c0032t0001g0270 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.378-892_378-881dup others(12): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682960
|
T | TTTTCTTT others(9): Show |
3 | a0001c0001t0001g0167a0001c0001t0001g0171a0009c0010t0001g0328 | 3 | HG01109.hp2 HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.378-896_378-881dup others(16): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682960
|
T | TTTTCTTT others(17): Show |
3 | a0001c0017t0001g0170a0008c0027t0001g0169a0018c0021t0001g0266 | 3 | HG02630.hp1 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.378-904_378-881dup others(24): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682960
|
T | TTTTCTTT others(21): Show |
3 | a0007c0007t0001g0126a0007c0007t0001g0168a0025c0030t0001g0118 | 3 | HG02055.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.378-908_378-881dup others(28): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682960
|
T | TTTTCTTT others(29): Show |
1 | a0023c0033t0001g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.378-881_378-880ins others(36): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682960
|
T | TTTTCTTT others(33): Show |
1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.378-881_378-880ins others(40): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682960
|
TTTTCTTT others(1): Show |
T | 69 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(66): Show | 71 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.378-888_378-881del others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682960 | |||||
| chr1:207682972
|
C | CTTTCTTT others(5): Show |
12 | a0002c0002t0001g0003a0002c0002t0001g0115a0002c0002t0001g0127others(9): Show | 14 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.378-889_378-888ins others(12): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682972 | |||||
| chr1:207682976
|
C | CTTTCTTT others(1): Show |
30 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0021others(27): Show | 33 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.378-889_378-888ins others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682976 | |||||
| chr1:207682984
|
C | T | 1 | a0005c0005t0001g0019 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.378-888C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682984 | ||||||
| chr1:207682988
|
C | CT | 10 | a0001c0001t0001g0211a0001c0001t0001g0236a0001c0001t0001g0250others(7): Show | 10 | HG00408.hp2 HG00735.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-877dupT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682988 | |||||
| chr1:207682992
|
T | C | 86 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(83): Show | 91 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.378-880T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682992 | ||||||
| chr1:207682996
|
C | CTTTCTTT others(11): Show |
4 | a0004c0004t0001g0274a0004c0004t0001g0320a0004c0004t0001g0321others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-865_378-864ins others(18): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207682996 | |||||
| chr1:207682996
|
C | T | 34 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(31): Show | 37 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.378-876C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207682996 | ||||||
| chr1:207683010
|
T | TTCTTTCT others(37): Show |
1 | a0004c0004t0001g0318 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.378-861_378-860ins others(44): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTCT others(33): Show |
1 | a0004c0004t0001g0291 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.378-861_378-860ins others(40): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTCT others(25): Show |
2 | a0015c0024t0001g0260a0015c0024t0001g0262 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.378-861_378-860ins others(32): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTCT others(23): Show |
1 | a0004c0004t0001g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.378-861_378-860ins others(30): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTCT others(21): Show |
1 | a0014c0023t0001g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.378-861_378-860ins others(28): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTCT others(25): Show |
10 | a0004c0004t0001g0284a0004c0004t0001g0286a0004c0004t0001g0296others(7): Show | 10 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-861_378-860ins others(32): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTCT others(21): Show |
12 | a0004c0004t0001g0014a0004c0004t0001g0114a0004c0004t0001g0292others(9): Show | 13 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.378-861_378-860ins others(28): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTTT others(13): Show |
1 | a0014c0023t0001g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.378-861_378-860ins others(20): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTTT others(17): Show |
11 | a0004c0004t0001g0013a0004c0004t0001g0272a0004c0004t0001g0273others(8): Show | 12 | HG00609.hp2 HG02040.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.378-861_378-860ins others(24): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
T | TTCTTTTT others(18): Show |
1 | a0004c0004t0001g0311 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.378-861_378-860ins others(25): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683010
|
TTTTC | T | 71 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(68): Show | 73 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.378-849_378-846del others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683010 | |||||
| chr1:207683012
|
T | C | 38 | a0004c0004t0001g0274a0004c0004t0001g0320a0004c0004t0001g0321others(35): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.378-860T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683012 | ||||||
| chr1:207683014
|
C | CTT | 37 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(34): Show | 39 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.378-856_378-855dup others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683014 | |||||
| chr1:207683014
|
C | CTTTTTTT others(15): Show |
8 | a0004c0004t0001g0271a0004c0004t0001g0288a0004c0004t0001g0289others(5): Show | 8 | HG00673.hp1 NA18960.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.378-855_378-854ins others(22): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683014 | |||||
| chr1:207683014
|
C | T | 38 | a0004c0004t0001g0274a0004c0004t0001g0320a0004c0004t0001g0321others(35): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.378-858C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683014 | ||||||
| chr1:207683016
|
T | TTC | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-854_378-853dup others(2): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 207683016 | |||||
| chr1:207683027
|
C | T | 1 | a0026c0031t0001g0263 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.378-845C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683027 | ||||||
| chr1:207683105
|
T | C | 5 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0191others(2): Show | 5 | NA18964.hp1 NA18965.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.378-767T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683105 | ||||||
| chr1:207683139
|
G | A | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.378-733G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683139 | ||||||
| chr1:207683207
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.378-665A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683207 | ||||||
| chr1:207683313
|
T | A | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.378-559T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683313 | ||||||
| chr1:207683321
|
G | T | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.378-551G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683321 | ||||||
| chr1:207683442
|
A | T | 169 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(166): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.378-430A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683442 | ||||||
| chr1:207683450
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.378-422C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683450 | ||||||
| chr1:207683523
|
A | G | 115 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.378-349A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683523 | ||||||
| chr1:207683774
|
T | C | 1 | a0004c0004t0001g0318 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.378-98T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683774 | ||||||
| chr1:207683813
|
T | C | 103 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(100): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.378-59T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 3/11 | chr1 | 207683813 | ||||||
| chr1:207684051
|
T | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+94T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684051 | ||||||
| chr1:207684143
|
G | A | 2 | a0022c0032t0001g0270a0023c0033t0001g0269 | 2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.463+186G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684143 | ||||||
| chr1:207684380
|
T | G | 1 | a0001c0001t0001g0278 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+423T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684380 | ||||||
| chr1:207684415
|
C | T | 115 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.463+458C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684415 | ||||||
| chr1:207684428
|
A | G | 115 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.463+471A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684428 | ||||||
| chr1:207684467
|
G | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+510G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684467 | ||||||
| chr1:207684684
|
T | C | 2 | a0001c0001t0001g0156a0003c0003t0001g0150 | 2 | HG03688.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.463+727T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684684 | ||||||
| chr1:207684772
|
T | TA | 13 | a0002c0002t0001g0004a0002c0002t0001g0044a0002c0002t0001g0045others(10): Show | 14 | HG00558.hp1 HG00738.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.463+824dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207684772 | |||||
| chr1:207684772
|
TA | T | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.463+824delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207684772 | |||||
| chr1:207684828
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+871G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684828 | ||||||
| chr1:207684862
|
A | C | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.463+905A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684862 | ||||||
| chr1:207684946
|
A | G | 2 | a0001c0001t0001g0280a0007c0007t0001g0281 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.463+989A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684946 | ||||||
| chr1:207684957
|
A | T | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.463+1000A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684957 | ||||||
| chr1:207684984
|
A | G | 1 | a0002c0002t0001g0065 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.463+1027A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207684984 | ||||||
| chr1:207685169
|
A | G | 1 | a0003c0003t0001g0164 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.463+1212A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685169 | ||||||
| chr1:207685182
|
G | C | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.463+1225G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685182 | ||||||
| chr1:207685200
|
A | G | 7 | a0006c0006t0001g0327a0018c0021t0001g0266a0018c0021t0001g0268others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.463+1243A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685200 | ||||||
| chr1:207685201
|
T | C | 115 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.463+1244T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685201 | ||||||
| chr1:207685241
|
G | A | 106 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(103): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.463+1284G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685241 | ||||||
| chr1:207685248
|
G | A | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+1291G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685248 | ||||||
| chr1:207685249
|
A | G | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+1292A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685249 | ||||||
| chr1:207685273
|
C | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463+1316C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685273 | ||||||
| chr1:207685276
|
C | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463+1319C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685276 | ||||||
| chr1:207685316
|
C | A | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.463+1359C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685316 | ||||||
| chr1:207685469
|
C | G | 54 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(51): Show | 56 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.463+1512C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685469 | ||||||
| chr1:207685591
|
G | A | 1 | a0005c0005t0001g0035 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.463+1634G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685591 | ||||||
| chr1:207685701
|
G | C | 1 | a0002c0002t0001g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.463+1744G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685701 | ||||||
| chr1:207685729
|
G | A | 1 | a0002c0002t0001g0113 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.463+1772G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685729 | ||||||
| chr1:207685793
|
T | G | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+1836T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685793 | ||||||
| chr1:207685832
|
G | C | 1 | a0004c0004t0001g0014 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.463+1875G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685832 | ||||||
| chr1:207685851
|
C | T | 7 | a0006c0006t0001g0327a0018c0021t0001g0266a0018c0021t0001g0268others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.463+1894C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685851 | ||||||
| chr1:207685903
|
A | G | 2 | a0022c0032t0001g0270a0023c0033t0001g0269 | 2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.463+1946A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685903 | ||||||
| chr1:207685906
|
G | A | 277 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(274): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.463+1949G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685906 | ||||||
| chr1:207685917
|
G | C | 327 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(324): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.463+1960G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685917 | ||||||
| chr1:207685985
|
T | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2028T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207685985 | ||||||
| chr1:207686075
|
T | C | 115 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.463+2118T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686075 | ||||||
| chr1:207686076
|
C | CTCCCTCC others(5): Show |
7 | a0005c0005t0001g0018a0005c0005t0001g0020a0005c0005t0001g0021others(4): Show | 7 | HG00323.hp1 HG01167.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.463+2128_463+2129i others(14): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686076 | |||||
| chr1:207686082
|
C | CCCTCCAT others(9): Show |
1 | a0005c0005t0001g0025 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.463+2128_463+2129i others(18): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686082 | |||||
| chr1:207686082
|
CCCTTCCT others(17): Show |
C | 3 | a0014c0023t0001g0261a0015c0024t0001g0260a0015c0024t0001g0262 | 3 | HG03704.hp2 HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.463+2129_463+2152d others(26): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686082 | |||||
| chr1:207686086
|
T | C | 164 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(161): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.463+2129T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686086 | ||||||
| chr1:207686088
|
C | A | 104 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(101): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.463+2131C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686088 | ||||||
| chr1:207686094
|
CCTTT | C | 48 | a0002c0002t0001g0042a0002c0002t0001g0043a0002c0002t0001g0047others(45): Show | 51 | HG00558.hp1 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.463+2139_463+2142d others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686094 | |||||
| chr1:207686094
|
CCTTTCCT others(1): Show |
C | 12 | a0002c0002t0001g0005a0002c0002t0001g0072a0002c0002t0001g0083others(9): Show | 13 | HG01074.hp2 HG01099.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.463+2139_463+2146d others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686094 | |||||
| chr1:207686096
|
T | C | 61 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0070others(58): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.463+2139T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686096 | ||||||
| chr1:207686098
|
T | C | 7 | a0005c0005t0001g0018a0005c0005t0001g0020a0005c0005t0001g0021others(4): Show | 7 | HG00323.hp1 HG01167.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.463+2141T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686098 | ||||||
| chr1:207686102
|
T | C | 44 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0070others(41): Show | 47 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.463+2145T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686102 | ||||||
| chr1:207686106
|
T | C | 92 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0042others(89): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.463+2149T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686106 | ||||||
| chr1:207686106
|
T | TCCTCCCT others(253): Show |
1 | a0001c0001t0001g0137 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(262): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686106 | |||||
| chr1:207686108
|
C | CTCCCTCC others(249): Show |
3 | a0001c0001t0001g0212a0013c0011t0001g0140a0013c0011t0001g0145 | 3 | NA18963.hp2 NA18989.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(258): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686108 | |||||
| chr1:207686108
|
C | CTCCCTCC others(249): Show |
4 | a0001c0001t0001g0136a0001c0001t0001g0141a0001c0001t0001g0201others(1): Show | 4 | NA18944.hp2 NA18946.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(258): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686108 | |||||
| chr1:207686110
|
C | T | 9 | a0002c0002t0001g0267a0005c0005t0001g0018a0005c0005t0001g0020others(6): Show | 9 | HG00323.hp1 HG01167.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.463+2153C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686110 | ||||||
| chr1:207686112
|
C | A | 3 | a0014c0023t0001g0261a0015c0024t0001g0260a0015c0024t0001g0262 | 3 | HG03704.hp2 HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.463+2155C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686112 | ||||||
| chr1:207686114
|
C | CCCTCCCT others(253): Show |
1 | a0001c0001t0001g0149 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(262): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686114 | |||||
| chr1:207686114
|
C | CCCTCCCT others(253): Show |
16 | a0001c0001t0001g0139a0001c0001t0001g0144a0001c0001t0001g0193others(13): Show | 18 | HG01256.hp1 HG01261.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(262): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686114 | |||||
| chr1:207686114
|
C | T | 50 | a0002c0002t0001g0004a0002c0002t0001g0070a0002c0002t0001g0074others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.463+2157C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686114 | ||||||
| chr1:207686114
|
CCCTCCCT others(5): Show |
C | 2 | a0006c0006t0001g0104a0014c0023t0001g0257 | 2 | HG01099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.463+2173_463+2184d others(14): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686114 | |||||
| chr1:207686116
|
C | CTCCATCC others(85): Show |
4 | a0018c0021t0001g0266a0018c0021t0001g0268a0019c0022t0001g0265others(1): Show | 4 | HG02257.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2162_463+2163i others(94): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCATCC others(137): Show |
1 | a0022c0032t0001g0270 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.463+2162_463+2163i others(146): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCATCC others(137): Show |
1 | a0023c0033t0001g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.463+2162_463+2163i others(146): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCATCC others(201): Show |
1 | a0007c0007t0001g0130 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.463+2162_463+2163i others(210): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(241): Show |
1 | a0003c0003t0001g0148 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(245): Show |
4 | a0001c0001t0001g0231a0001c0001t0001g0255a0008c0012t0001g0179others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(254): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(269): Show |
1 | a0001c0001t0001g0236 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(278): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(246): Show |
1 | a0003c0003t0001g0182 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(255): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(237): Show |
1 | a0003c0003t0001g0216 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(246): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(249): Show |
1 | a0008c0027t0001g0169 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(258): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(241): Show |
1 | a0001c0017t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(245): Show |
1 | a0003c0008t0001g0225 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(254): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(245): Show |
1 | a0001c0001t0001g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(254): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(241): Show |
3 | a0003c0008t0001g0142a0003c0008t0001g0194a0003c0008t0001g0196 | 3 | NA18960.hp2 NA18977.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(241): Show |
1 | a0003c0003t0001g0162 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(241): Show |
36 | a0001c0001t0001g0008a0001c0001t0001g0146a0001c0001t0001g0152others(33): Show | 40 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(409): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0251 | 3 | HG01192.hp2 HG02300.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(418): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(409): Show |
4 | a0001c0001t0001g0248a0001c0001t0001g0252a0001c0001t0001g0258others(1): Show | 4 | HG02615.hp2 HG03831.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(418): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(233): Show |
2 | a0001c0001t0001g0134a0007c0007t0001g0119 | 2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(242): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(225): Show |
3 | a0001c0001t0001g0238a0001c0001t0001g0245a0003c0008t0001g0188 | 3 | HG02523.hp1 NA18988.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(234): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(237): Show |
1 | a0028c0028t0001g0189 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(246): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(241): Show |
3 | a0003c0003t0001g0239a0003c0003t0001g0242a0003c0003t0001g0243 | 3 | HG01070.hp1 HG03491.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686116
|
C | CTCCCTCC others(133): Show |
1 | a0004c0004t0001g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(142): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686116 | |||||
| chr1:207686118
|
C | CCCTCCCT others(249): Show |
5 | a0001c0001t0001g0143a0001c0001t0001g0191a0001c0001t0001g0202others(2): Show | 5 | HG02293.hp1 NA18954.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(258): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686118 | |||||
| chr1:207686118
|
C | CCCTCCCT others(249): Show |
1 | a0001c0001t0001g0200 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(258): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686118 | |||||
| chr1:207686118
|
C | T | 97 | a0002c0002t0001g0004a0002c0002t0001g0042a0002c0002t0001g0043others(94): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.463+2161C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686118 | ||||||
| chr1:207686120
|
C | A | 2 | a0006c0006t0001g0327a0007c0007t0001g0129 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.463+2163C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686120 | ||||||
| chr1:207686120
|
C | CTCCCTCC others(241): Show |
1 | a0008c0012t0001g0235 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686120 | |||||
| chr1:207686120
|
C | CTCCCTCC others(237): Show |
1 | a0001c0001t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(246): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686120 | |||||
| chr1:207686120
|
C | CTCCCTCC others(237): Show |
2 | a0003c0003t0001g0177a0007c0007t0001g0168 | 2 | HG00741.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(246): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686120 | |||||
| chr1:207686120
|
C | CTCCCTCC others(361): Show |
1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(370): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686120 | |||||
| chr1:207686122
|
C | CCCTCCCT others(249): Show |
2 | a0001c0001t0001g0280a0007c0007t0001g0281 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(258): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(245): Show |
1 | a0001c0001t0001g0009 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(254): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(245): Show |
22 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0154others(19): Show | 23 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(254): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(261): Show |
1 | a0003c0003t0001g0190 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(270): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(265): Show |
1 | a0003c0003t0001g0206 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(274): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(249): Show |
1 | a0003c0003t0001g0161 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(258): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(413): Show |
1 | a0001c0001t0001g0249 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.463+2168_463+2169i others(422): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(237): Show |
2 | a0007c0007t0001g0131a0007c0007t0001g0178 | 2 | HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(246): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(237): Show |
1 | a0009c0010t0001g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(246): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(381): Show |
1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(390): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(249): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0222 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(258): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(241): Show |
2 | a0001c0001t0001g0185a0001c0001t0001g0187 | 2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | CCCTCCCT others(109): Show |
1 | a0004c0004t0001g0310 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(118): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686122 | |||||
| chr1:207686122
|
C | T | 113 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(110): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.463+2165C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686122 | ||||||
| chr1:207686124
|
C | CTCCCTTC others(241): Show |
6 | a0001c0001t0001g0278a0007c0007t0001g0275a0007c0007t0001g0276others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(250): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686124 | |||||
| chr1:207686124
|
C | CTCCCTTC others(233): Show |
1 | a0007c0007t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.463+2168_463+2169i others(242): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686124 | |||||
| chr1:207686124
|
C | CTCCCTTC others(401): Show |
2 | a0001c0001t0001g0250a0001c0001t0001g0256 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.463+2168_463+2169i others(410): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686124 | |||||
| chr1:207686124
|
C | CTCCCTTC others(121): Show |
3 | a0004c0004t0001g0014a0004c0004t0001g0295a0004c0004t0001g0296 | 4 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(130): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686124 | |||||
| chr1:207686124
|
C | CTCCCTTC others(125): Show |
44 | a0004c0004t0001g0013a0004c0004t0001g0114a0004c0004t0001g0271others(41): Show | 45 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.463+2168_463+2169i others(134): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686124 | |||||
| chr1:207686126
|
T | C | 117 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0136others(114): Show | 121 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.463+2169T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686126 | ||||||
| chr1:207686126
|
T | TCCTTCCT others(233): Show |
2 | a0009c0010t0001g0120a0009c0010t0001g0133 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.463+2172_463+2173i others(242): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686126 | |||||
| chr1:207686126
|
T | TCCTTCCT others(245): Show |
1 | a0003c0003t0001g0230 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.463+2172_463+2173i others(254): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686126 | |||||
| chr1:207686128
|
C | CTTCCTTC others(229): Show |
1 | a0001c0001t0001g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.463+2172_463+2173i others(238): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686128 | |||||
| chr1:207686130
|
C | T | 142 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0139others(139): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.463+2173C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686130 | ||||||
| chr1:207686134
|
C | CCCTCCCT others(329): Show |
1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+2180_463+2181i others(338): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686134 | |||||
| chr1:207686134
|
C | CCCTCCCT others(209): Show |
1 | a0007c0007t0001g0129 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.463+2180_463+2181i others(218): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686134 | |||||
| chr1:207686134
|
C | CCCTTCCT others(1): Show |
39 | a0001c0001t0001g0008a0001c0001t0001g0138a0001c0001t0001g0146others(36): Show | 42 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.463+2216_463+2223d others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686134 | |||||
| chr1:207686134
|
C | T | 236 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0136others(233): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.463+2177C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686134 | ||||||
| chr1:207686138
|
T | C | 69 | a0001c0001t0001g0232a0001c0001t0001g0250a0001c0001t0001g0256others(66): Show | 71 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.463+2181T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686138 | ||||||
| chr1:207686142
|
T | C | 58 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0256others(55): Show | 60 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.463+2185T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686142 | ||||||
| chr1:207686142
|
T | TCCTCCCT others(1): Show |
6 | a0018c0021t0001g0266a0018c0021t0001g0268a0019c0022t0001g0265others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+2188_463+2189i others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686142 | |||||
| chr1:207686142
|
T | TCCTTCCT others(111): Show |
1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2196_463+2197i others(120): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686142 | |||||
| chr1:207686146
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.463+2189T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686146 | ||||||
| chr1:207686149
|
T | C | 1 | a0005c0005t0001g0025 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.463+2192T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686149 | ||||||
| chr1:207686149
|
T | TTCCTTCC others(1): Show |
4 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110others(1): Show | 4 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+2199_463+2200i others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686149 | |||||
| chr1:207686157
|
T | C | 12 | a0005c0005t0001g0018a0005c0005t0001g0020a0005c0005t0001g0021others(9): Show | 12 | HG00323.hp1 HG00735.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.463+2200T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686157 | ||||||
| chr1:207686157
|
T | TTCCTTCC others(1): Show |
14 | a0005c0005t0001g0017a0005c0005t0001g0019a0005c0005t0001g0022others(11): Show | 14 | HG00099.hp1 HG00408.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.463+2207_463+2208i others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686157 | |||||
| chr1:207686165
|
T | C | 98 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(95): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.463+2208T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686165 | ||||||
| chr1:207686165
|
T | TTCCC | 4 | a0002c0002t0001g0079a0002c0002t0001g0080a0005c0005t0001g0028others(1): Show | 4 | HG00423.hp2 HG01192.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2211_463+2212i others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686165 | |||||
| chr1:207686173
|
T | C | 168 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(165): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.463+2216T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686173 | ||||||
| chr1:207686173
|
T | TTCCC | 4 | a0002c0002t0001g0127a0002c0002t0001g0175a0016c0016t0001g0166others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2219_463+2220i others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207686173 | |||||
| chr1:207686181
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0256 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.463+2224C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686181 | ||||||
| chr1:207686232
|
C | A | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2275C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686232 | ||||||
| chr1:207686233
|
A | C | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2276A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686233 | ||||||
| chr1:207686234
|
C | A | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2277C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686234 | ||||||
| chr1:207686254
|
T | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2297T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686254 | ||||||
| chr1:207686323
|
A | C | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2366A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686323 | ||||||
| chr1:207686324
|
C | A | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2367C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686324 | ||||||
| chr1:207686354
|
G | C | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.463+2397G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686354 | ||||||
| chr1:207686398
|
T | C | 118 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0005others(115): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.463+2441T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686398 | ||||||
| chr1:207686448
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.463+2491C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686448 | ||||||
| chr1:207686603
|
T | A | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2646T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686603 | ||||||
| chr1:207686604
|
A | T | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2647A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686604 | ||||||
| chr1:207686605
|
T | A | 1 | a0004c0004t0001g0326 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.463+2648T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686605 | ||||||
| chr1:207686719
|
A | T | 9 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0172others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.463+2762A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686719 | ||||||
| chr1:207686796
|
G | A | 4 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110others(1): Show | 4 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+2839G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686796 | ||||||
| chr1:207686813
|
C | G | 50 | a0004c0004t0001g0013a0004c0004t0001g0014a0004c0004t0001g0114others(47): Show | 52 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.463+2856C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686813 | ||||||
| chr1:207686901
|
C | T | 8 | a0006c0006t0001g0327a0018c0021t0001g0266a0018c0021t0001g0268others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.463+2944C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686901 | ||||||
| chr1:207686940
|
G | C | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+2983G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207686940 | ||||||
| chr1:207687016
|
T | C | 1 | a0018c0021t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.463+3059T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687016 | ||||||
| chr1:207687066
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.463+3109G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687066 | ||||||
| chr1:207687197
|
T | C | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.463+3240T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687197 | ||||||
| chr1:207687264
|
A | G | 2 | a0021c0018t0001g0205a0021c0018t0001g0217 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.463+3307A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687264 | ||||||
| chr1:207687283
|
G | A | 3 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267 | 5 | HG01891.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+3326G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687283 | ||||||
| chr1:207687321
|
T | C | 3 | a0003c0003t0001g0007a0003c0003t0001g0240a0003c0003t0001g0246 | 4 | HG00099.hp2 HG01099.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+3364T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687321 | ||||||
| chr1:207687453
|
C | G | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+3496C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687453 | ||||||
| chr1:207687462
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.463+3505T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687462 | ||||||
| chr1:207687719
|
C | A | 2 | a0007c0007t0001g0129a0007c0007t0001g0130 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.463+3762C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687719 | ||||||
| chr1:207687807
|
T | C | 1 | a0004c0004t0001g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.463+3850T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687807 | ||||||
| chr1:207687862
|
A | G | 99 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0042others(96): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.463+3905A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687862 | ||||||
| chr1:207687914
|
G | A | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.463+3957G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207687914 | ||||||
| chr1:207688011
|
G | A | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.463+4054G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688011 | ||||||
| chr1:207688347
|
T | C | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463+4390T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688347 | ||||||
| chr1:207688353
|
T | G | 2 | a0012c0014t0001g0096a0012c0014t0001g0097 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.463+4396T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688353 | ||||||
| chr1:207688379
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+4422C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688379 | ||||||
| chr1:207688440
|
CA | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+4491delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207688440 | |||||
| chr1:207688527
|
A | G | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+4570A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688527 | ||||||
| chr1:207688581
|
A | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0256 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.463+4624A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688581 | ||||||
| chr1:207688604
|
TTCCACAA others(6): Show |
T | 1 | a0003c0003t0001g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.463+4651_463+4663d others(15): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207688604 | |||||
| chr1:207688649
|
A | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+4692A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688649 | ||||||
| chr1:207688659
|
T | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+4702T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688659 | ||||||
| chr1:207688831
|
T | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+4874T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688831 | ||||||
| chr1:207688949
|
A | T | 3 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267 | 5 | HG01891.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+4992A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207688949 | ||||||
| chr1:207689014
|
T | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+5057T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689014 | ||||||
| chr1:207689128
|
T | A | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+5171T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689128 | ||||||
| chr1:207689183
|
A | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5170A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689183 | ||||||
| chr1:207689281
|
A | C | 1 | a0022c0032t0001g0270 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.464-5072A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689281 | ||||||
| chr1:207689345
|
A | G | 2 | a0012c0014t0001g0096a0012c0014t0001g0097 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.464-5008A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689345 | ||||||
| chr1:207689353
|
T | A | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.464-5000T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689353 | ||||||
| chr1:207689373
|
G | T | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-4980G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689373 | ||||||
| chr1:207689417
|
CGTT | C | 4 | a0002c0002t0001g0054a0002c0002t0001g0076a0002c0002t0001g0077others(1): Show | 4 | HG00741.hp1 HG01175.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-4933_464-4931d others(5): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207689417 | |||||
| chr1:207689448
|
G | A | 1 | a0004c0004t0001g0303 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.464-4905G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689448 | ||||||
| chr1:207689530
|
A | G | 1 | a0002c0002t0001g0050 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.464-4823A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689530 | ||||||
| chr1:207689549
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.464-4804A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689549 | ||||||
| chr1:207689682
|
T | C | 2 | a0001c0001t0001g0193a0003c0003t0001g0192 | 2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.464-4671T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689682 | ||||||
| chr1:207689764
|
G | A | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.464-4589G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689764 | ||||||
| chr1:207689906
|
A | G | 1 | a0002c0002t0001g0072 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.464-4447A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207689906 | ||||||
| chr1:207690088
|
A | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4265A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690088 | ||||||
| chr1:207690247
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 9 | HG00438.hp1 NA18954.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-4106A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690247 | ||||||
| chr1:207690401
|
T | A | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-3952T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690401 | ||||||
| chr1:207690493
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.464-3860G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690493 | ||||||
| chr1:207690718
|
T | A | 7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0236others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-3635T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690718 | ||||||
| chr1:207690822
|
G | A | 1 | a0003c0003t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.464-3531G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690822 | ||||||
| chr1:207690829
|
G | A | 1 | a0003c0003t0001g0206 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.464-3524G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690829 | ||||||
| chr1:207690882
|
T | G | 1 | a0003c0003t0001g0182 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.464-3471T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690882 | ||||||
| chr1:207690887
|
T | C | 4 | a0004c0004t0001g0287a0004c0004t0001g0288a0004c0004t0001g0289others(1): Show | 4 | NA18960.hp1 NA18962.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-3466T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207690887 | ||||||
| chr1:207691118
|
A | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-3235A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207691118 | ||||||
| chr1:207691153
|
A | T | 3 | a0001c0001t0001g0212a0013c0011t0001g0140a0013c0011t0001g0145 | 3 | NA18963.hp2 NA18989.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.464-3200A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207691153 | ||||||
| chr1:207691324
|
A | T | 1 | a0022c0032t0001g0270 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.464-3029A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207691324 | ||||||
| chr1:207691408
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.464-2945G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207691408 | ||||||
| chr1:207691805
|
A | G | 3 | a0006c0006t0001g0056a0006c0006t0001g0060a0006c0006t0001g0082 | 3 | HG00609.hp1 NA18945.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.464-2548A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207691805 | ||||||
| chr1:207691816
|
A | T | 2 | a0003c0003t0001g0229a0003c0003t0001g0230 | 2 | HG00323.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.464-2537A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207691816 | ||||||
| chr1:207691897
|
G | C | 1 | a0004c0004t0001g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.464-2456G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207691897 | ||||||
| chr1:207691999
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-2354G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207691999 | ||||||
| chr1:207692065
|
A | G | 1 | a0003c0003t0001g0184 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.464-2288A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692065 | ||||||
| chr1:207692087
|
C | T | 1 | a0002c0002t0001g0071 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.464-2266C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692087 | ||||||
| chr1:207692229
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.464-2124T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692229 | ||||||
| chr1:207692421
|
G | T | 1 | a0002c0002t0001g0050 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.464-1932G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692421 | ||||||
| chr1:207692447
|
T | C | 5 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(2): Show | 5 | NA18747.hp2 NA18947.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-1906T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692447 | ||||||
| chr1:207692479
|
C | T | 9 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-1874C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692479 | ||||||
| chr1:207692513
|
G | A | 2 | a0009c0010t0001g0328a0031c0025t0001g0062 | 2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.464-1840G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692513 | ||||||
| chr1:207692520
|
C | A | 5 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(2): Show | 5 | NA18747.hp2 NA18947.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-1833C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692520 | ||||||
| chr1:207692526
|
G | A | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.464-1827G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692526 | ||||||
| chr1:207692548
|
T | A | 5 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(2): Show | 5 | NA18747.hp2 NA18947.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-1805T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692548 | ||||||
| chr1:207692581
|
T | C | 9 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | NA18747.hp2 NA18947.hp2 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-1772T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692581 | ||||||
| chr1:207692596
|
T | C | 1 | a0006c0006t0001g0099 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.464-1757T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692596 | ||||||
| chr1:207692704
|
C | T | 9 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-1649C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692704 | ||||||
| chr1:207692710
|
A | G | 9 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-1643A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692710 | ||||||
| chr1:207692728
|
C | G | 9 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-1625C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692728 | ||||||
| chr1:207692730
|
CTACGT | C | 9 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-1621_464-1617d others(7): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 207692730 | |||||
| chr1:207692743
|
A | G | 9 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-1610A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692743 | ||||||
| chr1:207692757
|
T | G | 9 | a0002c0002t0001g0059a0002c0002t0001g0098a0002c0002t0001g0100others(6): Show | 9 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-1596T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692757 | ||||||
| chr1:207692765
|
T | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-1588T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692765 | ||||||
| chr1:207692798
|
A | C | 2 | a0009c0010t0001g0328a0031c0025t0001g0062 | 2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.464-1555A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692798 | ||||||
| chr1:207692807
|
T | G | 94 | a0001c0001t0001g0171a0002c0002t0001g0005a0002c0002t0001g0042others(91): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.464-1546T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207692807 | ||||||
| chr1:207693779
|
G | A | 1 | a0019c0022t0001g0265 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.464-574G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207693779 | ||||||
| chr1:207693831
|
G | A | 152 | a0001c0001t0001g0198a0002c0002t0001g0005a0002c0002t0001g0042others(149): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.464-522G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207693831 | ||||||
| chr1:207693853
|
T | C | 2 | a0009c0010t0001g0328a0031c0025t0001g0062 | 2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.464-500T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207693853 | ||||||
| chr1:207693943
|
A | C | 1 | a0029c0026t0001g0317 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.464-410A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207693943 | ||||||
| chr1:207693955
|
T | A | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-398T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207693955 | ||||||
| chr1:207693956
|
C | T | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-397C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207693956 | ||||||
| chr1:207693962
|
C | T | 1 | a0005c0005t0001g0023 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.464-391C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207693962 | ||||||
| chr1:207694054
|
A | C | 1 | a0002c0002t0001g0049 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.464-299A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207694054 | ||||||
| chr1:207694159
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19063.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.464-194T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207694159 | ||||||
| chr1:207694162
|
T | C | 1 | a0004c0004t0001g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.464-191T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207694162 | ||||||
| chr1:207694241
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.464-112C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207694241 | ||||||
| chr1:207694301
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-52G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207694301 | ||||||
| chr1:207694319
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.464-34A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 4/11 | chr1 | 207694319 | ||||||
| chr1:207694787
|
T | G | 1 | a0015c0024t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.862+36T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207694787 | ||||||
| chr1:207694860
|
A | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+109A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207694860 | ||||||
| chr1:207695208
|
C | T | 7 | a0018c0021t0001g0266a0018c0021t0001g0268a0019c0022t0001g0174others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.862+457C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695208 | ||||||
| chr1:207695249
|
C | T | 58 | a0002c0002t0001g0005a0002c0002t0001g0042a0002c0002t0001g0043others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.862+498C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695249 | ||||||
| chr1:207695265
|
A | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+514A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695265 | ||||||
| chr1:207695283
|
A | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+532A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695283 | ||||||
| chr1:207695302
|
A | T | 1 | a0018c0021t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.862+551A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695302 | ||||||
| chr1:207695449
|
A | C | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.862+698A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695449 | ||||||
| chr1:207695467
|
G | A | 2 | a0022c0032t0001g0270a0023c0033t0001g0269 | 2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.862+716G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695467 | ||||||
| chr1:207695495
|
G | A | 1 | a0002c0002t0001g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.862+744G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695495 | ||||||
| chr1:207695510
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+759C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695510 | ||||||
| chr1:207695627
|
C | G | 85 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(82): Show | 89 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.862+876C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695627 | ||||||
| chr1:207695780
|
A | T | 2 | a0006c0006t0001g0327a0025c0030t0001g0118 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.862+1029A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695780 | ||||||
| chr1:207695857
|
A | C | 1 | a0003c0003t0001g0180 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.862+1106A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695857 | ||||||
| chr1:207695929
|
C | T | 2 | a0001c0001t0001g0280a0007c0007t0001g0281 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.862+1178C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695929 | ||||||
| chr1:207695936
|
C | A | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.862+1185C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695936 | ||||||
| chr1:207695964
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.862+1213G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207695964 | ||||||
| chr1:207696100
|
G | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+1349G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696100 | ||||||
| chr1:207696135
|
G | C | 1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.863-1368G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696135 | ||||||
| chr1:207696231
|
G | C | 1 | a0002c0002t0001g0084 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.863-1272G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696231 | ||||||
| chr1:207696387
|
A | C | 15 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267others(12): Show | 17 | HG01109.hp2 HG01891.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.863-1116A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696387 | ||||||
| chr1:207696486
|
A | G | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.863-1017A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696486 | ||||||
| chr1:207696550
|
A | C | 4 | a0001c0001t0001g0171a0001c0017t0001g0125a0001c0017t0001g0170others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.863-953A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696550 | ||||||
| chr1:207696628
|
T | A | 1 | a0012c0014t0001g0093 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.863-875T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696628 | ||||||
| chr1:207696783
|
C | T | 1 | a0004c0004t0001g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.863-720C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696783 | ||||||
| chr1:207696784
|
G | A | 1 | a0003c0003t0001g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.863-719G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696784 | ||||||
| chr1:207696810
|
C | T | 3 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267 | 5 | HG01891.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.863-693C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696810 | ||||||
| chr1:207696885
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.863-618C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696885 | ||||||
| chr1:207696951
|
G | A | 1 | a0004c0004t0001g0304 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.863-552G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207696951 | ||||||
| chr1:207697120
|
G | T | 164 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0198others(161): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.863-383G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207697120 | ||||||
| chr1:207697337
|
A | C | 51 | a0001c0001t0001g0198a0004c0004t0001g0013a0004c0004t0001g0014others(48): Show | 53 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.863-166A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207697337 | ||||||
| chr1:207697349
|
C | T | 1 | a0009c0010t0001g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.863-154C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 5/11 | chr1 | 207697349 | ||||||
| chr1:207697704
|
G | A | 1 | a0004c0004t0001g0304 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1039+25G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 6/11 | chr1 | 207697704 | ||||||
| chr1:207697921
|
G | A | 1 | a0006c0006t0001g0082 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1142+48G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207697921 | ||||||
| chr1:207697971
|
G | C | 2 | a0022c0032t0001g0270a0023c0033t0001g0269 | 2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1142+98G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207697971 | ||||||
| chr1:207697975
|
G | C | 28 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1142+102G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207697975 | ||||||
| chr1:207697975
|
G | GAC | 9 | a0001c0001t0001g0012a0001c0001t0001g0278a0002c0002t0001g0003others(6): Show | 12 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1142+122_1142+123d others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 207697975 | |||||
| chr1:207697975
|
G | GACACAC | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1142+118_1142+123d others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 207697975 | |||||
| chr1:207698062
|
C | T | 4 | a0005c0005t0001g0034a0005c0005t0001g0035a0005c0005t0001g0039others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1142+189C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207698062 | ||||||
| chr1:207698484
|
A | G | 164 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0198others(161): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1142+611A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207698484 | ||||||
| chr1:207698579
|
C | A | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1143-610C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207698579 | ||||||
| chr1:207698664
|
CTTCTT | C | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-523_1143-519d others(7): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 207698664 | |||||
| chr1:207698945
|
T | C | 28 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1143-244T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207698945 | ||||||
| chr1:207699011
|
C | T | 4 | a0001c0001t0001g0171a0001c0017t0001g0125a0001c0017t0001g0170others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143-178C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207699011 | ||||||
| chr1:207699162
|
G | A | 66 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(63): Show | 70 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1143-27G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 7/11 | chr1 | 207699162 | ||||||
| chr1:207699312
|
C | T | 28 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228+38C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699312 | ||||||
| chr1:207699338
|
T | C | 5 | a0018c0021t0001g0266a0018c0021t0001g0268a0019c0022t0001g0174others(2): Show | 5 | HG02257.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228+64T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699338 | ||||||
| chr1:207699382
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1228+108T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699382 | ||||||
| chr1:207699490
|
A | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0138a0001c0001t0001g0151others(59): Show | 66 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1228+216A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699490 | ||||||
| chr1:207699516
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0116a0003c0003t0001g0121others(10): Show | 14 | HG01175.hp2 HG01256.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1228+242C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699516 | ||||||
| chr1:207699559
|
T | C | 2 | a0006c0006t0001g0327a0025c0030t0001g0118 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1228+285T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699559 | ||||||
| chr1:207699850
|
A | G | 94 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(91): Show | 98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1228+576A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699850 | ||||||
| chr1:207699901
|
A | G | 1 | a0005c0005t0001g0023 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1228+627A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699901 | ||||||
| chr1:207699969
|
A | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267 | 5 | HG01891.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228+695A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207699969 | ||||||
| chr1:207700002
|
T | G | 2 | a0019c0022t0001g0174a0026c0031t0001g0263 | 2 | HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1228+728T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700002 | ||||||
| chr1:207700041
|
T | G | 3 | a0019c0022t0001g0174a0019c0022t0001g0265a0026c0031t0001g0263 | 3 | HG02257.hp1 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1228+767T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700041 | ||||||
| chr1:207700044
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0248a0001c0001t0001g0249others(9): Show | 13 | HG01192.hp2 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228+770G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700044 | ||||||
| chr1:207700051
|
A | G | 2 | a0004c0004t0001g0287a0004c0004t0001g0290 | 2 | NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1228+777A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700051 | ||||||
| chr1:207700059
|
TA | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228+787delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 207700059 | |||||
| chr1:207700218
|
T | G | 10 | a0001c0001t0001g0134a0007c0007t0001g0119a0007c0007t0001g0129others(7): Show | 10 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1228+944T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700218 | ||||||
| chr1:207700423
|
G | A | 9 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0236others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1229-1096G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700423 | ||||||
| chr1:207700548
|
C | G | 2 | a0009c0010t0001g0328a0031c0025t0001g0062 | 2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1229-971C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700548 | ||||||
| chr1:207700556
|
C | G | 28 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1229-963C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700556 | ||||||
| chr1:207700626
|
A | G | 1 | a0022c0032t0001g0270 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1229-893A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700626 | ||||||
| chr1:207700656
|
G | A | 2 | a0006c0006t0001g0327a0025c0030t0001g0118 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1229-863G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700656 | ||||||
| chr1:207700722
|
CAT | C | 51 | a0001c0001t0001g0198a0004c0004t0001g0013a0004c0004t0001g0014others(48): Show | 53 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1229-791_1229-790d others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 207700722 | |||||
| chr1:207700736
|
A | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1229-783A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700736 | ||||||
| chr1:207700761
|
C | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1229-758C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700761 | ||||||
| chr1:207700827
|
G | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1229-692G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700827 | ||||||
| chr1:207700831
|
G | T | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1229-688G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700831 | ||||||
| chr1:207700927
|
C | T | 90 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(87): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1229-592C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700927 | ||||||
| chr1:207700981
|
A | G | 12 | a0001c0001t0001g0134a0001c0001t0001g0250a0001c0001t0001g0256others(9): Show | 12 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1229-538A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207700981 | ||||||
| chr1:207701163
|
G | A | 90 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(87): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1229-356G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701163 | ||||||
| chr1:207701285
|
T | C | 6 | a0002c0002t0001g0005a0002c0002t0001g0042a0002c0002t0001g0043others(3): Show | 7 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1229-234T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701285 | ||||||
| chr1:207701289
|
C | G | 3 | a0001c0017t0001g0125a0001c0017t0001g0170a0008c0027t0001g0169 | 3 | HG02630.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1229-230C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701289 | ||||||
| chr1:207701295
|
T | C | 2 | a0009c0010t0001g0120a0009c0010t0001g0133 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1229-224T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701295 | ||||||
| chr1:207701359
|
G | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(102): Show | 113 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1229-160G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701359 | ||||||
| chr1:207701365
|
G | C | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1229-154G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701365 | ||||||
| chr1:207701370
|
T | G | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1229-149T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701370 | ||||||
| chr1:207701394
|
C | G | 94 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(91): Show | 98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1229-125C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701394 | ||||||
| chr1:207701409
|
C | A | 2 | a0004c0004t0001g0274a0004c0004t0001g0320 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1229-110C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701409 | ||||||
| chr1:207701413
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1229-106C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701413 | ||||||
| chr1:207701417
|
A | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0264a0002c0002t0001g0267 | 5 | HG01891.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1229-102A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701417 | ||||||
| chr1:207701444
|
T | G | 1 | a0004c0004t0001g0308 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1229-75T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 8/11 | chr1 | 207701444 | ||||||
| chr1:207701771
|
GAGA | G | 51 | a0001c0001t0001g0198a0004c0004t0001g0013a0004c0004t0001g0014others(48): Show | 53 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1328+157_1328+159d others(5): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207701771 | |||||
| chr1:207701830
|
G | T | 121 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(118): Show | 129 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1328+212G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207701830 | ||||||
| chr1:207701899
|
C | G | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1328+281C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207701899 | ||||||
| chr1:207702086
|
A | G | 93 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(90): Show | 97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1328+468A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702086 | ||||||
| chr1:207702124
|
G | A | 1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1328+506G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702124 | ||||||
| chr1:207702178
|
G | T | 94 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(91): Show | 98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1328+560G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702178 | ||||||
| chr1:207702192
|
T | C | 3 | a0003c0003t0001g0180a0003c0003t0001g0181a0003c0003t0001g0247 | 3 | HG00735.hp1 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1328+574T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702192 | ||||||
| chr1:207702216
|
T | A | 58 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(55): Show | 62 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1328+598T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702216 | ||||||
| chr1:207702524
|
C | A | 3 | a0003c0003t0001g0158a0003c0003t0001g0159a0003c0003t0001g0160 | 3 | NA18959.hp1 NA19066.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1328+906C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702524 | ||||||
| chr1:207702604
|
A | C | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1328+986A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702604 | ||||||
| chr1:207702632
|
G | A | 51 | a0001c0001t0001g0198a0004c0004t0001g0013a0004c0004t0001g0014others(48): Show | 53 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1328+1014G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702632 | ||||||
| chr1:207702723
|
C | T | 8 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(5): Show | 8 | HG00099.hp1 HG01106.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1328+1105C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702723 | ||||||
| chr1:207702836
|
A | T | 58 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(55): Show | 62 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1328+1218A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702836 | ||||||
| chr1:207702851
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1328+1233G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702851 | ||||||
| chr1:207702952
|
G | A | 4 | a0014c0023t0001g0257a0014c0023t0001g0261a0015c0024t0001g0260others(1): Show | 4 | HG01981.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1328+1334G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702952 | ||||||
| chr1:207702976
|
C | T | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1328+1358C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207702976 | ||||||
| chr1:207703205
|
A | G | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0141others(1): Show | 4 | NA18946.hp1 NA18952.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1328+1587A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207703205 | ||||||
| chr1:207703232
|
C | A | 51 | a0001c0001t0001g0198a0004c0004t0001g0013a0004c0004t0001g0014others(48): Show | 53 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1328+1614C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207703232 | ||||||
| chr1:207703335
|
A | G | 1 | a0004c0004t0001g0294 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1328+1717A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207703335 | ||||||
| chr1:207703740
|
A | G | 1 | a0018c0021t0001g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1328+2122A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207703740 | ||||||
| chr1:207703757
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1328+2139C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207703757 | ||||||
| chr1:207703916
|
C | T | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1328+2298C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207703916 | ||||||
| chr1:207703917
|
G | A | 58 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(55): Show | 62 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1328+2299G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207703917 | ||||||
| chr1:207703956
|
A | AAAAAAG | 57 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(54): Show | 61 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1328+2349_1328+235 others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207703956 | |||||
| chr1:207703980
|
A | G | 1 | a0004c0004t0001g0271 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1328+2362A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207703980 | ||||||
| chr1:207704070
|
G | T | 26 | a0005c0005t0001g0017a0005c0005t0001g0018a0005c0005t0001g0019others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1328+2452G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207704070 | ||||||
| chr1:207704096
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1328+2478G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207704096 | ||||||
| chr1:207704164
|
C | T | 59 | a0001c0001t0001g0198a0002c0002t0001g0005a0002c0002t0001g0042others(56): Show | 60 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1328+2546C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207704164 | ||||||
| chr1:207704345
|
GTAGATTT others(1): Show |
G | 8 | a0002c0002t0001g0004a0002c0002t0001g0047a0002c0002t0001g0048others(5): Show | 9 | HG00558.hp1 HG00738.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1328+2729_1328+273 others(12): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207704345 | |||||
| chr1:207704354
|
T | A | 8 | a0002c0002t0001g0004a0002c0002t0001g0047a0002c0002t0001g0048others(5): Show | 9 | HG00558.hp1 HG00738.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1328+2736T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207704354 | ||||||
| chr1:207704552
|
T | A | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1328+2934T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207704552 | ||||||
| chr1:207704851
|
T | G | 1 | a0006c0006t0001g0104 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1328+3233T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207704851 | ||||||
| chr1:207704927
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1329-3251T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207704927 | ||||||
| chr1:207705296
|
G | A | 57 | a0001c0001t0001g0198a0002c0002t0001g0003a0002c0002t0001g0264others(54): Show | 61 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1329-2882G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705296 | ||||||
| chr1:207705309
|
G | C | 1 | a0001c0001t0001g0252 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1329-2869G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705309 | ||||||
| chr1:207705359
|
C | T | 1 | a0023c0033t0001g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329-2819C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705359 | ||||||
| chr1:207705372
|
C | A | 1 | a0012c0014t0001g0093 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1329-2806C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705372 | ||||||
| chr1:207705442
|
A | G | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329-2736A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705442 | ||||||
| chr1:207705469
|
A | G | 2 | a0012c0014t0001g0096a0012c0014t0001g0097 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1329-2709A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705469 | ||||||
| chr1:207705476
|
A | G | 1 | a0026c0031t0001g0263 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1329-2702A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705476 | ||||||
| chr1:207705524
|
C | T | 5 | a0004c0004t0001g0321a0014c0023t0001g0257a0014c0023t0001g0261others(2): Show | 5 | HG01981.hp1 HG03225.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1329-2654C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705524 | ||||||
| chr1:207705765
|
C | G | 2 | a0019c0022t0001g0174a0019c0022t0001g0265 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1329-2413C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705765 | ||||||
| chr1:207705768
|
A | G | 2 | a0019c0022t0001g0174a0019c0022t0001g0265 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1329-2410A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705768 | ||||||
| chr1:207705956
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1329-2222G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207705956 | ||||||
| chr1:207706013
|
G | GTA | 12 | a0002c0002t0001g0094a0002c0002t0001g0105a0002c0002t0001g0127others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.1329-2134_1329-213 others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
G | GTATATA | 9 | a0004c0004t0001g0014a0005c0005t0001g0017a0005c0005t0001g0018others(6): Show | 10 | HG00280.hp1 HG00423.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1329-2138_1329-213 others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
G | GTATATAT others(1): Show |
3 | a0002c0002t0001g0087a0005c0005t0001g0019a0005c0005t0001g0027 | 3 | HG01358.hp1 HG01433.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1329-2140_1329-213 others(12): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
G | GTATATAT others(3): Show |
6 | a0001c0001t0001g0223a0002c0002t0001g0045a0005c0005t0001g0022others(3): Show | 6 | HG01081.hp1 HG03831.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1329-2142_1329-213 others(14): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
G | GTATATAT others(5): Show |
1 | a0005c0005t0001g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1329-2144_1329-213 others(16): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
G | GTATATAT others(7): Show |
1 | a0005c0005t0001g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1329-2146_1329-213 others(18): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
G | GTATATAT others(9): Show |
2 | a0005c0005t0001g0024a0005c0005t0001g0031 | 2 | HG00099.hp1 HG00408.hp1 |
intron_variant | MODIFIER | c.1329-2148_1329-213 others(20): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
GTA | G | 82 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(79): Show | 84 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1329-2134_1329-213 others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
GTATA | G | 53 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0191others(50): Show | 54 | HG00280.hp2 HG00597.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1329-2136_1329-213 others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
GTATATA | G | 120 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(117): Show | 128 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1329-2138_1329-213 others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706013
|
GTATATAT others(1): Show |
G | 16 | a0001c0001t0001g0134a0001c0001t0001g0171a0001c0001t0001g0231others(13): Show | 16 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1329-2140_1329-213 others(12): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207706013 | |||||
| chr1:207706017
|
A | G | 14 | a0002c0002t0001g0057a0002c0002t0001g0075a0002c0002t0001g0084others(11): Show | 14 | HG01978.hp1 HG01981.hp1 HG03704.hp2 others(11): Show |
intron_variant | MODIFIER | c.1329-2161A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706017 | ||||||
| chr1:207706021
|
A | G | 2 | a0001c0001t0001g0167a0031c0025t0001g0062 | 2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1329-2157A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706021 | ||||||
| chr1:207706038
|
T | C | 159 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(156): Show | 167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1329-2140T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706038 | ||||||
| chr1:207706044
|
T | A | 12 | a0002c0002t0001g0071a0002c0002t0001g0075a0006c0006t0001g0058others(9): Show | 12 | HG01978.hp1 HG01981.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1329-2134T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706044 | ||||||
| chr1:207706113
|
A | G | 2 | a0001c0001t0001g0167a0018c0021t0001g0268 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1329-2065A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706113 | ||||||
| chr1:207706281
|
C | T | 70 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0167others(67): Show | 73 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1329-1897C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706281 | ||||||
| chr1:207706288
|
G | A | 7 | a0001c0001t0001g0236a0002c0002t0001g0115a0002c0002t0001g0127others(4): Show | 10 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1329-1890G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706288 | ||||||
| chr1:207706702
|
G | A | 1 | a0010c0009t0001g0001 | 4 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329-1476G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706702 | ||||||
| chr1:207706767
|
G | A | 46 | a0003c0003t0001g0006a0003c0003t0001g0116a0003c0003t0001g0117others(43): Show | 47 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1329-1411G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706767 | ||||||
| chr1:207706809
|
C | G | 182 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(179): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1329-1369C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706809 | ||||||
| chr1:207706835
|
A | G | 1 | a0014c0023t0001g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1329-1343A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706835 | ||||||
| chr1:207706889
|
T | A | 47 | a0003c0003t0001g0006a0003c0003t0001g0116a0003c0003t0001g0117others(44): Show | 48 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1329-1289T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706889 | ||||||
| chr1:207706946
|
G | C | 1 | a0002c0002t0001g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1329-1232G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706946 | ||||||
| chr1:207706983
|
A | G | 47 | a0003c0003t0001g0006a0003c0003t0001g0116a0003c0003t0001g0117others(44): Show | 48 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1329-1195A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207706983 | ||||||
| chr1:207707220
|
T | C | 10 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1329-958T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707220 | ||||||
| chr1:207707338
|
T | G | 248 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(245): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1329-840T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707338 | ||||||
| chr1:207707443
|
A | C | 245 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(242): Show | 259 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1329-735A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707443 | ||||||
| chr1:207707575
|
C | T | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1329-603C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707575 | ||||||
| chr1:207707632
|
A | C | 24 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0193others(21): Show | 25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1329-546A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707632 | ||||||
| chr1:207707671
|
T | A | 7 | a0004c0004t0001g0286a0004c0004t0001g0292a0004c0004t0001g0295others(4): Show | 7 | HG00280.hp2 HG01167.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329-507T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707671 | ||||||
| chr1:207707676
|
A | G | 2 | a0001c0001t0001g0278a0032c0038t0001g0173 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1329-502A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707676 | ||||||
| chr1:207707691
|
A | C | 244 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(241): Show | 258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1329-487A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707691 | ||||||
| chr1:207707785
|
T | TAC | 47 | a0001c0001t0001g0134a0002c0002t0001g0066a0002c0002t0001g0074others(44): Show | 48 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1329-359_1329-358d others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACAC | 19 | a0001c0001t0001g0171a0001c0001t0001g0231a0001c0001t0001g0236others(16): Show | 21 | HG01069.hp2 HG01109.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.1329-361_1329-358d others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACAC | 23 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0232others(20): Show | 25 | HG00558.hp1 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1329-363_1329-358d others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(1): Show |
19 | a0001c0001t0001g0010a0001c0001t0001g0139a0001c0001t0001g0146others(16): Show | 20 | HG00423.hp2 HG00597.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1329-365_1329-358d others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(3): Show |
77 | a0001c0001t0001g0008a0001c0001t0001g0151a0001c0001t0001g0152others(74): Show | 79 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1329-367_1329-358d others(12): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(5): Show |
53 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0137others(50): Show | 57 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1329-369_1329-358d others(14): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(7): Show |
24 | a0001c0001t0001g0167a0001c0001t0001g0201a0001c0001t0001g0207others(21): Show | 24 | HG01070.hp2 HG01071.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1329-371_1329-358d others(16): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(9): Show |
9 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(6): Show | 9 | HG02258.hp2 HG02965.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1329-373_1329-358d others(18): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(11): Show |
7 | a0002c0002t0001g0065a0002c0002t0001g0081a0004c0004t0001g0287others(4): Show | 7 | HG00099.hp1 HG00673.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329-375_1329-358d others(20): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(13): Show |
1 | a0005c0005t0001g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1329-377_1329-358d others(22): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(15): Show |
2 | a0005c0005t0001g0019a0005c0005t0001g0038 | 2 | HG01433.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1329-379_1329-358d others(24): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
T | TACACACA others(17): Show |
1 | a0005c0005t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1329-381_1329-358d others(26): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707785
|
TAC | T | 6 | a0006c0006t0001g0108a0006c0006t0001g0109a0006c0006t0001g0110others(3): Show | 6 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1329-359_1329-358d others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707785 | |||||
| chr1:207707813
|
CACACACA others(1): Show |
C | 7 | a0009c0010t0001g0120a0009c0010t0001g0132a0009c0010t0001g0133others(4): Show | 10 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1329-363_1329-356d others(10): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 207707813 | |||||
| chr1:207707821
|
T | C | 226 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(223): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1329-357T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707821 | ||||||
| chr1:207707835
|
G | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0258others(1): Show | 4 | HG02257.hp2 HG02615.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329-343G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707835 | ||||||
| chr1:207707894
|
A | G | 1 | a0002c0002t0001g0264 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1329-284A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707894 | ||||||
| chr1:207707911
|
G | A | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1329-267G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707911 | ||||||
| chr1:207707945
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1329-233A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707945 | ||||||
| chr1:207707966
|
G | A | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1329-212G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207707966 | ||||||
| chr1:207708002
|
T | C | 1 | a0022c0032t0001g0270 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1329-176T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207708002 | ||||||
| chr1:207708107
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1329-71C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207708107 | ||||||
| chr1:207708113
|
A | G | 11 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1329-65A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207708113 | ||||||
| chr1:207708140
|
TA | T | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1329-37delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207708140 | ||||||
| chr1:207708144
|
T | G | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1329-34T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207708144 | ||||||
| chr1:207708146
|
C | A | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1329-32C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207708146 | ||||||
| chr1:207708153
|
A | T | 1 | a0002c0002t0001g0101 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1329-25A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 9/11 | chr1 | 207708153 | ||||||
| chr1:207708274
|
A | T | 1 | a0018c0021t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1414+11A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708274 | ||||||
| chr1:207708296
|
C | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0258others(1): Show | 4 | HG02257.hp2 HG02615.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414+33C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708296 | ||||||
| chr1:207708311
|
G | A | 2 | a0007c0007t0001g0126a0007c0007t0001g0168 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1414+48G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708311 | ||||||
| chr1:207708480
|
T | C | 2 | a0007c0007t0001g0126a0007c0007t0001g0168 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1414+217T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708480 | ||||||
| chr1:207708509
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1414+246A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708509 | ||||||
| chr1:207708677
|
A | C | 7 | a0009c0010t0001g0120a0009c0010t0001g0132a0009c0010t0001g0133others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414+414A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708677 | ||||||
| chr1:207708838
|
T | G | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1414+575T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708838 | ||||||
| chr1:207708839
|
C | T | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1414+576C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708839 | ||||||
| chr1:207708846
|
G | C | 1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1414+583G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708846 | ||||||
| chr1:207708849
|
A | G | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1414+586A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708849 | ||||||
| chr1:207708877
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1414+614G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708877 | ||||||
| chr1:207708952
|
G | C | 28 | a0001c0001t0001g0134a0001c0001t0001g0167a0001c0001t0001g0171others(25): Show | 33 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1414+689G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207708952 | ||||||
| chr1:207709021
|
A | G | 2 | a0001c0001t0001g0232a0018c0021t0001g0268 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1414+758A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709021 | ||||||
| chr1:207709026
|
G | A | 1 | a0003c0003t0001g0122 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1414+763G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709026 | ||||||
| chr1:207709056
|
T | C | 296 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(293): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1414+793T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709056 | ||||||
| chr1:207709202
|
G | A | 7 | a0004c0004t0001g0286a0004c0004t0001g0292a0004c0004t0001g0295others(4): Show | 7 | HG00280.hp2 HG01167.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1414+939G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709202 | ||||||
| chr1:207709247
|
T | G | 234 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(231): Show | 248 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1414+984T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709247 | ||||||
| chr1:207709260
|
TG | T | 7 | a0009c0010t0001g0120a0009c0010t0001g0132a0009c0010t0001g0133others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414+1000delG | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207709260 | |||||
| chr1:207709294
|
T | C | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0258others(1): Show | 4 | HG02257.hp2 HG02615.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414+1031T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709294 | ||||||
| chr1:207709423
|
G | C | 1 | a0003c0003t0001g0241 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1414+1160G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709423 | ||||||
| chr1:207709522
|
A | G | 7 | a0009c0010t0001g0120a0009c0010t0001g0132a0009c0010t0001g0133others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414+1259A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709522 | ||||||
| chr1:207709596
|
G | A | 11 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1414+1333G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709596 | ||||||
| chr1:207709644
|
C | T | 1 | a0003c0003t0001g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1414+1381C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709644 | ||||||
| chr1:207709734
|
GGCT | G | 11 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1414+1474_1414+147 others(7): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207709734 | |||||
| chr1:207709795
|
A | G | 2 | a0007c0007t0001g0126a0007c0007t0001g0168 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1414+1532A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709795 | ||||||
| chr1:207709832
|
C | CA | 184 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(181): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1414+1584dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207709832 | |||||
| chr1:207709832
|
C | CAA | 48 | a0001c0001t0001g0134a0001c0001t0001g0155a0001c0001t0001g0167others(45): Show | 53 | HG00423.hp1 HG00597.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.1414+1583_1414+158 others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207709832 | |||||
| chr1:207709922
|
A | G | 19 | a0001c0001t0001g0134a0001c0001t0001g0171a0001c0001t0001g0231others(16): Show | 24 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1414+1659A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207709922 | ||||||
| chr1:207710028
|
C | G | 1 | a0018c0021t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1414+1765C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710028 | ||||||
| chr1:207710215
|
G | A | 2 | a0002c0002t0001g0073a0004c0004t0001g0321 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1414+1952G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710215 | ||||||
| chr1:207710234
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1414+1971C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710234 | ||||||
| chr1:207710248
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1414+1985G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710248 | ||||||
| chr1:207710298
|
G | A | 2 | a0003c0003t0001g0162a0003c0003t0001g0216 | 2 | HG01952.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1414+2035G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710298 | ||||||
| chr1:207710314
|
G | T | 1 | a0007c0007t0001g0281 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1414+2051G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710314 | ||||||
| chr1:207710347
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1414+2084T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710347 | ||||||
| chr1:207710367
|
G | A | 1 | a0004c0004t0001g0289 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1414+2104G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710367 | ||||||
| chr1:207710509
|
T | G | 1 | a0020c0019t0001g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1414+2246T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710509 | ||||||
| chr1:207710562
|
T | G | 247 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 261 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1414+2299T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710562 | ||||||
| chr1:207710592
|
T | C | 1 | a0002c0002t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1414+2329T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710592 | ||||||
| chr1:207710641
|
G | A | 1 | a0002c0002t0001g0076 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1414+2378G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710641 | ||||||
| chr1:207710706
|
T | G | 2 | a0005c0005t0001g0027a0005c0005t0001g0028 | 2 | HG01192.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1414+2443T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710706 | ||||||
| chr1:207710760
|
C | A | 251 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(248): Show | 266 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1414+2497C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710760 | ||||||
| chr1:207710762
|
G | A | 251 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(248): Show | 266 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1414+2499G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710762 | ||||||
| chr1:207710817
|
A | C | 1 | a0002c0002t0001g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1414+2554A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710817 | ||||||
| chr1:207710824
|
A | G | 8 | a0001c0001t0001g0249a0009c0010t0001g0120a0009c0010t0001g0132others(5): Show | 8 | HG01109.hp2 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1414+2561A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710824 | ||||||
| chr1:207710925
|
A | G | 2 | a0003c0008t0001g0142a0003c0008t0001g0194 | 2 | NA18977.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1414+2662A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710925 | ||||||
| chr1:207710942
|
A | T | 244 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(241): Show | 258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1414+2679A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710942 | ||||||
| chr1:207710947
|
T | C | 244 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(241): Show | 258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1414+2684T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207710947 | ||||||
| chr1:207711239
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1414+2976A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711239 | ||||||
| chr1:207711290
|
A | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1414+3027A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711290 | ||||||
| chr1:207711468
|
T | C | 1 | a0003c0003t0001g0180 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1414+3205T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711468 | ||||||
| chr1:207711489
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0208 | 2 | HG03654.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1414+3226C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711489 | ||||||
| chr1:207711665
|
G | T | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1414+3402G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711665 | ||||||
| chr1:207711707
|
G | T | 1 | a0004c0004t0001g0291 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1414+3444G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711707 | ||||||
| chr1:207711857
|
C | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1414+3594C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711857 | ||||||
| chr1:207711886
|
G | A | 19 | a0001c0001t0001g0134a0001c0001t0001g0171a0001c0001t0001g0231others(16): Show | 24 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1414+3623G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711886 | ||||||
| chr1:207711898
|
C | CAAA | 11 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(8): Show | 11 | HG02258.hp1 HG02258.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1414+3646_1414+364 others(7): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207711898 | |||||
| chr1:207711898
|
CA | C | 9 | a0001c0001t0001g0155a0001c0001t0001g0215a0002c0002t0001g0005others(6): Show | 10 | HG01192.hp1 HG01358.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1414+3648delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207711898 | |||||
| chr1:207711955
|
G | A | 1 | a0002c0002t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1414+3692G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207711955 | ||||||
| chr1:207712134
|
G | A | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1414+3871G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712134 | ||||||
| chr1:207712298
|
T | A | 1 | a0001c0001t0001g0258 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1414+4035T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712298 | ||||||
| chr1:207712500
|
A | G | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1414+4237A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712500 | ||||||
| chr1:207712527
|
T | C | 1 | a0002c0002t0001g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1414+4264T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712527 | ||||||
| chr1:207712536
|
C | T | 224 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1414+4273C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712536 | ||||||
| chr1:207712797
|
C | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1414+4534C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712797 | ||||||
| chr1:207712805
|
C | T | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1414+4542C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712805 | ||||||
| chr1:207712927
|
A | G | 1 | a0007c0007t0001g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1415-4537A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712927 | ||||||
| chr1:207712966
|
G | A | 1 | a0029c0026t0001g0317 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1415-4498G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712966 | ||||||
| chr1:207712967
|
A | G | 10 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415-4497A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712967 | ||||||
| chr1:207712974
|
T | G | 2 | a0002c0002t0001g0074a0002c0002t0001g0113 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1415-4490T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207712974 | ||||||
| chr1:207713079
|
A | G | 4 | a0012c0014t0001g0096a0012c0014t0001g0097a0014c0023t0001g0257others(1): Show | 4 | HG01981.hp1 HG02004.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1415-4385A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713079 | ||||||
| chr1:207713084
|
A | G | 1 | a0003c0003t0001g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1415-4380A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713084 | ||||||
| chr1:207713142
|
A | G | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1415-4322A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713142 | ||||||
| chr1:207713200
|
G | T | 2 | a0001c0001t0001g0232a0018c0021t0001g0268 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1415-4264G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713200 | ||||||
| chr1:207713251
|
G | A | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1415-4213G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713251 | ||||||
| chr1:207713339
|
A | G | 243 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(240): Show | 257 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1415-4125A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713339 | ||||||
| chr1:207713504
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1415-3960G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713504 | ||||||
| chr1:207713697
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1415-3767G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713697 | ||||||
| chr1:207713831
|
C | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1415-3633C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713831 | ||||||
| chr1:207713865
|
C | T | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1415-3599C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713865 | ||||||
| chr1:207713977
|
T | G | 242 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(239): Show | 256 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1415-3487T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713977 | ||||||
| chr1:207713993
|
C | T | 14 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(11): Show | 14 | HG00408.hp2 HG00438.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1415-3471C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207713993 | ||||||
| chr1:207714032
|
C | T | 1 | a0003c0003t0001g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1415-3432C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714032 | ||||||
| chr1:207714107
|
G | A | 1 | a0001c0013t0001g0011 | 2 | NA18947.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1415-3357G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714107 | ||||||
| chr1:207714148
|
A | G | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1415-3316A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714148 | ||||||
| chr1:207714191
|
C | T | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1415-3273C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714191 | ||||||
| chr1:207714311
|
A | G | 12 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1415-3153A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714311 | ||||||
| chr1:207714477
|
G | A | 1 | a0004c0004t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1415-2987G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714477 | ||||||
| chr1:207714651
|
A | C | 230 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1415-2813A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714651 | ||||||
| chr1:207714767
|
G | A | 2 | a0006c0006t0001g0058a0006c0006t0001g0089 | 2 | NA18956.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1415-2697G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714767 | ||||||
| chr1:207714857
|
C | T | 2 | a0002c0002t0001g0080a0006c0006t0001g0060 | 2 | HG02135.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1415-2607C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714857 | ||||||
| chr1:207714946
|
G | A | 1 | a0004c0004t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1415-2518G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714946 | ||||||
| chr1:207714947
|
A | G | 1 | a0004c0004t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1415-2517A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714947 | ||||||
| chr1:207714955
|
A | G | 1 | a0004c0004t0001g0291 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1415-2509A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207714955 | ||||||
| chr1:207715281
|
C | T | 36 | a0003c0003t0001g0002a0003c0003t0001g0007a0003c0003t0001g0157others(33): Show | 39 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1415-2183C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715281 | ||||||
| chr1:207715344
|
G | T | 1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1415-2120G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715344 | ||||||
| chr1:207715359
|
T | C | 36 | a0003c0003t0001g0002a0003c0003t0001g0007a0003c0003t0001g0157others(33): Show | 39 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1415-2105T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715359 | ||||||
| chr1:207715394
|
G | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1415-2070G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715394 | ||||||
| chr1:207715415
|
C | T | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1415-2049C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715415 | ||||||
| chr1:207715719
|
T | C | 10 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415-1745T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715719 | ||||||
| chr1:207715720
|
C | T | 10 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415-1744C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715720 | ||||||
| chr1:207715943
|
T | C | 315 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(312): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1415-1521T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715943 | ||||||
| chr1:207715984
|
C | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0185a0001c0001t0001g0187others(24): Show | 29 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1415-1480C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207715984 | ||||||
| chr1:207716000
|
C | T | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1415-1464C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716000 | ||||||
| chr1:207716013
|
A | G | 2 | a0001c0013t0001g0011a0001c0013t0001g0197 | 3 | NA18947.hp1 NA19002.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1415-1451A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716013 | ||||||
| chr1:207716023
|
G | T | 84 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(81): Show | 88 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1415-1441G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716023 | ||||||
| chr1:207716062
|
A | G | 6 | a0012c0014t0001g0093a0012c0014t0001g0096a0012c0014t0001g0097others(3): Show | 6 | HG01981.hp1 HG02004.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1415-1402A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716062 | ||||||
| chr1:207716139
|
T | G | 5 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0013t0001g0011others(2): Show | 6 | NA18947.hp1 NA19002.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.1415-1325T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716139 | ||||||
| chr1:207716297
|
AGTACAGT | A | 324 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(321): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1415-1158_1415-115 others(11): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207716297 | |||||
| chr1:207716430
|
T | G | 2 | a0004c0004t0001g0324a0004c0004t0001g0326 | 2 | NA18981.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1415-1034T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716430 | ||||||
| chr1:207716493
|
A | AT | 6 | a0012c0014t0001g0093a0012c0014t0001g0096a0012c0014t0001g0097others(3): Show | 6 | HG01981.hp1 HG02004.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1415-964dupT | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207716493 | |||||
| chr1:207716888
|
T | C | 36 | a0003c0003t0001g0002a0003c0003t0001g0007a0003c0003t0001g0157others(33): Show | 39 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1415-576T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716888 | ||||||
| chr1:207716918
|
C | T | 1 | a0025c0030t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1415-546C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716918 | ||||||
| chr1:207716927
|
C | T | 1 | a0002c0002t0001g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1415-537C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207716927 | ||||||
| chr1:207716932
|
TAA | T | 3 | a0001c0001t0001g0223a0002c0002t0001g0045a0005c0036t0001g0015 | 3 | NA18978.hp2 NA18985.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1415-528_1415-527d others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 207716932 | |||||
| chr1:207717130
|
C | T | 198 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(195): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1415-334C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207717130 | ||||||
| chr1:207717191
|
A | T | 1 | a0002c0002t0001g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1415-273A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207717191 | ||||||
| chr1:207717223
|
G | A | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1415-241G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207717223 | ||||||
| chr1:207717423
|
G | A | 2 | a0002c0002t0001g0047a0002c0002t0001g0068 | 2 | HG00738.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1415-41G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207717423 | ||||||
| chr1:207717432
|
A | G | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1415-32A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 10/11 | chr1 | 207717432 | ||||||
| chr1:207717708
|
A | T | 7 | a0009c0010t0001g0120a0009c0010t0001g0132a0009c0010t0001g0133others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1642+17A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207717708 | ||||||
| chr1:207717754
|
T | G | 1 | a0006c0006t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1642+63T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207717754 | ||||||
| chr1:207718166
|
C | T | 6 | a0012c0014t0001g0093a0012c0014t0001g0096a0012c0014t0001g0097others(3): Show | 6 | HG01981.hp1 HG02004.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1642+475C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718166 | ||||||
| chr1:207718208
|
T | C | 7 | a0009c0010t0001g0120a0009c0010t0001g0132a0009c0010t0001g0133others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1642+517T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718208 | ||||||
| chr1:207718234
|
C | T | 12 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1642+543C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718234 | ||||||
| chr1:207718243
|
C | G | 1 | a0009c0010t0001g0328 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1642+552C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718243 | ||||||
| chr1:207718268
|
A | G | 2 | a0002c0002t0001g0077a0002c0002t0001g0106 | 2 | HG01993.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1642+577A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718268 | ||||||
| chr1:207718270
|
T | A | 2 | a0001c0001t0001g0232a0018c0021t0001g0268 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1642+579T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718270 | ||||||
| chr1:207718309
|
G | A | 1 | a0003c0003t0001g0259 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1642+618G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718309 | ||||||
| chr1:207718363
|
C | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1642+672C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718363 | ||||||
| chr1:207718503
|
C | A | 1 | a0003c0003t0001g0259 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1642+812C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718503 | ||||||
| chr1:207718632
|
C | T | 10 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1642+941C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718632 | ||||||
| chr1:207718667
|
C | T | 85 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(82): Show | 89 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1642+976C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718667 | ||||||
| chr1:207718687
|
G | T | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1642+996G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718687 | ||||||
| chr1:207718688
|
T | G | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1642+997T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718688 | ||||||
| chr1:207718742
|
G | C | 1 | a0005c0005t0001g0019 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1642+1051G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718742 | ||||||
| chr1:207718818
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1642+1127T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718818 | ||||||
| chr1:207718944
|
T | A | 2 | a0003c0003t0001g0117a0003c0003t0001g0210 | 2 | HG02071.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1642+1253T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718944 | ||||||
| chr1:207718977
|
A | C | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1642+1286A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207718977 | ||||||
| chr1:207719009
|
C | G | 2 | a0021c0018t0001g0205a0021c0018t0001g0217 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1642+1318C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719009 | ||||||
| chr1:207719120
|
A | T | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1642+1429A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719120 | ||||||
| chr1:207719138
|
C | T | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1642+1447C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719138 | ||||||
| chr1:207719166
|
C | T | 1 | a0003c0003t0001g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1642+1475C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719166 | ||||||
| chr1:207719260
|
TA | T | 264 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(261): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1642+1581delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207719260 | |||||
| chr1:207719262
|
A | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0186 | 3 | HG01515.hp1 HG01517.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1642+1571A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719262 | ||||||
| chr1:207719276
|
T | TA | 97 | a0001c0001t0001g0203a0003c0003t0001g0002a0003c0003t0001g0006others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1642+1596dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207719276 | |||||
| chr1:207719341
|
G | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0252a0001c0001t0001g0255 | 4 | HG01257.hp2 HG01258.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1642+1650G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719341 | ||||||
| chr1:207719361
|
C | T | 1 | a0024c0029t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1642+1670C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719361 | ||||||
| chr1:207719385
|
A | G | 308 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(305): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1642+1694A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719385 | ||||||
| chr1:207719440
|
C | T | 12 | a0001c0001t0001g0155a0001c0001t0001g0209a0002c0002t0001g0005others(9): Show | 13 | HG00597.hp2 HG01192.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1642+1749C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719440 | ||||||
| chr1:207719564
|
A | C | 1 | a0002c0002t0001g0264 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1642+1873A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719564 | ||||||
| chr1:207719719
|
AAC | A | 14 | a0001c0001t0001g0155a0001c0001t0001g0232a0002c0002t0001g0005others(11): Show | 15 | HG01192.hp1 HG01358.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1642+2045_1642+204 others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207719719 | |||||
| chr1:207719741
|
C | G | 1 | a0004c0004t0001g0292 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1642+2050C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719741 | ||||||
| chr1:207719921
|
T | A | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1642+2230T>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207719921 | ||||||
| chr1:207720332
|
CAG | C | 12 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1642+2643_1642+264 others(6): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207720332 | |||||
| chr1:207720347
|
C | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0186 | 3 | HG01515.hp1 HG01517.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1642+2656C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207720347 | ||||||
| chr1:207720367
|
C | T | 2 | a0003c0003t0001g0242a0003c0003t0001g0243 | 2 | HG01070.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1642+2676C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207720367 | ||||||
| chr1:207720437
|
C | T | 36 | a0003c0003t0001g0002a0003c0003t0001g0007a0003c0003t0001g0157others(33): Show | 39 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1642+2746C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207720437 | ||||||
| chr1:207720688
|
C | T | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1643-2930C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207720688 | ||||||
| chr1:207720975
|
CAAG | C | 11 | a0001c0001t0001g0155a0002c0002t0001g0005a0002c0002t0001g0059others(8): Show | 12 | HG01192.hp1 HG01358.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1643-2639_1643-263 others(7): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207720975 | |||||
| chr1:207721071
|
A | G | 197 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1643-2547A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721071 | ||||||
| chr1:207721112
|
A | G | 1 | a0002c0002t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1643-2506A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721112 | ||||||
| chr1:207721240
|
G | T | 4 | a0002c0002t0001g0054a0002c0002t0001g0076a0002c0002t0001g0077others(1): Show | 4 | HG00741.hp1 HG01175.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1643-2378G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721240 | ||||||
| chr1:207721280
|
GTGCTGCA others(34): Show |
G | 1 | a0003c0003t0001g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1643-2337_1643-229 others(45): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721280 | ||||||
| chr1:207721302
|
A | G | 1 | a0005c0005t0001g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1643-2316A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721302 | ||||||
| chr1:207721326
|
A | G | 12 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1643-2292A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721326 | ||||||
| chr1:207721342
|
C | G | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1643-2276C>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721342 | ||||||
| chr1:207721343
|
T | C | 2 | a0006c0006t0001g0327a0013c0011t0001g0199 | 2 | HG03209.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1643-2275T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721343 | ||||||
| chr1:207721343
|
T | TC | 8 | a0001c0001t0001g0218a0002c0002t0001g0176a0003c0003t0001g0157others(5): Show | 8 | HG01433.hp1 HG01496.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1643-2269dupC | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207721343 | |||||
| chr1:207721353
|
C | T | 1 | a0003c0003t0001g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1643-2265C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721353 | ||||||
| chr1:207721566
|
C | A | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0136others(47): Show | 54 | HG00558.hp1 HG00738.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1643-2052C>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721566 | ||||||
| chr1:207721646
|
A | C | 1 | a0003c0003t0001g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1643-1972A>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721646 | ||||||
| chr1:207721663
|
T | G | 2 | a0007c0007t0001g0119a0007c0007t0001g0275 | 2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1643-1955T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721663 | ||||||
| chr1:207721739
|
C | T | 1 | a0002c0002t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1643-1879C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721739 | ||||||
| chr1:207721750
|
C | T | 1 | a0002c0002t0001g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1643-1868C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721750 | ||||||
| chr1:207721751
|
G | C | 2 | a0002c0002t0001g0073a0004c0004t0001g0321 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1643-1867G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721751 | ||||||
| chr1:207721762
|
G | A | 1 | a0007c0007t0001g0277 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1643-1856G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721762 | ||||||
| chr1:207721995
|
G | A | 3 | a0001c0001t0001g0278a0025c0030t0001g0118a0032c0038t0001g0173 | 3 | HG02615.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1643-1623G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721995 | ||||||
| chr1:207721995
|
G | T | 1 | a0003c0003t0001g0165 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1643-1623G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207721995 | ||||||
| chr1:207722019
|
A | G | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1643-1599A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722019 | ||||||
| chr1:207722058
|
ATTTG | A | 6 | a0012c0014t0001g0093a0012c0014t0001g0096a0012c0014t0001g0097others(3): Show | 6 | HG01981.hp1 HG02004.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1643-1555_1643-155 others(8): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207722058 | |||||
| chr1:207722116
|
C | T | 13 | a0001c0001t0001g0139a0007c0007t0001g0119a0007c0007t0001g0129others(10): Show | 13 | HG01261.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1643-1502C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722116 | ||||||
| chr1:207722171
|
T | G | 1 | a0003c0003t0001g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1643-1447T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722171 | ||||||
| chr1:207722180
|
G | C | 1 | a0003c0003t0001g0242 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1643-1438G>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722180 | ||||||
| chr1:207722204
|
C | T | 7 | a0009c0010t0001g0120a0009c0010t0001g0132a0009c0010t0001g0133others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1643-1414C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722204 | ||||||
| chr1:207722214
|
ATTTTGTC | A | 11 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0154others(8): Show | 11 | HG00408.hp2 HG00438.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1643-1397_1643-139 others(11): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207722214 | |||||
| chr1:207722232
|
G | A | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1643-1386G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722232 | ||||||
| chr1:207722267
|
T | C | 101 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(98): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1643-1351T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722267 | ||||||
| chr1:207722351
|
C | T | 308 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(305): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1643-1267C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722351 | ||||||
| chr1:207722527
|
G | A | 1 | a0004c0004t0001g0288 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1643-1091G>A | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722527 | ||||||
| chr1:207722599
|
T | G | 1 | a0003c0003t0001g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1643-1019T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722599 | ||||||
| chr1:207722768
|
A | G | 1 | a0004c0004t0001g0325 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1643-850A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722768 | ||||||
| chr1:207722786
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1643-832A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722786 | ||||||
| chr1:207722812
|
T | TC | 97 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1643-805dupC | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207722812 | |||||
| chr1:207722922
|
C | T | 2 | a0007c0007t0001g0281a0018c0021t0001g0266 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1643-696C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722922 | ||||||
| chr1:207722991
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1643-627T>C | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207722991 | ||||||
| chr1:207723032
|
A | T | 1 | a0003c0003t0001g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1643-586A>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207723032 | ||||||
| chr1:207723033
|
T | G | 1 | a0003c0003t0001g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1643-585T>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207723033 | ||||||
| chr1:207723126
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1643-492C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207723126 | ||||||
| chr1:207723225
|
A | G | 1 | a0031c0025t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1643-393A>G | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207723225 | ||||||
| chr1:207723297
|
G | T | 1 | a0006c0006t0001g0056 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1643-321G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207723297 | ||||||
| chr1:207723300
|
C | T | 1 | a0004c0004t0001g0291 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1643-318C>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207723300 | ||||||
| chr1:207723421
|
C | CA | 33 | a0001c0001t0001g0139a0001c0001t0001g0155a0001c0001t0001g0209others(30): Show | 34 | HG00597.hp2 HG01175.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.1643-179dupA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207723421 | |||||
| chr1:207723421
|
CA | C | 15 | a0001c0001t0001g0134a0001c0001t0001g0231a0001c0013t0001g0197others(12): Show | 15 | HG01109.hp2 HG01168.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.1643-179delA | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207723421 | |||||
| chr1:207723421
|
CAA | C | 10 | a0007c0007t0001g0119a0007c0007t0001g0129a0007c0007t0001g0130others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1643-180_1643-179d others(4): Show |
CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 207723421 | |||||
| chr1:207723549
|
G | T | 1 | a0003c0003t0001g0162 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1643-69G>T | CR1L | ENSG00000197721.17 | transcript | ENST00000508064.7 | protein_coding | 11/11 | chr1 | 207723549 |