Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1407 |
|---|---|
| ensemblid | ENSG00000008405.12 |
| hgncid | 2384 |
| symbol | CRY1 |
| name | cryptochrome circadian regulator 1 |
| refseq_nuc | NM_004075.5 |
| refseq_prot | NP_004066.1 |
| ensembl_nuc | ENST00000008527.10 |
| ensembl_prot | ENSP00000008527.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 106991364 |
| end | 107093549 |
| strand | - |
| ver | v1.2 |
| region | chr12:106991364-107093549 |
| region5000 | chr12:106986364-107098549 |
| regionname0 | CRY1_chr12_106991364_107093549 |
| regionname5000 | CRY1_chr12_106986364_107098549 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 586 | 319 | 76 | 61 | 134 | 8 | 38 | 108 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0002 | 0/0 | 586 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| 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 | 1761 | 256 | 59 | 47 | 118 | 5 | 27 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| c0002 | 1/1 | 1761 | 57 | 12 | 14 | 15 | 3 | 11 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| c0003 | 0/0 | 1761 | 4 | 4 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| c0004 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| c0005 | 0/0 | 1761 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| c0006 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1227 | 144 | 11 | 32 | 78 | 5 | 18 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0002 | 0/0 | 1227 | 75 | 20 | 11 | 35 | 0 | 9 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0003 | 1/1 | 1227 | 60 | 16 | 14 | 15 | 3 | 10 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0004 | 0/0 | 1227 | 16 | 14 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0005 | 0/0 | 1227 | 5 | 5 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0006 | 0/0 | 1227 | 4 | 4 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0007 | 0/0 | 1227 | 3 | 3 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0008 | 0/0 | 1227 | 3 | 2 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0009 | 0/0 | 1227 | 2 | 0 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0010 | 0/0 | 1227 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0011 | 0/0 | 1227 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0012 | 0/0 | 1227 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0013 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0014 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| t0015 | 0/0 | 1227 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| 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 | 3 | 1 | 0 | 0 | 1 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| 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 | 1761 | 256 | 59 | 47 | 118 | 5 | 27 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0002 | 1/1 | 1761 | 57 | 12 | 14 | 15 | 3 | 11 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0003 | 0/0 | 1761 | 4 | 4 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0004 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0006 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0002c0005 | 0/0 | 1761 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2987 | 143 | 11 | 32 | 77 | 5 | 18 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0002 | 0/0 | 2987 | 73 | 19 | 10 | 35 | 0 | 9 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0003 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0004 | 0/0 | 2987 | 16 | 14 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0005 | 0/0 | 2987 | 5 | 5 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0007 | 0/0 | 2987 | 3 | 3 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0008 | 0/0 | 2987 | 3 | 2 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0009 | 0/0 | 2987 | 2 | 0 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0010 | 0/0 | 2987 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0011 | 0/0 | 2987 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0013 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0014 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0001t0015 | 0/0 | 2987 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0002t0003 | 1/1 | 2987 | 56 | 12 | 14 | 15 | 3 | 10 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0002t0012 | 0/0 | 2987 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0003t0006 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0004t0002 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0001c0006t0001 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| a0002c0005t0002 | 0/0 | 2987 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | copy fasta | chr12 | 106986364 | 107098549 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0010g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0010g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0011g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0011g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0015g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0012g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0003t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0003t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0003t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0003t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0004t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0002c0005t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0181 | EUR | GBR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0226 | EUR | GBR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0214 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0180 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00673 | hp1 | a0001 | c0001 | t0014 | g0272 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0179 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0068 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0177 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0201 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0202 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0067 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0218 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0198 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0195 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0164 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0176 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01243 | hp2 | a0001 | c0001 | t0015 | g0309 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0219 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0197 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0196 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0209 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0200 | EUR | IBS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0169 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01928 | hp2 | a0002 | c0005 | t0002 | g0282 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0206 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02027 | hp2 | a0001 | c0001 | t0008 | g0152 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0221 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0189 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02155 | hp1 | a0001 | c0001 | t0011 | g0246 | EAS | CDX | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0288 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0220 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0178 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0203 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0174 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02622 | hp2 | a0001 | c0003 | t0006 | g0160 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0171 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02647 | hp2 | a0001 | c0003 | t0006 | g0157 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0216 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02717 | hp2 | a0001 | c0003 | t0006 | g0159 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0208 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0210 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0207 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0199 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0204 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03486 | hp2 | a0001 | c0003 | t0006 | g0158 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0217 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0215 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0173 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0227 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03688 | hp2 | a0001 | c0002 | t0012 | g0011 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0211 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0222 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0229 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0228 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CHB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18941 | hp2 | a0001 | c0001 | t0010 | g0037 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18990 | hp1 | a0001 | c0001 | t0011 | g0245 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0223 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | LWK | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19062 | hp2 | a0001 | c0006 | t0001 | g0069 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0045 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0191 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | ASW | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ASW | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | GIH | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0234 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | USA | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0194 | AFR | LWK | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | LWK | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0175 | REF | REF | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0212 | REF | REF | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106997930
|
T | C | 1 | a0002 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1274A>G | p.Asn425Ser | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 8/13 | 1862/2987 | 1274/1761 | 425/586 | chr12 | 106997930 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106997370
|
T | C | 1 | a0001c0004 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1509A>G | p.Val503Val | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/13 | 2097/2987 | 1509/1761 | 503/586 | chr12 | 106997370 | ||
| chr12:106997376
|
T | A | 1 | a0001c0003 | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.1503A>T | p.Ala501Ala | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/13 | 2091/2987 | 1503/1761 | 501/586 | chr12 | 106997376 | ||
| chr12:107001328
|
A | G | 5 | a0001c0001a0001c0003a0001c0004others(2): Show | 263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
synonymous_variant | LOW | c.636T>C | p.Gly212Gly | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/13 | 1224/2987 | 636/1761 | 212/586 | chr12 | 107001328 | ||
| chr12:107001852
|
T | G | 1 | a0001c0006 | 1 | NA19062.hp2 | synonymous_variant | LOW | c.507A>C | p.Thr169Thr | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/13 | 1095/2987 | 507/1761 | 169/586 | chr12 | 107001852 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106991506
|
T | C | 1 | a0001c0001t0011 | 2 | HG02155.hp1 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*496A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1281 | chr12 | 106991506 | |||||
| chr12:106991586
|
C | T | 2 | a0001c0001t0004a0001c0001t0013 | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1201 | chr12 | 106991586 | |||||
| chr12:106991658
|
C | T | 1 | a0001c0001t0007 | 3 | HG02818.hp1 HG03139.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*344G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1129 | chr12 | 106991658 | |||||
| chr12:106991676
|
T | G | 1 | a0001c0001t0009 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1111 | chr12 | 106991676 | |||||
| chr12:106991715
|
T | A | 1 | a0001c0001t0010 | 2 | NA18941.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*287A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1072 | chr12 | 106991715 | |||||
| chr12:106991778
|
T | C | 1 | a0001c0001t0014 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1009 | chr12 | 106991778 | |||||
| chr12:106991832
|
C | A | 7 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(4): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*170G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 955 | chr12 | 106991832 | |||||
| chr12:107092978
|
G | A | 1 | a0001c0001t0013 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 17 | chr12 | 107092978 | |||||
| chr12:107093085
|
G | A | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0014others(2): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-124C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 124 | chr12 | 107093085 | |||||
| chr12:107093134
|
C | T | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
5_prime_UTR_variant | MODIFIER | c.-173G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 173 | chr12 | 107093134 | |||||
| chr12:107093269
|
G | A | 6 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(3): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-308C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 308 | chr12 | 107093269 | |||||
| chr12:107093291
|
C | T | 5 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(2): Show | 151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-330G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 330 | chr12 | 107093291 | |||||
| chr12:107093296
|
A | G | 1 | a0001c0002t0012 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-335T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 335 | chr12 | 107093296 | |||||
| chr12:107093483
|
G | A | 1 | a0001c0001t0015 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-522C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 522 | chr12 | 107093483 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106992158
|
T | C | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.*1-157A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992158 | ||||||
| chr12:106992332
|
C | T | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*1-331G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992332 | ||||||
| chr12:106992398
|
A | C | 1 | a0001c0001t0002g0276 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1761+389T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992398 | ||||||
| chr12:106992507
|
A | G | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1761+280T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992507 | ||||||
| chr12:106992608
|
C | G | 1 | a0001c0002t0003g0218 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1761+179G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992608 | ||||||
| chr12:106992617
|
A | C | 1 | a0001c0002t0003g0218 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1761+170T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992617 | ||||||
| chr12:106992760
|
C | T | 1 | a0001c0002t0003g0196 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1761+27G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992760 | ||||||
| chr12:106992907
|
T | A | 1 | a0001c0001t0002g0286 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1658-17A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 11/12 | chr12 | 106992907 | ||||||
| chr12:106992962
|
T | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01167.hp2 HG01169.hp1 |
splice_region_variant&intron_variant | LOW | c.1657+3A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 11/12 | chr12 | 106992962 | ||||||
| chr12:106993247
|
A | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 174 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1586-211T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993247 | ||||||
| chr12:106993277
|
C | T | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1586-241G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993277 | ||||||
| chr12:106993308
|
G | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0009g0067others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1586-272C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993308 | ||||||
| chr12:106993385
|
C | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1586-349G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993385 | ||||||
| chr12:106993588
|
G | A | 7 | a0001c0001t0002g0248a0001c0001t0002g0261a0001c0001t0002g0263others(4): Show | 7 | HG01123.hp1 HG01433.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1586-552C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993588 | ||||||
| chr12:106993648
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0116others(2): Show | 6 | HG01192.hp1 HG01934.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1586-612G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993648 | ||||||
| chr12:106993704
|
C | T | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1586-668G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993704 | ||||||
| chr12:106993705
|
G | A | 5 | a0001c0001t0002g0243a0001c0001t0002g0302a0001c0001t0002g0303others(2): Show | 5 | HG03195.hp1 HG03579.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1586-669C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993705 | ||||||
| chr12:106993709
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1586-673A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993709 | ||||||
| chr12:106993847
|
C | T | 1 | a0001c0002t0003g0187 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1586-811G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993847 | ||||||
| chr12:106994052
|
A | G | 1 | a0001c0001t0002g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1586-1016T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994052 | ||||||
| chr12:106994059
|
AAAAC | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0233a0001c0001t0005g0234 | 3 | HG02109.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1586-1027_1586-102 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994059 | ||||||
| chr12:106994111
|
T | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1586-1075A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994111 | ||||||
| chr12:106994119
|
A | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1586-1083T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994119 | ||||||
| chr12:106994691
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1586-1655G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994691 | ||||||
| chr12:106994732
|
A | G | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1586-1696T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994732 | ||||||
| chr12:106994770
|
C | A | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1586-1734G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994770 | ||||||
| chr12:106994830
|
A | G | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1586-1794T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994830 | ||||||
| chr12:106994847
|
C | T | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1586-1811G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994847 | ||||||
| chr12:106995168
|
AAT | A | 1 | a0001c0001t0001g0001 | 3 | HG01516.hp1 HG06807.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1585+2124_1585+212 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995168 | ||||||
| chr12:106995295
|
A | G | 1 | a0001c0001t0004g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1585+1999T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995295 | ||||||
| chr12:106995305
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1585+1989C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995305 | ||||||
| chr12:106995475
|
T | C | 1 | a0001c0002t0003g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1585+1819A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995475 | ||||||
| chr12:106995746
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1585+1548G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995746 | ||||||
| chr12:106995818
|
C | A | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1585+1476G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995818 | ||||||
| chr12:106995907
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1585+1387C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995907 | ||||||
| chr12:106996004
|
C | T | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1585+1290G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996004 | ||||||
| chr12:106996178
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1585+1116A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996178 | ||||||
| chr12:106996204
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1585+1090G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996204 | ||||||
| chr12:106996403
|
G | T | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1585+891C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996403 | ||||||
| chr12:106996436
|
G | C | 1 | a0001c0001t0001g0017 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1585+858C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996436 | ||||||
| chr12:106996475
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1585+819C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996475 | ||||||
| chr12:106996793
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1585+501T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996793 | ||||||
| chr12:106996906
|
T | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1585+388A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996906 | ||||||
| chr12:106996971
|
C | A | 1 | a0001c0001t0002g0264 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1585+323G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996971 | ||||||
| chr12:106996972
|
A | T | 1 | a0001c0001t0002g0264 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1585+322T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996972 | ||||||
| chr12:106997089
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1585+205G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106997089 | ||||||
| chr12:106997133
|
G | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1585+161C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106997133 | ||||||
| chr12:106997890
|
T | C | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289+25A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 8/12 | chr12 | 106997890 | ||||||
| chr12:106998154
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1138-88C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998154 | ||||||
| chr12:106998169
|
C | A | 1 | a0001c0001t0002g0294 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1138-103G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998169 | ||||||
| chr12:106998346
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1138-280C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998346 | ||||||
| chr12:106998389
|
C | T | 1 | a0001c0001t0002g0294 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1138-323G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998389 | ||||||
| chr12:106998399
|
A | T | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1138-333T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998399 | ||||||
| chr12:106998543
|
G | A | 2 | a0001c0001t0007g0023a0001c0001t0007g0024 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1138-477C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998543 | ||||||
| chr12:106998587
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1138-521A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998587 | ||||||
| chr12:106998659
|
A | AAC | 22 | a0001c0001t0001g0013a0001c0001t0001g0093a0001c0001t0001g0102others(19): Show | 23 | HG00408.hp2 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1138-595_1138-594d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | AACAC | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 85 | HG00408.hp1 HG00609.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.1138-597_1138-594d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | AACACAC | 23 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 25 | HG00597.hp1 HG02027.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.1138-599_1138-594d others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | AACACACA others(1): Show |
40 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 41 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1138-601_1138-594d others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | AACACACA others(3): Show |
12 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0052others(9): Show | 12 | HG02109.hp1 HG02572.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1138-603_1138-594d others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | AACACACA others(5): Show |
10 | a0001c0001t0002g0237a0001c0001t0002g0239a0001c0001t0002g0253others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1138-605_1138-594d others(14): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | AACACACA others(7): Show |
30 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0236others(27): Show | 32 | HG00558.hp1 HG01123.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.1138-607_1138-594d others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | AACACACA others(9): Show |
27 | a0001c0001t0002g0235a0001c0001t0002g0238a0001c0001t0002g0240others(24): Show | 27 | HG00558.hp2 HG00673.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1138-609_1138-594d others(18): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | AACACACA others(11): Show |
3 | a0001c0001t0002g0241a0001c0001t0002g0273a0001c0001t0002g0289 | 3 | HG02145.hp1 HG02735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1138-611_1138-594d others(20): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0002g0277 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1138-594_1138-593i others(17): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998659
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0002g0268 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1138-594_1138-593i others(19): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | ||||||
| chr12:106998679
|
C | CACACACA others(7): Show |
1 | a0001c0001t0002g0307 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1138-614_1138-613i others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998679 | ||||||
| chr12:106998693
|
A | C | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(11): Show | 16 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1138-627T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998693 | ||||||
| chr12:106998790
|
C | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1138-724G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998790 | ||||||
| chr12:106998857
|
A | G | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1137+694T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998857 | ||||||
| chr12:106998867
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1137+684T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998867 | ||||||
| chr12:106998932
|
C | G | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137+619G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998932 | ||||||
| chr12:106998939
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18973.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1137+612C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998939 | ||||||
| chr12:106999000
|
T | C | 99 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(96): Show | 103 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(100): Show |
intron_variant | MODIFIER | c.1137+551A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999000 | ||||||
| chr12:106999043
|
C | CA | 24 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0089others(21): Show | 25 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1137+507dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999043 | ||||||
| chr12:106999073
|
G | A | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1137+478C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999073 | ||||||
| chr12:106999266
|
T | C | 5 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0252others(2): Show | 7 | HG00558.hp1 HG03688.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137+285A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999266 | ||||||
| chr12:106999274
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1137+277G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999274 | ||||||
| chr12:106999374
|
C | G | 1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1137+177G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999374 | ||||||
| chr12:106999412
|
G | A | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1137+139C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999412 | ||||||
| chr12:106999894
|
A | T | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.826-32T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 6/12 | chr12 | 106999894 | ||||||
| chr12:107000270
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.685-188G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000270 | ||||||
| chr12:107000300
|
TAAATTTC others(4): Show |
T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0063others(3): Show | 9 | HG01069.hp1 HG01071.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-229_685-219del others(11): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000300 | ||||||
| chr12:107000322
|
C | CAGAA | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-244_685-241dup others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000322 | ||||||
| chr12:107000356
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.685-274A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000356 | ||||||
| chr12:107000840
|
G | A | 1 | a0001c0002t0003g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.684+440C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000840 | ||||||
| chr12:107001143
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.684+137C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107001143 | ||||||
| chr12:107001452
|
G | A | 1 | a0001c0001t0002g0294 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.596-84C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001452 | ||||||
| chr12:107001512
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.596-144A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001512 | ||||||
| chr12:107001570
|
G | T | 4 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287others(1): Show | 4 | HG02602.hp1 NA18943.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+194C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001570 | ||||||
| chr12:107001659
|
T | C | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.595+105A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001659 | ||||||
| chr12:107001735
|
G | A | 3 | a0001c0002t0003g0199a0001c0002t0003g0208a0001c0002t0003g0210 | 3 | HG02922.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.595+29C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001735 | ||||||
| chr12:107001960
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.411-12C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107001960 | ||||||
| chr12:107002257
|
G | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0109a0001c0001t0001g0112others(1): Show | 4 | HG00639.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-309C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002257 | ||||||
| chr12:107002355
|
G | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.411-407C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002355 | ||||||
| chr12:107002575
|
T | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.411-627A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002575 | ||||||
| chr12:107002627
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.411-679A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002627 | ||||||
| chr12:107002957
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.411-1009C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002957 | ||||||
| chr12:107002998
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.411-1050C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002998 | ||||||
| chr12:107003019
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.411-1071C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003019 | ||||||
| chr12:107003043
|
C | T | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411-1095G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003043 | ||||||
| chr12:107003354
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.411-1406A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003354 | ||||||
| chr12:107003405
|
T | C | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411-1457A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003405 | ||||||
| chr12:107003450
|
C | T | 3 | a0001c0002t0003g0199a0001c0002t0003g0208a0001c0002t0003g0210 | 3 | HG02922.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.411-1502G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003450 | ||||||
| chr12:107003736
|
T | A | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.410+1370A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003736 | ||||||
| chr12:107003807
|
A | AT | 12 | a0001c0001t0001g0093a0001c0001t0001g0145a0001c0001t0001g0146others(9): Show | 13 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.410+1298dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003807 | ||||||
| chr12:107003807
|
AT | A | 83 | a0001c0001t0001g0020a0001c0001t0002g0009a0001c0001t0002g0010others(80): Show | 86 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.410+1298delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003807 | ||||||
| chr12:107003810
|
T | G | 1 | a0001c0001t0002g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.410+1296A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003810 | ||||||
| chr12:107003896
|
T | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.410+1210A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003896 | ||||||
| chr12:107003899
|
C | T | 83 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(80): Show | 85 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(82): Show |
intron_variant | MODIFIER | c.410+1207G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003899 | ||||||
| chr12:107003900
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.410+1206C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003900 | ||||||
| chr12:107003919
|
C | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.410+1187G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003919 | ||||||
| chr12:107004097
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.410+1009C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004097 | ||||||
| chr12:107004103
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.410+1003G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004103 | ||||||
| chr12:107004445
|
G | C | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+661C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004445 | ||||||
| chr12:107004589
|
A | G | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.410+517T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004589 | ||||||
| chr12:107004987
|
C | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.410+119G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004987 | ||||||
| chr12:107005003
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.410+103A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107005003 | ||||||
| chr12:107005340
|
T | G | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0284 | 3 | NA18940.hp1 NA19079.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.268-92A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005340 | ||||||
| chr12:107005353
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.268-105G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005353 | ||||||
| chr12:107005498
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.268-250A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005498 | ||||||
| chr12:107005525
|
C | T | 2 | a0001c0002t0003g0201a0001c0002t0003g0202 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.268-277G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005525 | ||||||
| chr12:107005655
|
C | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 153 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.268-407G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005655 | ||||||
| chr12:107005929
|
A | C | 1 | a0001c0002t0003g0215 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.268-681T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005929 | ||||||
| chr12:107006107
|
G | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.268-859C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006107 | ||||||
| chr12:107006362
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.268-1114G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006362 | ||||||
| chr12:107006372
|
T | C | 3 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0155 | 4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1124A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006372 | ||||||
| chr12:107006375
|
CA | C | 5 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(2): Show | 6 | HG00673.hp1 HG02280.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-1128delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006375 | ||||||
| chr12:107006531
|
T | C | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.268-1283A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006531 | ||||||
| chr12:107006536
|
T | C | 3 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0155 | 4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1288A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006536 | ||||||
| chr12:107006638
|
C | CG | 67 | a0001c0001t0002g0010a0001c0001t0002g0235a0001c0001t0002g0236others(64): Show | 68 | HG00558.hp1 HG00558.hp2 HG01123.hp1 others(65): Show |
intron_variant | MODIFIER | c.268-1391_268-1390i others(3): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006638 | ||||||
| chr12:107006638
|
C | CGT | 35 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(32): Show | 38 | HG00673.hp1 HG01175.hp1 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.268-1391_268-1390i others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006638 | ||||||
| chr12:107006638
|
C | CGTT | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 129 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.268-1391_268-1390i others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006638 | ||||||
| chr12:107006638
|
C | CGTTT | 17 | a0001c0001t0001g0015a0001c0001t0001g0049a0001c0001t0001g0071others(14): Show | 17 | HG00408.hp1 HG01175.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-1391_268-1390i others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006638 | ||||||
| chr12:107006644
|
T | G | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.268-1396A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006644 | ||||||
| chr12:107006681
|
AGGCTGAA others(7): Show |
A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.268-1447_268-1434d others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006681 | ||||||
| chr12:107006704
|
T | A | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.268-1456A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006704 | ||||||
| chr12:107006739
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.268-1491G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006739 | ||||||
| chr12:107006912
|
G | A | 6 | a0001c0001t0004g0156a0001c0001t0004g0164a0001c0001t0004g0165others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-1664C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006912 | ||||||
| chr12:107006924
|
G | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.268-1676C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006924 | ||||||
| chr12:107006976
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.268-1728T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006976 | ||||||
| chr12:107007122
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.268-1874C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007122 | ||||||
| chr12:107007134
|
C | T | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1886G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007134 | ||||||
| chr12:107007142
|
C | T | 2 | a0001c0001t0007g0023a0001c0001t0007g0024 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.268-1894G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007142 | ||||||
| chr12:107007227
|
G | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0133 | 3 | HG00408.hp2 NA18967.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.268-1979C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007227 | ||||||
| chr12:107007232
|
A | G | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-1984T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007232 | ||||||
| chr12:107007530
|
CT | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0120others(4): Show | 7 | HG01069.hp1 HG01070.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.268-2283delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007530 | ||||||
| chr12:107007533
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.268-2285A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007533 | ||||||
| chr12:107007555
|
G | C | 1 | a0002c0005t0002g0282 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.268-2307C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007555 | ||||||
| chr12:107007792
|
C | T | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-2544G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007792 | ||||||
| chr12:107007830
|
C | T | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.268-2582G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007830 | ||||||
| chr12:107007991
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.268-2743A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007991 | ||||||
| chr12:107008216
|
A | G | 2 | a0001c0002t0003g0180a0001c0002t0003g0181 | 2 | HG00099.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.268-2968T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008216 | ||||||
| chr12:107008274
|
A | G | 2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.268-3026T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008274 | ||||||
| chr12:107008545
|
T | C | 1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.268-3297A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008545 | ||||||
| chr12:107008769
|
T | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.268-3521A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008769 | ||||||
| chr12:107008776
|
T | C | 1 | a0001c0001t0002g0285 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.268-3528A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008776 | ||||||
| chr12:107008778
|
G | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.268-3530C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008778 | ||||||
| chr12:107008829
|
G | A | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-3581C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008829 | ||||||
| chr12:107008833
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.268-3585C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008833 | ||||||
| chr12:107008911
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.268-3663A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008911 | ||||||
| chr12:107008934
|
T | C | 2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.268-3686A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008934 | ||||||
| chr12:107008935
|
C | T | 1 | a0001c0001t0004g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.268-3687G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008935 | ||||||
| chr12:107008946
|
T | C | 1 | a0001c0001t0002g0276 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.268-3698A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008946 | ||||||
| chr12:107009017
|
G | A | 1 | a0001c0001t0002g0259 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.268-3769C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009017 | ||||||
| chr12:107009313
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.268-4065G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009313 | ||||||
| chr12:107009421
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.268-4173A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009421 | ||||||
| chr12:107009491
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.268-4243C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009491 | ||||||
| chr12:107009525
|
C | A | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-4277G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009525 | ||||||
| chr12:107009558
|
A | C | 1 | a0001c0001t0001g0131 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.268-4310T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009558 | ||||||
| chr12:107009559
|
A | C | 4 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0081others(1): Show | 4 | HG01243.hp1 HG01257.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-4311T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009559 | ||||||
| chr12:107009560
|
A | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.268-4312T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009560 | ||||||
| chr12:107009561
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.268-4313T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009561 | ||||||
| chr12:107009562
|
ACATATAT others(2): Show |
A | 12 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0048others(9): Show | 13 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.268-4323_268-4315d others(11): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009562 | ||||||
| chr12:107009562
|
ACATATAT others(4): Show |
A | 41 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 42 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.268-4325_268-4315d others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009562 | ||||||
| chr12:107009562
|
ACATATAT others(6): Show |
A | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.268-4327_268-4315d others(15): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009562 | ||||||
| chr12:107009563
|
C | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(88): Show | 95 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.268-4315G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CAT | 11 | a0001c0002t0003g0177a0001c0002t0003g0178a0001c0002t0003g0179others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.268-4317_268-4316d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATAT | 8 | a0001c0001t0004g0154a0001c0001t0005g0232a0001c0001t0013g0171others(5): Show | 9 | HG01257.hp2 HG02647.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.268-4319_268-4316d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATAT | 12 | a0001c0002t0003g0182a0001c0002t0003g0188a0001c0002t0003g0189others(9): Show | 12 | HG01074.hp1 HG01099.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.268-4321_268-4316d others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATATA others(1): Show |
7 | a0001c0002t0003g0174a0001c0002t0003g0175a0001c0002t0003g0180others(4): Show | 7 | HG00642.hp1 HG01255.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-4323_268-4316d others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATATA others(3): Show |
6 | a0001c0002t0003g0181a0001c0002t0003g0183a0001c0002t0003g0198others(3): Show | 6 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-4325_268-4316d others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATATA others(5): Show |
6 | a0001c0001t0003g0225a0001c0001t0004g0163a0001c0002t0003g0172others(3): Show | 6 | HG02572.hp1 HG03540.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-4327_268-4316d others(14): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATATA others(7): Show |
5 | a0001c0001t0003g0193a0001c0001t0003g0224a0001c0002t0003g0176others(2): Show | 5 | HG01192.hp2 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.268-4329_268-4316d others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATATA others(9): Show |
2 | a0001c0002t0003g0206a0001c0003t0006g0158 | 2 | HG02027.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.268-4331_268-4316d others(18): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATATA others(11): Show |
7 | a0001c0001t0004g0007a0001c0001t0004g0162a0001c0001t0005g0233others(4): Show | 8 | HG00140.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-4333_268-4316d others(20): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATATA others(13): Show |
1 | a0001c0002t0012g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.268-4335_268-4316d others(22): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009563
|
C | CATATATA others(23): Show |
1 | a0001c0002t0003g0184 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.268-4345_268-4316d others(32): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | ||||||
| chr12:107009565
|
T | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(85): Show | 92 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.268-4317A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009565 | ||||||
| chr12:107009565
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0138a0001c0001t0001g0150 | 3 | HG01123.hp2 HG03486.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.268-4317A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009565 | ||||||
| chr12:107009566
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.268-4329_268-4319d others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009566 | ||||||
| chr12:107009567
|
T | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(85): Show | 92 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.268-4319A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009567 | ||||||
| chr12:107009569
|
T | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(62): Show | 67 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.268-4321A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009569 | ||||||
| chr12:107009571
|
T | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-4323A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009571 | ||||||
| chr12:107009573
|
T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0048others(11): Show | 15 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.268-4325A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009573 | ||||||
| chr12:107009575
|
T | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.268-4327A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009575 | ||||||
| chr12:107009577
|
T | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 41 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.268-4329A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009577 | ||||||
| chr12:107009579
|
T | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00140.hp2 HG01123.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.268-4331A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009579 | ||||||
| chr12:107009581
|
T | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0151others(1): Show | 4 | HG02559.hp1 HG02818.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-4333A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009581 | ||||||
| chr12:107009581
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0004g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.268-4355_268-4334d others(24): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009581 | ||||||
| chr12:107009583
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.268-4335A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009583 | ||||||
| chr12:107009583
|
TATATATA others(13): Show |
T | 72 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(69): Show | 74 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.268-4355_268-4336d others(22): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009583 | ||||||
| chr12:107009585
|
TATATATA others(11): Show |
T | 11 | a0001c0001t0002g0262a0001c0001t0002g0295a0001c0001t0002g0296others(8): Show | 11 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.268-4355_268-4338d others(20): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009585 | ||||||
| chr12:107009587
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.268-4355_268-4340d others(18): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009587 | ||||||
| chr12:107009589
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0002g0294 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.268-4355_268-4342d others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009589 | ||||||
| chr12:107009591
|
TATATATA others(5): Show |
T | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-4355_268-4344d others(14): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009591 | ||||||
| chr12:107009593
|
TATATATA others(3): Show |
T | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(72): Show | 78 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.268-4355_268-4346d others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009593 | ||||||
| chr12:107009595
|
TATATATA others(1): Show |
T | 8 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0083others(5): Show | 10 | HG01081.hp1 HG01243.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.268-4355_268-4348d others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009595 | ||||||
| chr12:107009599
|
TATAA | T | 5 | a0001c0001t0004g0161a0001c0001t0008g0169a0001c0001t0008g0170others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-4355_268-4352d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009599 | ||||||
| chr12:107009603
|
A | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(63): Show | 69 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.268-4355T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009603 | ||||||
| chr12:107010028
|
G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0041 | 2 | HG02132.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.268-4780C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010028 | ||||||
| chr12:107010074
|
T | A | 1 | a0001c0001t0004g0163 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.268-4826A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010074 | ||||||
| chr12:107010134
|
T | TTTTCA | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.268-4891_268-4887d others(7): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010134 | ||||||
| chr12:107010481
|
C | T | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.268-5233G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010481 | ||||||
| chr12:107010514
|
G | A | 76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.268-5266C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010514 | ||||||
| chr12:107010525
|
C | G | 1 | a0001c0001t0004g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.268-5277G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010525 | ||||||
| chr12:107010560
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268-5312G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010560 | ||||||
| chr12:107010561
|
A | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-5313T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010561 | ||||||
| chr12:107010714
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.268-5466G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010714 | ||||||
| chr12:107010788
|
GCCATGAA others(6): Show |
G | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 97 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.268-5553_268-5541d others(15): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010788 | ||||||
| chr12:107010798
|
G | A | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-5550C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010798 | ||||||
| chr12:107010968
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.268-5720A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010968 | ||||||
| chr12:107011011
|
A | G | 3 | a0001c0001t0001g0107a0001c0001t0001g0113a0001c0001t0001g0120 | 3 | HG00735.hp2 HG01070.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.268-5763T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011011 | ||||||
| chr12:107011012
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.268-5764T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011012 | ||||||
| chr12:107011085
|
G | A | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-5837C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011085 | ||||||
| chr12:107011118
|
G | A | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.268-5870C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011118 | ||||||
| chr12:107011121
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.268-5873G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011121 | ||||||
| chr12:107011214
|
G | A | 1 | a0001c0001t0002g0253 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.268-5966C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011214 | ||||||
| chr12:107011236
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.268-5988C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011236 | ||||||
| chr12:107011354
|
A | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-6106T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011354 | ||||||
| chr12:107011360
|
CA | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 256 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.268-6113delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011360 | ||||||
| chr12:107011364
|
A | C | 2 | a0001c0001t0005g0234a0001c0002t0003g0206 | 2 | HG02027.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.268-6116T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011364 | ||||||
| chr12:107011365
|
A | C | 8 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG00099.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.268-6117T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011365 | ||||||
| chr12:107011489
|
G | A | 2 | a0001c0002t0003g0182a0001c0002t0003g0183 | 2 | NA18989.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.268-6241C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011489 | ||||||
| chr12:107011668
|
T | G | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-6420A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011668 | ||||||
| chr12:107011678
|
G | C | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.268-6430C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011678 | ||||||
| chr12:107011711
|
G | A | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.268-6463C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011711 | ||||||
| chr12:107011813
|
A | G | 37 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0062others(34): Show | 38 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.268-6565T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011813 | ||||||
| chr12:107011840
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.268-6592C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011840 | ||||||
| chr12:107011898
|
A | C | 2 | a0001c0001t0005g0231a0001c0001t0005g0233 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.268-6650T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011898 | ||||||
| chr12:107012049
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.268-6801C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012049 | ||||||
| chr12:107012144
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.268-6896G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012144 | ||||||
| chr12:107012163
|
G | A | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.268-6915C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012163 | ||||||
| chr12:107012203
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.268-6955C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012203 | ||||||
| chr12:107012244
|
G | C | 3 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0155 | 4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-6996C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012244 | ||||||
| chr12:107012353
|
T | C | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-7105A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012353 | ||||||
| chr12:107012354
|
C | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-7106G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012354 | ||||||
| chr12:107012363
|
C | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.268-7115G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012363 | ||||||
| chr12:107012374
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.268-7126G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012374 | ||||||
| chr12:107012375
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.268-7127T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012375 | ||||||
| chr12:107012630
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268-7382T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012630 | ||||||
| chr12:107012710
|
A | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-7462T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012710 | ||||||
| chr12:107013038
|
C | T | 1 | a0001c0002t0003g0200 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.268-7790G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013038 | ||||||
| chr12:107013054
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.268-7806C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013054 | ||||||
| chr12:107013188
|
A | C | 1 | a0001c0001t0001g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.268-7940T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013188 | ||||||
| chr12:107013239
|
C | T | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-7991G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013239 | ||||||
| chr12:107013289
|
T | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.268-8041A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013289 | ||||||
| chr12:107013323
|
A | G | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.268-8075T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013323 | ||||||
| chr12:107013505
|
T | C | 2 | a0001c0001t0007g0023a0001c0001t0007g0024 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.268-8257A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013505 | ||||||
| chr12:107013724
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+8360G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013724 | ||||||
| chr12:107013760
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.267+8324G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013760 | ||||||
| chr12:107013796
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.267+8288C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013796 | ||||||
| chr12:107013818
|
A | G | 1 | a0001c0002t0003g0180 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.267+8266T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013818 | ||||||
| chr12:107013996
|
T | C | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+8088A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013996 | ||||||
| chr12:107014027
|
C | T | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+8057G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014027 | ||||||
| chr12:107014133
|
AC | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0018others(47): Show | 51 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.267+7950delG | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014133 | ||||||
| chr12:107014240
|
T | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.267+7844A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014240 | ||||||
| chr12:107014299
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.267+7785A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014299 | ||||||
| chr12:107014359
|
G | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+7725C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014359 | ||||||
| chr12:107014379
|
G | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.267+7705C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014379 | ||||||
| chr12:107014380
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.267+7704C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014380 | ||||||
| chr12:107014404
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.267+7680T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014404 | ||||||
| chr12:107014470
|
T | C | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.267+7614A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014470 | ||||||
| chr12:107014588
|
TACTA | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.267+7492_267+7495d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014588 | ||||||
| chr12:107014626
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.267+7458T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014626 | ||||||
| chr12:107014689
|
G | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.267+7395C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014689 | ||||||
| chr12:107014775
|
C | A | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0308 | 3 | HG02602.hp1 NA18943.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.267+7309G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014775 | ||||||
| chr12:107014919
|
G | A | 1 | a0001c0001t0002g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.267+7165C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014919 | ||||||
| chr12:107015167
|
C | T | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+6917G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015167 | ||||||
| chr12:107015206
|
C | T | 3 | a0001c0001t0002g0242a0001c0001t0002g0289a0001c0004t0002g0288 | 3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.267+6878G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015206 | ||||||
| chr12:107015344
|
CT | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 171 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.267+6739delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015344 | ||||||
| chr12:107015359
|
A | G | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+6725T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015359 | ||||||
| chr12:107015369
|
T | A | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.267+6715A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015369 | ||||||
| chr12:107015370
|
C | A | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.267+6714G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015370 | ||||||
| chr12:107015492
|
C | T | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.267+6592G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015492 | ||||||
| chr12:107015506
|
G | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+6578C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015506 | ||||||
| chr12:107015536
|
G | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+6548C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015536 | ||||||
| chr12:107015598
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG00609.hp1 NA18943.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+6486C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015598 | ||||||
| chr12:107015706
|
G | A | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+6378C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015706 | ||||||
| chr12:107015764
|
G | A | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+6320C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015764 | ||||||
| chr12:107015898
|
C | A | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.267+6186G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015898 | ||||||
| chr12:107016018
|
T | C | 2 | a0001c0003t0006g0157a0001c0003t0006g0160 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.267+6066A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016018 | ||||||
| chr12:107016045
|
C | G | 3 | a0001c0001t0002g0242a0001c0001t0002g0289a0001c0004t0002g0288 | 3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.267+6039G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016045 | ||||||
| chr12:107016110
|
G | T | 1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.267+5974C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016110 | ||||||
| chr12:107016116
|
G | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.267+5968C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016116 | ||||||
| chr12:107016126
|
A | G | 1 | a0001c0002t0003g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.267+5958T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016126 | ||||||
| chr12:107016161
|
T | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.267+5923A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016161 | ||||||
| chr12:107016274
|
C | T | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.267+5810G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016274 | ||||||
| chr12:107016324
|
A | G | 1 | a0001c0001t0004g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.267+5760T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016324 | ||||||
| chr12:107016370
|
A | T | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.267+5714T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016370 | ||||||
| chr12:107016841
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.267+5243G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016841 | ||||||
| chr12:107017053
|
C | T | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.267+5031G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017053 | ||||||
| chr12:107017082
|
G | A | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.267+5002C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017082 | ||||||
| chr12:107017156
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.267+4928G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017156 | ||||||
| chr12:107017157
|
G | A | 1 | a0001c0002t0003g0187 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.267+4927C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017157 | ||||||
| chr12:107017537
|
T | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+4547A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017537 | ||||||
| chr12:107017645
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0015g0309 | 2 | HG01243.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.267+4439G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017645 | ||||||
| chr12:107017686
|
A | G | 1 | a0001c0001t0002g0287 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.267+4398T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017686 | ||||||
| chr12:107017799
|
C | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+4285G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017799 | ||||||
| chr12:107017827
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.267+4257G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017827 | ||||||
| chr12:107018013
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.267+4071G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018013 | ||||||
| chr12:107018276
|
T | C | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.267+3808A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018276 | ||||||
| chr12:107018424
|
T | C | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+3660A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018424 | ||||||
| chr12:107018484
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.267+3600C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018484 | ||||||
| chr12:107018528
|
A | G | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+3556T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018528 | ||||||
| chr12:107018600
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.267+3484T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018600 | ||||||
| chr12:107018672
|
C | T | 13 | a0001c0001t0002g0248a0001c0001t0002g0261a0001c0001t0002g0262others(10): Show | 13 | HG01123.hp1 HG01433.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.267+3412G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018672 | ||||||
| chr12:107018731
|
A | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+3353T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018731 | ||||||
| chr12:107018752
|
A | G | 4 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0209others(1): Show | 4 | HG01361.hp2 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+3332T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018752 | ||||||
| chr12:107018859
|
G | C | 7 | a0001c0001t0002g0238a0001c0001t0002g0295a0001c0001t0002g0296others(4): Show | 7 | HG01943.hp1 NA18948.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.267+3225C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018859 | ||||||
| chr12:107019074
|
C | G | 1 | a0001c0001t0002g0266 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.267+3010G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019074 | ||||||
| chr12:107019092
|
AG | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.267+2991delC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019092 | ||||||
| chr12:107019123
|
G | T | 1 | a0001c0002t0003g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.267+2961C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019123 | ||||||
| chr12:107019216
|
CT | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.267+2867delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019216 | ||||||
| chr12:107019510
|
A | G | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.267+2574T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019510 | ||||||
| chr12:107019644
|
A | ACTAGGG | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+2434_267+2439d others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019644 | ||||||
| chr12:107019863
|
G | A | 1 | a0001c0001t0004g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.267+2221C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019863 | ||||||
| chr12:107019910
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.267+2174G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019910 | ||||||
| chr12:107020186
|
C | CA | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 246 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.267+1897dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020186 | ||||||
| chr12:107020186
|
C | CAA | 15 | a0001c0001t0001g0116a0001c0001t0002g0238a0001c0001t0002g0257others(12): Show | 15 | HG01943.hp1 HG02300.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.267+1896_267+1897d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020186 | ||||||
| chr12:107020229
|
G | C | 2 | a0001c0002t0003g0189a0001c0002t0003g0222 | 2 | HG02145.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.267+1855C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020229 | ||||||
| chr12:107020316
|
T | C | 1 | a0001c0002t0003g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.267+1768A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020316 | ||||||
| chr12:107020381
|
T | C | 1 | a0001c0002t0003g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.267+1703A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020381 | ||||||
| chr12:107020395
|
T | C | 1 | a0001c0002t0003g0186 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.267+1689A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020395 | ||||||
| chr12:107020471
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.267+1613A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020471 | ||||||
| chr12:107020525
|
G | GT | 80 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(77): Show | 82 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.267+1558dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020525 | ||||||
| chr12:107020525
|
GT | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 180 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.267+1558delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020525 | ||||||
| chr12:107020565
|
C | T | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.267+1519G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020565 | ||||||
| chr12:107020681
|
C | T | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+1403G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020681 | ||||||
| chr12:107020687
|
G | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.267+1397C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020687 | ||||||
| chr12:107021096
|
C | G | 1 | a0001c0001t0003g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.267+988G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021096 | ||||||
| chr12:107021152
|
G | A | 2 | a0001c0003t0006g0157a0001c0003t0006g0160 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.267+932C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021152 | ||||||
| chr12:107021156
|
G | A | 3 | a0001c0001t0002g0242a0001c0001t0002g0289a0001c0004t0002g0288 | 3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.267+928C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021156 | ||||||
| chr12:107021228
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.267+856G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021228 | ||||||
| chr12:107021261
|
C | T | 76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.267+823G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021261 | ||||||
| chr12:107021295
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.267+789T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021295 | ||||||
| chr12:107021350
|
T | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02630.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+734A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021350 | ||||||
| chr12:107021352
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.267+732C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021352 | ||||||
| chr12:107021379
|
C | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.267+705G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021379 | ||||||
| chr12:107021386
|
T | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.267+698A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021386 | ||||||
| chr12:107021460
|
C | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.267+624G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021460 | ||||||
| chr12:107021525
|
T | C | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+559A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021525 | ||||||
| chr12:107021657
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.267+427G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021657 | ||||||
| chr12:107021663
|
C | T | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+421G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021663 | ||||||
| chr12:107021701
|
CAT | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0041a0001c0001t0001g0046others(3): Show | 6 | HG00609.hp1 HG02132.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+381_267+382del others(2): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021701 | ||||||
| chr12:107021725
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.267+359G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021725 | ||||||
| chr12:107021729
|
A | T | 1 | a0001c0002t0003g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.267+355T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021729 | ||||||
| chr12:107021741
|
T | C | 76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.267+343A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021741 | ||||||
| chr12:107021749
|
C | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.267+335G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021749 | ||||||
| chr12:107021772
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.267+312C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021772 | ||||||
| chr12:107021815
|
T | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.267+269A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021815 | ||||||
| chr12:107021878
|
T | C | 3 | a0001c0001t0002g0239a0001c0001t0002g0265a0001c0001t0002g0306 | 3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.267+206A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021878 | ||||||
| chr12:107022373
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.159-181T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022373 | ||||||
| chr12:107022470
|
A | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0153 | 3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.159-278T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022470 | ||||||
| chr12:107022493
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-301A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022493 | ||||||
| chr12:107022553
|
A | G | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-361T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022553 | ||||||
| chr12:107022770
|
AAAAG | A | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-582_159-579del others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022770 | ||||||
| chr12:107022813
|
T | C | 3 | a0001c0001t0002g0242a0001c0001t0002g0289a0001c0004t0002g0288 | 3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.159-621A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022813 | ||||||
| chr12:107022845
|
TA | T | 81 | a0001c0001t0001g0012a0001c0001t0001g0135a0001c0001t0002g0009others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-654delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022845 | ||||||
| chr12:107022999
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.159-807C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022999 | ||||||
| chr12:107023063
|
ATTAT | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-875_159-872del others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023063 | ||||||
| chr12:107023149
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-957A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023149 | ||||||
| chr12:107023270
|
G | A | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-1078C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023270 | ||||||
| chr12:107023287
|
G | T | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-1095C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023287 | ||||||
| chr12:107023404
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159-1212C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023404 | ||||||
| chr12:107023588
|
G | A | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-1396C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023588 | ||||||
| chr12:107023866
|
G | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-1674C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023866 | ||||||
| chr12:107023945
|
T | A | 1 | a0001c0001t0002g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159-1753A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023945 | ||||||
| chr12:107024013
|
C | G | 1 | a0001c0001t0002g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.159-1821G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024013 | ||||||
| chr12:107024300
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.159-2108G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024300 | ||||||
| chr12:107024699
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.159-2507G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024699 | ||||||
| chr12:107024721
|
T | A | 3 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0155 | 4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-2529A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024721 | ||||||
| chr12:107024848
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-2656G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024848 | ||||||
| chr12:107024885
|
T | TA | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-2694dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024885 | ||||||
| chr12:107025036
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-2844A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025036 | ||||||
| chr12:107025193
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.159-3001G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025193 | ||||||
| chr12:107025266
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0011g0245 | 3 | HG00140.hp2 HG01261.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.159-3074G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025266 | ||||||
| chr12:107025274
|
A | T | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-3082T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025274 | ||||||
| chr12:107025282
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.159-3090A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025282 | ||||||
| chr12:107025479
|
G | A | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-3287C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025479 | ||||||
| chr12:107025807
|
T | G | 1 | a0001c0002t0003g0008 | 2 | NA18975.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.159-3615A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025807 | ||||||
| chr12:107025884
|
C | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-3692G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025884 | ||||||
| chr12:107026111
|
AAT | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 6 | HG00735.hp2 HG01070.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-3921_159-3920d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026111 | ||||||
| chr12:107026134
|
C | CATATAAT others(34): Show |
1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159-3943_159-3942i others(43): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | ||||||
| chr12:107026134
|
C | CATATATA others(204): Show |
1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-3943_159-3942i others(213): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | ||||||
| chr12:107026134
|
C | CATATATA others(88): Show |
4 | a0001c0001t0004g0164a0001c0001t0004g0165a0001c0001t0004g0166others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3943_159-3942i others(97): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | ||||||
| chr12:107026134
|
C | CATATATA others(118): Show |
4 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0168others(1): Show | 5 | HG01884.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-3943_159-3942i others(127): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | ||||||
| chr12:107026134
|
C | CATATATA others(146): Show |
2 | a0001c0001t0004g0162a0001c0001t0004g0163 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.159-3943_159-3942i others(155): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | ||||||
| chr12:107026134
|
C | CATATATA others(25): Show |
1 | a0001c0002t0003g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-3974_159-3943d others(34): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | ||||||
| chr12:107026134
|
C | CATATATG others(155): Show |
2 | a0001c0001t0004g0006a0001c0001t0004g0153 | 3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.159-3943_159-3942i others(164): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | ||||||
| chr12:107026134
|
C | CATATATG others(155): Show |
1 | a0001c0001t0004g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.159-3943_159-3942i others(164): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | ||||||
| chr12:107026143
|
T | TACATATA others(152): Show |
1 | a0001c0001t0004g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.159-3952_159-3951i others(161): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026143 | ||||||
| chr12:107026147
|
T | TAAATAAC others(60): Show |
1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(69): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(64): Show |
7 | a0001c0001t0001g0046a0001c0001t0001g0093a0001c0001t0001g0098others(4): Show | 7 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(73): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(145): Show |
1 | a0001c0001t0002g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159-3956_159-3955i others(154): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(62): Show |
103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 106 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(71): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(92): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0027others(19): Show | 23 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(101): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(122): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0144 | 2 | HG01261.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.159-3956_159-3955i others(131): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(60): Show |
12 | a0001c0001t0001g0036a0001c0001t0001g0145a0001c0001t0001g0146others(9): Show | 12 | HG02109.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(69): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(88): Show |
2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-3956_159-3955i others(97): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(328): Show |
1 | a0001c0001t0002g0271 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(337): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(120): Show |
36 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(33): Show | 38 | HG00558.hp2 HG01175.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(129): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(150): Show |
17 | a0001c0001t0002g0239a0001c0001t0002g0241a0001c0001t0002g0242others(14): Show | 17 | HG00673.hp1 HG01978.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(159): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(180): Show |
11 | a0001c0001t0002g0248a0001c0001t0002g0261a0001c0001t0002g0263others(8): Show | 11 | HG00558.hp1 HG01123.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(189): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(300): Show |
1 | a0001c0001t0002g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(309): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(330): Show |
1 | a0001c0001t0002g0270 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(339): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(150): Show |
1 | a0001c0001t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159-3956_159-3955i others(159): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(178): Show |
1 | a0001c0001t0002g0265 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.159-3956_159-3955i others(187): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(206): Show |
1 | a0001c0001t0002g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.159-3956_159-3955i others(215): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(146): Show |
1 | a0001c0001t0002g0244 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(155): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(147): Show |
2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.159-3956_159-3955i others(156): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026147
|
T | TATATAAC others(148): Show |
1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(157): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | ||||||
| chr12:107026149
|
T | TATAAC | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3958_159-3957i others(7): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026149 | ||||||
| chr12:107026149
|
T | TATAACAT others(118): Show |
1 | a0001c0001t0002g0255 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.159-3958_159-3957i others(127): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026149 | ||||||
| chr12:107026149
|
T | TATAACAT others(49): Show |
3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-3958_159-3957i others(58): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026149 | ||||||
| chr12:107026152
|
A | AACATATA others(64): Show |
1 | a0001c0001t0001g0001 | 3 | HG01516.hp1 HG06807.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.159-3961_159-3960i others(73): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026152 | ||||||
| chr12:107026157
|
A | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 234 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.159-3965T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026157 | ||||||
| chr12:107026158
|
A | C | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3966T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026158 | ||||||
| chr12:107026158
|
AAT | A | 2 | a0001c0001t0001g0001a0001c0001t0015g0309 | 4 | HG01243.hp2 HG01516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-3968_159-3967d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026158 | ||||||
| chr12:107026160
|
T | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 234 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.159-3968A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026160 | ||||||
| chr12:107026160
|
T | TATATATA others(21): Show |
1 | a0001c0002t0003g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.159-3969_159-3968i others(30): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026160 | ||||||
| chr12:107026162
|
T | TATATGTT others(53): Show |
4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3971_159-3970i others(62): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026162 | ||||||
| chr12:107026164
|
T | A | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-3972A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026164 | ||||||
| chr12:107026183
|
T | C | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-3991A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026183 | ||||||
| chr12:107026295
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0126 | 2 | NA19011.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.159-4103C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026295 | ||||||
| chr12:107026404
|
T | C | 1 | a0001c0001t0008g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.159-4212A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026404 | ||||||
| chr12:107026430
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.159-4238G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026430 | ||||||
| chr12:107026643
|
T | C | 1 | a0001c0001t0002g0294 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.159-4451A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026643 | ||||||
| chr12:107026667
|
T | C | 3 | a0001c0002t0003g0190a0001c0002t0003g0206a0001c0002t0003g0213 | 3 | HG02027.hp1 NA18963.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.159-4475A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026667 | ||||||
| chr12:107026769
|
G | GT | 15 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(12): Show | 15 | HG00140.hp1 HG01074.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.159-4578dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | ||||||
| chr12:107026769
|
GT | G | 62 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(59): Show | 64 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.159-4578delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | ||||||
| chr12:107026769
|
GTT | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0055others(22): Show | 27 | HG01516.hp1 HG01943.hp1 HG02027.hp2 others(24): Show |
intron_variant | MODIFIER | c.159-4579_159-4578d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | ||||||
| chr12:107026769
|
GTTT | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 149 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.159-4580_159-4578d others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | ||||||
| chr12:107026769
|
GTTTT | G | 12 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(9): Show | 12 | HG01167.hp1 HG01167.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-4581_159-4578d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | ||||||
| chr12:107027477
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.159-5285T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107027477 | ||||||
| chr12:107027483
|
T | A | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-5291A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107027483 | ||||||
| chr12:107028500
|
C | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-6308G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107028500 | ||||||
| chr12:107028552
|
A | T | 1 | a0001c0001t0002g0256 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.159-6360T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107028552 | ||||||
| chr12:107028803
|
T | C | 1 | a0001c0002t0003g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.159-6611A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107028803 | ||||||
| chr12:107029179
|
G | GTGCA | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-6991_159-6988d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029179 | ||||||
| chr12:107029402
|
A | G | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-7210T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029402 | ||||||
| chr12:107029428
|
C | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0155 | 4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-7236G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029428 | ||||||
| chr12:107029451
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-7259C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029451 | ||||||
| chr12:107029497
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159-7305C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029497 | ||||||
| chr12:107029538
|
C | A | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-7346G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029538 | ||||||
| chr12:107029606
|
C | CA | 77 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(74): Show | 79 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.159-7415dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029606 | ||||||
| chr12:107029606
|
CA | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.159-7415delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029606 | ||||||
| chr12:107029637
|
T | A | 3 | a0001c0002t0003g0198a0001c0002t0003g0201a0001c0002t0003g0202 | 3 | HG01070.hp2 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.159-7445A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029637 | ||||||
| chr12:107029677
|
T | G | 1 | a0001c0001t0002g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.159-7485A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029677 | ||||||
| chr12:107029799
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.159-7607T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029799 | ||||||
| chr12:107030205
|
A | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-8013T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107030205 | ||||||
| chr12:107030331
|
C | A | 1 | a0001c0002t0003g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.159-8139G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107030331 | ||||||
| chr12:107030952
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.159-8760C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107030952 | ||||||
| chr12:107031029
|
A | C | 3 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0283 | 3 | HG02109.hp2 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.159-8837T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031029 | ||||||
| chr12:107031115
|
A | AAAC | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-8926_159-8924d others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031115 | ||||||
| chr12:107031223
|
T | C | 1 | a0001c0001t0002g0254 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.159-9031A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031223 | ||||||
| chr12:107031338
|
C | A | 1 | a0001c0002t0003g0213 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.159-9146G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031338 | ||||||
| chr12:107031370
|
C | CT | 9 | a0001c0001t0001g0035a0001c0001t0001g0118a0001c0001t0001g0125others(6): Show | 9 | HG01074.hp2 HG01256.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.159-9179dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031370 | ||||||
| chr12:107031416
|
T | C | 1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159-9224A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031416 | ||||||
| chr12:107031801
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159-9609A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031801 | ||||||
| chr12:107031860
|
T | C | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-9668A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031860 | ||||||
| chr12:107031948
|
T | G | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-9756A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031948 | ||||||
| chr12:107031991
|
G | C | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-9799C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031991 | ||||||
| chr12:107032046
|
T | C | 1 | a0001c0002t0003g0217 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.159-9854A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032046 | ||||||
| chr12:107032123
|
G | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-9931C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032123 | ||||||
| chr12:107032373
|
A | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-10181T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032373 | ||||||
| chr12:107032394
|
G | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-10202C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032394 | ||||||
| chr12:107032490
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159-10298G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032490 | ||||||
| chr12:107032505
|
T | TACAA | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | NA18612.hp1 NA18947.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.159-10314_159-1031 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032505 | ||||||
| chr12:107032507
|
C | CAA | 46 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 47 | HG00597.hp1 HG00673.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.159-10316_159-1031 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032507 | ||||||
| chr12:107032509
|
G | C | 51 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(48): Show | 52 | HG00597.hp1 HG00673.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.159-10317C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032509 | ||||||
| chr12:107032509
|
G | GAC | 56 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.159-10319_159-1031 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032509 | ||||||
| chr12:107032509
|
G | GACAC | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0026others(36): Show | 42 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.159-10321_159-1031 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032509 | ||||||
| chr12:107032509
|
G | GACACAC | 7 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 8 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.159-10323_159-1031 others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032509 | ||||||
| chr12:107032584
|
C | T | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-10392G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032584 | ||||||
| chr12:107032826
|
T | A | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-10634A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032826 | ||||||
| chr12:107033003
|
C | T | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-10811G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033003 | ||||||
| chr12:107033264
|
T | G | 3 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0155 | 4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-11072A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033264 | ||||||
| chr12:107033353
|
A | C | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02257.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-11161T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033353 | ||||||
| chr12:107033376
|
G | A | 8 | a0001c0001t0002g0241a0001c0001t0002g0243a0001c0001t0002g0273others(5): Show | 8 | HG02559.hp2 HG02735.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.159-11184C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033376 | ||||||
| chr12:107033724
|
T | C | 2 | a0001c0001t0007g0023a0001c0001t0007g0024 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159-11532A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033724 | ||||||
| chr12:107033770
|
G | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.159-11578C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033770 | ||||||
| chr12:107033932
|
G | C | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-11740C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033932 | ||||||
| chr12:107034136
|
G | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 260 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.159-11944C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034136 | ||||||
| chr12:107034261
|
C | T | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-12069G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034261 | ||||||
| chr12:107034312
|
G | C | 1 | a0001c0001t0002g0296 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.159-12120C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034312 | ||||||
| chr12:107034349
|
G | A | 1 | a0001c0002t0003g0223 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.159-12157C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034349 | ||||||
| chr12:107034508
|
C | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-12316G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034508 | ||||||
| chr12:107034609
|
C | A | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-12417G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034609 | ||||||
| chr12:107034633
|
T | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02630.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-12441A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034633 | ||||||
| chr12:107034781
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.159-12589T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034781 | ||||||
| chr12:107035138
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.159-12946T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035138 | ||||||
| chr12:107035263
|
T | G | 1 | a0001c0001t0002g0254 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.159-13071A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035263 | ||||||
| chr12:107035345
|
C | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0064 | 3 | HG02683.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.159-13153G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035345 | ||||||
| chr12:107035376
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.159-13184A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035376 | ||||||
| chr12:107035823
|
T | C | 8 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(5): Show | 9 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.159-13631A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035823 | ||||||
| chr12:107036004
|
A | G | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-13812T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036004 | ||||||
| chr12:107036102
|
T | C | 1 | a0001c0001t0002g0276 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.159-13910A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036102 | ||||||
| chr12:107036128
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0126 | 2 | NA19011.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.159-13936C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036128 | ||||||
| chr12:107036137
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.159-13945A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036137 | ||||||
| chr12:107036274
|
T | C | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-14082A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036274 | ||||||
| chr12:107036583
|
TGG | T | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-14393_159-1439 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036583 | ||||||
| chr12:107036585
|
G | GT | 10 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0048others(7): Show | 11 | HG01261.hp2 HG03209.hp2 HG04184.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-14394dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036585 | ||||||
| chr12:107036585
|
GT | G | 70 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(67): Show | 72 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.159-14394delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036585 | ||||||
| chr12:107036736
|
A | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-14544T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036736 | ||||||
| chr12:107036761
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.159-14569T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036761 | ||||||
| chr12:107036913
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-14721G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036913 | ||||||
| chr12:107036972
|
T | C | 76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.159-14780A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036972 | ||||||
| chr12:107037178
|
G | A | 2 | a0001c0002t0003g0201a0001c0002t0003g0202 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.159-14986C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037178 | ||||||
| chr12:107037446
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.159-15254G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037446 | ||||||
| chr12:107037658
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-15466C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037658 | ||||||
| chr12:107037697
|
TTTTA | T | 87 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(84): Show | 89 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.159-15509_159-1550 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037697 | ||||||
| chr12:107037766
|
T | A | 1 | a0001c0002t0003g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.159-15574A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037766 | ||||||
| chr12:107037911
|
G | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-15719C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037911 | ||||||
| chr12:107038034
|
T | C | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-15842A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038034 | ||||||
| chr12:107038255
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.159-16063A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038255 | ||||||
| chr12:107038284
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-16092G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038284 | ||||||
| chr12:107038378
|
G | A | 2 | a0001c0001t0002g0247a0001c0001t0002g0269 | 2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.159-16186C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038378 | ||||||
| chr12:107038403
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.159-16211T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038403 | ||||||
| chr12:107038712
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02257.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-16520G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038712 | ||||||
| chr12:107039076
|
G | A | 2 | a0001c0002t0003g0228a0001c0002t0003g0229 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.159-16884C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039076 | ||||||
| chr12:107039080
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.159-16888C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039080 | ||||||
| chr12:107039159
|
T | C | 1 | a0001c0001t0007g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.159-16967A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039159 | ||||||
| chr12:107039380
|
A | C | 3 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024 | 3 | HG02818.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159-17188T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039380 | ||||||
| chr12:107039559
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.159-17367A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039559 | ||||||
| chr12:107039606
|
A | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-17414T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039606 | ||||||
| chr12:107039644
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.159-17452C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039644 | ||||||
| chr12:107039796
|
C | T | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-17604G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039796 | ||||||
| chr12:107039894
|
C | T | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-17702G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039894 | ||||||
| chr12:107040089
|
G | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-17897C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040089 | ||||||
| chr12:107040254
|
G | C | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-18062C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040254 | ||||||
| chr12:107040271
|
CT | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.159-18080delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040271 | ||||||
| chr12:107040285
|
T | A | 7 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0061others(4): Show | 7 | HG01081.hp1 HG02135.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-18093A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040285 | ||||||
| chr12:107040286
|
A | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0061others(4): Show | 7 | HG01081.hp1 HG02135.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-18094T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040286 | ||||||
| chr12:107040287
|
G | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0061others(4): Show | 7 | HG01081.hp1 HG02135.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-18095C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040287 | ||||||
| chr12:107040287
|
GT | G | 87 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(84): Show | 89 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.159-18096delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040287 | ||||||
| chr12:107040287
|
GTT | G | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(11): Show | 16 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.159-18097_159-1809 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040287 | ||||||
| chr12:107040309
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-18117C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040309 | ||||||
| chr12:107040316
|
C | T | 2 | a0001c0001t0005g0231a0001c0001t0005g0233 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.159-18124G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040316 | ||||||
| chr12:107040336
|
AG | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.159-18145delC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040336 | ||||||
| chr12:107040393
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-18201A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040393 | ||||||
| chr12:107040411
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-18219C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040411 | ||||||
| chr12:107040646
|
T | C | 1 | a0001c0001t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159-18454A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040646 | ||||||
| chr12:107040783
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.159-18591A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040783 | ||||||
| chr12:107040873
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.159-18681C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040873 | ||||||
| chr12:107040919
|
T | TA | 9 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(6): Show | 10 | HG01167.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.159-18728dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040919 | ||||||
| chr12:107040926
|
A | G | 2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.159-18734T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040926 | ||||||
| chr12:107040941
|
G | GA | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-18750dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040941 | ||||||
| chr12:107040990
|
T | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-18798A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040990 | ||||||
| chr12:107041093
|
C | A | 1 | a0001c0002t0003g0195 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.159-18901G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041093 | ||||||
| chr12:107041121
|
G | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG01167.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.159-18929C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041121 | ||||||
| chr12:107041191
|
C | T | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-18999G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041191 | ||||||
| chr12:107041240
|
C | T | 1 | a0001c0002t0003g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-19048G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041240 | ||||||
| chr12:107041594
|
A | G | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-19402T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041594 | ||||||
| chr12:107041621
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159-19429A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041621 | ||||||
| chr12:107041627
|
A | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 260 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.159-19435T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041627 | ||||||
| chr12:107041772
|
A | G | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-19580T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041772 | ||||||
| chr12:107041773
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.159-19581A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041773 | ||||||
| chr12:107041923
|
G | A | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-19731C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041923 | ||||||
| chr12:107041930
|
C | T | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-19738G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041930 | ||||||
| chr12:107042218
|
A | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-20026T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042218 | ||||||
| chr12:107042229
|
C | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-20037G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042229 | ||||||
| chr12:107042247
|
T | C | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-20055A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042247 | ||||||
| chr12:107042408
|
C | T | 1 | a0001c0001t0002g0259 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.159-20216G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042408 | ||||||
| chr12:107042498
|
T | C | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-20306A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042498 | ||||||
| chr12:107042556
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.159-20364A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042556 | ||||||
| chr12:107042561
|
G | A | 6 | a0001c0001t0004g0156a0001c0001t0004g0164a0001c0001t0004g0165others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-20369C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042561 | ||||||
| chr12:107042571
|
C | T | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-20379G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042571 | ||||||
| chr12:107042596
|
T | C | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-20404A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042596 | ||||||
| chr12:107042607
|
AG | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-20416delC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042607 | ||||||
| chr12:107043028
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-20836G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043028 | ||||||
| chr12:107043049
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0113 | 3 | HG00735.hp2 HG01070.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.159-20857C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043049 | ||||||
| chr12:107043070
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.159-20878A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043070 | ||||||
| chr12:107043075
|
C | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00597.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.159-20883G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043075 | ||||||
| chr12:107043233
|
T | A | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-21041A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043233 | ||||||
| chr12:107043483
|
C | T | 1 | a0001c0002t0003g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.159-21291G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043483 | ||||||
| chr12:107043644
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.159-21452A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043644 | ||||||
| chr12:107043647
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.159-21455G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043647 | ||||||
| chr12:107043818
|
G | A | 2 | a0001c0002t0003g0008a0001c0002t0003g0223 | 3 | NA18975.hp2 NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.159-21626C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043818 | ||||||
| chr12:107043834
|
TAC | T | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-21644_159-2164 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043834 | ||||||
| chr12:107044289
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.159-22097C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044289 | ||||||
| chr12:107044300
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.159-22108T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044300 | ||||||
| chr12:107044359
|
C | T | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-22167G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044359 | ||||||
| chr12:107044396
|
C | A | 1 | a0001c0001t0001g0054 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.159-22204G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044396 | ||||||
| chr12:107044603
|
A | G | 1 | a0001c0002t0003g0217 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.159-22411T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044603 | ||||||
| chr12:107044793
|
A | G | 2 | a0001c0002t0003g0199a0001c0002t0003g0208 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.159-22601T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044793 | ||||||
| chr12:107044856
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-22664G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044856 | ||||||
| chr12:107045248
|
T | A | 5 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(2): Show | 6 | HG01243.hp2 HG02280.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-23056A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045248 | ||||||
| chr12:107045381
|
C | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-23189G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045381 | ||||||
| chr12:107045441
|
T | G | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-23249A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045441 | ||||||
| chr12:107045475
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.159-23283A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045475 | ||||||
| chr12:107045544
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0113 | 3 | HG00735.hp2 HG01070.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.159-23352C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045544 | ||||||
| chr12:107045582
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01361.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.159-23390G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045582 | ||||||
| chr12:107045583
|
G | A | 6 | a0001c0001t0002g0240a0001c0001t0002g0249a0001c0001t0002g0256others(3): Show | 6 | HG00673.hp1 HG01978.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-23391C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045583 | ||||||
| chr12:107045688
|
G | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-23496C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045688 | ||||||
| chr12:107045705
|
C | T | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-23513G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045705 | ||||||
| chr12:107045740
|
T | G | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-23548A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045740 | ||||||
| chr12:107045753
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.159-23561C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045753 | ||||||
| chr12:107045756
|
C | A | 1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159-23564G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045756 | ||||||
| chr12:107045768
|
T | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-23576A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045768 | ||||||
| chr12:107045823
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159-23631G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045823 | ||||||
| chr12:107045882
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.159-23690G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045882 | ||||||
| chr12:107045985
|
G | C | 1 | a0001c0002t0003g0186 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.159-23793C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045985 | ||||||
| chr12:107046125
|
TA | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.159-23934delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046125 | ||||||
| chr12:107046292
|
CA | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 180 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.159-24101delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046292 | ||||||
| chr12:107046352
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG01167.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.159-24160A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046352 | ||||||
| chr12:107046367
|
C | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159-24175G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046367 | ||||||
| chr12:107046525
|
C | T | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-24333G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046525 | ||||||
| chr12:107046644
|
C | T | 3 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024 | 3 | HG02818.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159-24452G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046644 | ||||||
| chr12:107046675
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.159-24483T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046675 | ||||||
| chr12:107046820
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.159-24628A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046820 | ||||||
| chr12:107047046
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.159-24854G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047046 | ||||||
| chr12:107047085
|
T | C | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-24893A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047085 | ||||||
| chr12:107047129
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.159-24937T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047129 | ||||||
| chr12:107047156
|
A | C | 3 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0013g0171 | 4 | HG01884.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-24964T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047156 | ||||||
| chr12:107047576
|
T | C | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-25384A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047576 | ||||||
| chr12:107047583
|
A | G | 1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.159-25391T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047583 | ||||||
| chr12:107047683
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.159-25491A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047683 | ||||||
| chr12:107047764
|
A | C | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-25572T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047764 | ||||||
| chr12:107047768
|
C | T | 1 | a0001c0001t0002g0294 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.159-25576G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047768 | ||||||
| chr12:107047774
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.159-25582T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047774 | ||||||
| chr12:107048087
|
A | AT | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-25896dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048087 | ||||||
| chr12:107048169
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.159-25977G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048169 | ||||||
| chr12:107048326
|
C | A | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-26134G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048326 | ||||||
| chr12:107048355
|
C | T | 1 | a0001c0002t0012g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.159-26163G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048355 | ||||||
| chr12:107048364
|
G | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-26172C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048364 | ||||||
| chr12:107048425
|
A | T | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-26233T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048425 | ||||||
| chr12:107048505
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-26313A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048505 | ||||||
| chr12:107048537
|
C | T | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-26345G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048537 | ||||||
| chr12:107048878
|
C | T | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-26686G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048878 | ||||||
| chr12:107048982
|
A | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-26790T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048982 | ||||||
| chr12:107049237
|
A | G | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-27045T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049237 | ||||||
| chr12:107049521
|
C | T | 2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159-27329G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049521 | ||||||
| chr12:107049589
|
C | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-27397G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049589 | ||||||
| chr12:107049629
|
C | T | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-27437G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049629 | ||||||
| chr12:107049676
|
A | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-27484T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049676 | ||||||
| chr12:107049762
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-27570A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049762 | ||||||
| chr12:107049768
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.159-27576A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049768 | ||||||
| chr12:107049997
|
G | A | 1 | a0001c0001t0004g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.159-27805C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049997 | ||||||
| chr12:107050374
|
G | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-28182C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050374 | ||||||
| chr12:107050375
|
G | C | 1 | a0001c0001t0010g0045 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.159-28183C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050375 | ||||||
| chr12:107050428
|
C | T | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-28236G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050428 | ||||||
| chr12:107050443
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.159-28251C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050443 | ||||||
| chr12:107050449
|
A | G | 1 | a0001c0001t0004g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.159-28257T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050449 | ||||||
| chr12:107050488
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.159-28296G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050488 | ||||||
| chr12:107050805
|
C | T | 6 | a0001c0002t0003g0180a0001c0002t0003g0181a0001c0002t0003g0189others(3): Show | 6 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-28613G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050805 | ||||||
| chr12:107050897
|
G | C | 2 | a0001c0002t0003g0203a0001c0002t0003g0216 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.159-28705C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050897 | ||||||
| chr12:107050943
|
G | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0027others(15): Show | 19 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.159-28751C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050943 | ||||||
| chr12:107051050
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.159-28858C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051050 | ||||||
| chr12:107051317
|
T | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159-29125A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051317 | ||||||
| chr12:107051359
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.159-29167A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051359 | ||||||
| chr12:107051882
|
C | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 179 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.159-29690G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051882 | ||||||
| chr12:107051952
|
A | ATTGTC | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-29761_159-2976 others(9): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051952 | ||||||
| chr12:107052103
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.159-29911C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052103 | ||||||
| chr12:107052183
|
ATACCCAG others(2): Show |
A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(90): Show | 98 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.159-30000_159-2999 others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052183 | ||||||
| chr12:107052199
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(90): Show | 98 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.159-30007T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052199 | ||||||
| chr12:107052250
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.159-30058T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052250 | ||||||
| chr12:107052641
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.159-30449A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052641 | ||||||
| chr12:107052804
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.159-30612A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052804 | ||||||
| chr12:107052828
|
G | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG00639.hp1 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-30636C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052828 | ||||||
| chr12:107053063
|
C | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-30871G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053063 | ||||||
| chr12:107053129
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.159-30937C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053129 | ||||||
| chr12:107053214
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0063 | 4 | HG01516.hp1 HG04199.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-31022A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053214 | ||||||
| chr12:107053333
|
T | C | 6 | a0001c0001t0004g0156a0001c0001t0004g0164a0001c0001t0004g0165others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-31141A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053333 | ||||||
| chr12:107053387
|
G | T | 6 | a0001c0001t0004g0156a0001c0001t0004g0164a0001c0001t0004g0165others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-31195C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053387 | ||||||
| chr12:107053446
|
A | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-31254T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053446 | ||||||
| chr12:107053561
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.159-31369C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053561 | ||||||
| chr12:107053573
|
C | T | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-31381G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053573 | ||||||
| chr12:107053691
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.159-31499A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053691 | ||||||
| chr12:107053864
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01256.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.159-31672T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053864 | ||||||
| chr12:107053964
|
G | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-31772C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053964 | ||||||
| chr12:107054555
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 232 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.159-32363G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054555 | ||||||
| chr12:107054587
|
C | T | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-32395G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054587 | ||||||
| chr12:107054650
|
G | GA | 12 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0146others(9): Show | 12 | HG02257.hp2 HG02602.hp1 HG04228.hp2 others(9): Show |
intron_variant | MODIFIER | c.159-32459dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054650 | ||||||
| chr12:107054663
|
A | G | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-32471T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054663 | ||||||
| chr12:107054763
|
C | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-32571G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054763 | ||||||
| chr12:107054845
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-32653C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054845 | ||||||
| chr12:107055213
|
T | C | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-33021A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055213 | ||||||
| chr12:107055401
|
T | C | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | NA18949.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.159-33209A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055401 | ||||||
| chr12:107055634
|
T | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02630.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-33442A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055634 | ||||||
| chr12:107055639
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.159-33447A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055639 | ||||||
| chr12:107055972
|
T | C | 2 | a0001c0001t0007g0023a0001c0001t0007g0024 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159-33780A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055972 | ||||||
| chr12:107056049
|
G | A | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-33857C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056049 | ||||||
| chr12:107056336
|
G | C | 9 | a0001c0001t0002g0248a0001c0001t0002g0261a0001c0001t0002g0262others(6): Show | 9 | HG01123.hp1 HG01433.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.159-34144C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056336 | ||||||
| chr12:107056400
|
A | G | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-34208T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056400 | ||||||
| chr12:107056415
|
C | G | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-34223G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056415 | ||||||
| chr12:107056580
|
C | CT | 76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.159-34389dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056580 | ||||||
| chr12:107056606
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.159-34414T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056606 | ||||||
| chr12:107056689
|
G | A | 1 | a0001c0002t0003g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.159-34497C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056689 | ||||||
| chr12:107056974
|
T | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.159-34782A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056974 | ||||||
| chr12:107057088
|
A | C | 1 | a0001c0001t0002g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.159-34896T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057088 | ||||||
| chr12:107057096
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.159-34904C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057096 | ||||||
| chr12:107057220
|
A | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-35028T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057220 | ||||||
| chr12:107057456
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.159-35264A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057456 | ||||||
| chr12:107057495
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-35303G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057495 | ||||||
| chr12:107057592
|
G | A | 1 | a0001c0002t0003g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.158+35212C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057592 | ||||||
| chr12:107057722
|
C | G | 1 | a0001c0002t0003g0175 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.158+35082G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057722 | ||||||
| chr12:107057875
|
A | T | 1 | a0001c0002t0003g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.158+34929T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057875 | ||||||
| chr12:107058292
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+34512T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058292 | ||||||
| chr12:107058309
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.158+34495G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058309 | ||||||
| chr12:107058359
|
A | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+34445T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058359 | ||||||
| chr12:107058538
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+34266C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058538 | ||||||
| chr12:107058685
|
T | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+34119A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058685 | ||||||
| chr12:107058717
|
G | A | 1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.158+34087C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058717 | ||||||
| chr12:107059007
|
C | T | 35 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0093others(32): Show | 36 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.158+33797G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059007 | ||||||
| chr12:107059248
|
T | C | 3 | a0001c0001t0002g0239a0001c0001t0002g0265a0001c0001t0002g0306 | 3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.158+33556A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059248 | ||||||
| chr12:107059254
|
TTTTG | T | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+33546_158+3354 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059254 | ||||||
| chr12:107059261
|
T | C | 3 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0308 | 3 | HG02602.hp1 NA18943.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.158+33543A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059261 | ||||||
| chr12:107059272
|
AACAGGGT others(8): Show |
A | 1 | a0001c0001t0001g0144 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+33517_158+3353 others(19): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059272 | ||||||
| chr12:107059278
|
G | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+33526C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059278 | ||||||
| chr12:107059578
|
G | A | 2 | a0001c0001t0002g0247a0001c0001t0002g0269 | 2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.158+33226C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059578 | ||||||
| chr12:107060078
|
A | T | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 81 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.158+32726T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060078 | ||||||
| chr12:107060079
|
T | G | 83 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(80): Show | 86 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.158+32725A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060079 | ||||||
| chr12:107060081
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.158+32723G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060081 | ||||||
| chr12:107060082
|
G | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 81 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.158+32722C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060082 | ||||||
| chr12:107060196
|
T | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+32608A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060196 | ||||||
| chr12:107060282
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.158+32522C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060282 | ||||||
| chr12:107060343
|
C | T | 3 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0209 | 3 | HG01361.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.158+32461G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060343 | ||||||
| chr12:107060374
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.158+32430A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060374 | ||||||
| chr12:107060488
|
T | C | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+32316A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060488 | ||||||
| chr12:107060519
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.158+32285A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060519 | ||||||
| chr12:107060712
|
C | T | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+32092G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060712 | ||||||
| chr12:107060737
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+32067A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060737 | ||||||
| chr12:107060997
|
A | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+31807T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060997 | ||||||
| chr12:107061005
|
T | G | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+31799A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061005 | ||||||
| chr12:107061307
|
A | G | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+31497T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061307 | ||||||
| chr12:107061311
|
C | G | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+31493G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061311 | ||||||
| chr12:107061318
|
A | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+31486T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061318 | ||||||
| chr12:107061363
|
T | C | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02300.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.158+31441A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061363 | ||||||
| chr12:107061541
|
G | A | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+31263C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061541 | ||||||
| chr12:107061590
|
C | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+31214G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061590 | ||||||
| chr12:107061677
|
C | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+31127G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061677 | ||||||
| chr12:107061678
|
G | A | 1 | a0001c0001t0002g0287 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.158+31126C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061678 | ||||||
| chr12:107061712
|
T | C | 1 | a0001c0001t0007g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158+31092A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061712 | ||||||
| chr12:107061811
|
A | T | 5 | a0001c0001t0004g0164a0001c0001t0004g0165a0001c0001t0004g0166others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+30993T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061811 | ||||||
| chr12:107061826
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.158+30978A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061826 | ||||||
| chr12:107062025
|
CA | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 253 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.158+30778delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062025 | ||||||
| chr12:107062033
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0269a0001c0002t0003g0208 | 2 | HG02683.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.158+30751_158+3077 others(24): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062033 | ||||||
| chr12:107062041
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.158+30763T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062041 | ||||||
| chr12:107062130
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.158+30674C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062130 | ||||||
| chr12:107062165
|
A | T | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+30639T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062165 | ||||||
| chr12:107062215
|
T | C | 76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.158+30589A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062215 | ||||||
| chr12:107062322
|
T | A | 3 | a0001c0002t0003g0190a0001c0002t0003g0206a0001c0002t0003g0213 | 3 | HG02027.hp1 NA18963.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.158+30482A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062322 | ||||||
| chr12:107062468
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.158+30336G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062468 | ||||||
| chr12:107063009
|
C | A | 1 | a0001c0001t0002g0277 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.158+29795G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063009 | ||||||
| chr12:107063181
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.158+29623G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063181 | ||||||
| chr12:107063367
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+29437A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063367 | ||||||
| chr12:107063434
|
T | A | 1 | a0001c0001t0001g0144 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+29370A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063434 | ||||||
| chr12:107063469
|
A | C | 2 | a0001c0001t0002g0248a0001c0001t0002g0279 | 2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.158+29335T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063469 | ||||||
| chr12:107063550
|
G | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+29254C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063550 | ||||||
| chr12:107063599
|
T | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+29205A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063599 | ||||||
| chr12:107063828
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.158+28976G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063828 | ||||||
| chr12:107064060
|
T | C | 6 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(3): Show | 7 | HG01243.hp2 HG01884.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+28744A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064060 | ||||||
| chr12:107064114
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.158+28690T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064114 | ||||||
| chr12:107064115
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+28689G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064115 | ||||||
| chr12:107064120
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.158+28684C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064120 | ||||||
| chr12:107064125
|
G | A | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+28679C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064125 | ||||||
| chr12:107064168
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.158+28636C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064168 | ||||||
| chr12:107064400
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.158+28404C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064400 | ||||||
| chr12:107064634
|
TTAGAAA | T | 76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.158+28164_158+2816 others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064634 | ||||||
| chr12:107064778
|
C | T | 1 | a0001c0002t0003g0207 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.158+28026G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064778 | ||||||
| chr12:107064905
|
A | C | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+27899T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064905 | ||||||
| chr12:107064941
|
A | T | 1 | a0001c0001t0004g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.158+27863T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064941 | ||||||
| chr12:107064998
|
AT | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+27805delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064998 | ||||||
| chr12:107065026
|
G | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.158+27778C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065026 | ||||||
| chr12:107065164
|
C | T | 5 | a0001c0001t0004g0164a0001c0001t0004g0165a0001c0001t0004g0166others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+27640G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065164 | ||||||
| chr12:107065318
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.158+27486G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065318 | ||||||
| chr12:107065390
|
T | G | 2 | a0001c0001t0002g0244a0001c0001t0002g0290 | 2 | HG02132.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158+27414A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065390 | ||||||
| chr12:107065465
|
C | G | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+27339G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065465 | ||||||
| chr12:107065487
|
C | T | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+27317G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065487 | ||||||
| chr12:107066063
|
T | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+26741A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066063 | ||||||
| chr12:107066120
|
C | T | 61 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(58): Show | 63 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.158+26684G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066120 | ||||||
| chr12:107066405
|
T | G | 1 | a0001c0001t0002g0239 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.158+26399A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066405 | ||||||
| chr12:107066537
|
C | T | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+26267G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066537 | ||||||
| chr12:107066711
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.158+26093C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066711 | ||||||
| chr12:107066711
|
G | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+26093C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066711 | ||||||
| chr12:107066820
|
G | C | 1 | a0001c0002t0003g0196 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.158+25984C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066820 | ||||||
| chr12:107066935
|
G | A | 1 | a0001c0001t0002g0287 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.158+25869C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066935 | ||||||
| chr12:107067124
|
T | C | 1 | a0001c0001t0005g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158+25680A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067124 | ||||||
| chr12:107067184
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0064 | 3 | HG02683.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.158+25620C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067184 | ||||||
| chr12:107067441
|
T | C | 1 | a0001c0001t0014g0272 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158+25363A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067441 | ||||||
| chr12:107067563
|
C | CA | 19 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0298others(16): Show | 21 | HG00673.hp2 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.158+25240dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067563 | ||||||
| chr12:107067865
|
T | C | 1 | a0001c0002t0012g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.158+24939A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067865 | ||||||
| chr12:107067983
|
C | T | 73 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(70): Show | 75 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.158+24821G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067983 | ||||||
| chr12:107068147
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.158+24657C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068147 | ||||||
| chr12:107068254
|
G | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+24550C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068254 | ||||||
| chr12:107068457
|
C | T | 1 | a0001c0002t0003g0177 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.158+24347G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068457 | ||||||
| chr12:107068604
|
T | C | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+24200A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068604 | ||||||
| chr12:107068972
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.158+23832C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068972 | ||||||
| chr12:107069033
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.158+23771T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069033 | ||||||
| chr12:107069226
|
AT | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 168 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.158+23577delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069226 | ||||||
| chr12:107069256
|
G | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+23548C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069256 | ||||||
| chr12:107069350
|
G | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+23454C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069350 | ||||||
| chr12:107069352
|
G | A | 7 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0199others(4): Show | 7 | HG01361.hp2 HG02622.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+23452C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069352 | ||||||
| chr12:107069414
|
A | G | 1 | a0001c0002t0003g0172 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.158+23390T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069414 | ||||||
| chr12:107069574
|
G | GTA | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+23228_158+2322 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069574 | ||||||
| chr12:107069574
|
G | GTATATAT others(8): Show |
1 | a0001c0001t0003g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.158+23215_158+2322 others(19): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069574 | ||||||
| chr12:107069583
|
TAAAGTAT others(23): Show |
T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.158+23191_158+2322 others(34): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069583 | ||||||
| chr12:107069585
|
A | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+23219T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069585 | ||||||
| chr12:107069604
|
A | ATATATAT others(6): Show |
76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 79 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.158+23199_158+2320 others(17): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069604 | ||||||
| chr12:107069604
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+23199_158+2320 others(60): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069604 | ||||||
| chr12:107069611
|
TAA | T | 14 | a0001c0001t0001g0123a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 15 | HG01884.hp1 HG01981.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.158+23191_158+2319 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069611 | ||||||
| chr12:107069612
|
AAAAAGTA others(22): Show |
A | 1 | a0001c0001t0001g0128 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.158+23163_158+2319 others(33): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069612 | ||||||
| chr12:107069613
|
A | AAGTATAT others(4): Show |
1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+23190_158+2319 others(15): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069613 | ||||||
| chr12:107069613
|
A | T | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(132): Show | 139 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.158+23191T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069613 | ||||||
| chr12:107069614
|
AAAGT | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+23186_158+2318 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069614 | ||||||
| chr12:107069619
|
A | G | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+23185T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069619 | ||||||
| chr12:107069620
|
T | TATATATA others(8): Show |
3 | a0001c0001t0003g0193a0001c0001t0003g0224a0001c0001t0003g0225 | 3 | HG02572.hp1 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.158+23183_158+2318 others(19): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069620 | ||||||
| chr12:107069643
|
A | T | 1 | a0001c0002t0003g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.158+23161T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069643 | ||||||
| chr12:107069647
|
G | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+23157C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069647 | ||||||
| chr12:107069713
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.158+23091A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069713 | ||||||
| chr12:107069785
|
C | T | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+23019G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069785 | ||||||
| chr12:107069947
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18973.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.158+22857G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069947 | ||||||
| chr12:107070549
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.158+22255T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070549 | ||||||
| chr12:107070551
|
GAAAGA | G | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+22248_158+2225 others(9): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070551 | ||||||
| chr12:107070589
|
T | C | 1 | a0001c0001t0004g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.158+22215A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070589 | ||||||
| chr12:107070666
|
T | TTTTA | 33 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0016others(30): Show | 34 | HG00639.hp2 HG01928.hp2 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.158+22134_158+2213 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | ||||||
| chr12:107070666
|
T | TTTTATTT others(1): Show |
5 | a0001c0001t0002g0238a0001c0001t0002g0299a0001c0001t0011g0246others(2): Show | 5 | HG01943.hp1 HG02155.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+22130_158+2213 others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | ||||||
| chr12:107070666
|
TTTTA | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(65): Show | 72 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.158+22134_158+2213 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | ||||||
| chr12:107070666
|
TTTTATTT others(1): Show |
T | 10 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 11 | HG00140.hp2 HG00642.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.158+22130_158+2213 others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | ||||||
| chr12:107070666
|
TTTTATTT others(5): Show |
T | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+22126_158+2213 others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | ||||||
| chr12:107070761
|
C | T | 1 | a0001c0003t0006g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.158+22043G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070761 | ||||||
| chr12:107070803
|
G | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+22001C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070803 | ||||||
| chr12:107070867
|
AT | A | 8 | a0001c0001t0001g0095a0001c0001t0001g0114a0001c0001t0002g0304others(5): Show | 8 | HG01081.hp2 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+21936delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070867 | ||||||
| chr12:107070867
|
ATT | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 256 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.158+21935_158+2193 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070867 | ||||||
| chr12:107070917
|
G | A | 1 | a0001c0001t0004g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.158+21887C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070917 | ||||||
| chr12:107070984
|
G | A | 1 | a0001c0002t0003g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.158+21820C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070984 | ||||||
| chr12:107070993
|
A | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 252 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.158+21811T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070993 | ||||||
| chr12:107070993
|
A | T | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+21811T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070993 | ||||||
| chr12:107071118
|
C | G | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+21686G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107071118 | ||||||
| chr12:107071635
|
A | C | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+21169T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107071635 | ||||||
| chr12:107071851
|
G | A | 2 | a0001c0001t0004g0006a0001c0001t0004g0153 | 3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.158+20953C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107071851 | ||||||
| chr12:107072175
|
ACCTTT | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+20624_158+2062 others(9): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072175 | ||||||
| chr12:107072177
|
CTTTCT | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.158+20622_158+2062 others(9): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072177 | ||||||
| chr12:107072194
|
T | C | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+20610A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072194 | ||||||
| chr12:107072439
|
C | T | 104 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(101): Show | 108 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(105): Show |
intron_variant | MODIFIER | c.158+20365G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072439 | ||||||
| chr12:107072664
|
T | C | 1 | a0001c0001t0002g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.158+20140A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072664 | ||||||
| chr12:107072794
|
C | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+20010G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072794 | ||||||
| chr12:107072920
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.158+19884G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072920 | ||||||
| chr12:107072921
|
T | G | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+19883A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072921 | ||||||
| chr12:107072923
|
A | G | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+19881T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072923 | ||||||
| chr12:107073023
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG00639.hp1 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+19781C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073023 | ||||||
| chr12:107073082
|
AAAT | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(90): Show | 98 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.158+19719_158+1972 others(7): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073082 | ||||||
| chr12:107073104
|
C | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+19700G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073104 | ||||||
| chr12:107073138
|
TGGGAAAG others(2): Show |
T | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+19657_158+1966 others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073138 | ||||||
| chr12:107073243
|
C | CT | 7 | a0001c0001t0001g0093a0001c0001t0004g0006a0001c0001t0004g0153others(4): Show | 8 | HG02280.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+19560dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073243 | ||||||
| chr12:107073243
|
C | CTCT | 9 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(6): Show | 10 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.158+19560_158+1956 others(7): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073243 | ||||||
| chr12:107073328
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.158+19476C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073328 | ||||||
| chr12:107073424
|
A | T | 1 | a0001c0001t0002g0303 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.158+19380T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073424 | ||||||
| chr12:107073426
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.158+19378G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073426 | ||||||
| chr12:107073497
|
A | G | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+19307T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073497 | ||||||
| chr12:107073498
|
G | A | 1 | a0001c0002t0003g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.158+19306C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073498 | ||||||
| chr12:107073723
|
A | AGTCC | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+19077_158+1908 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073723 | ||||||
| chr12:107073728
|
G | A | 1 | a0001c0002t0012g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.158+19076C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073728 | ||||||
| chr12:107073907
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.158+18897C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073907 | ||||||
| chr12:107073935
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.158+18869T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073935 | ||||||
| chr12:107074051
|
T | A | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+18753A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074051 | ||||||
| chr12:107074058
|
T | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+18746A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074058 | ||||||
| chr12:107074108
|
A | G | 6 | a0001c0001t0004g0156a0001c0001t0004g0164a0001c0001t0004g0165others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+18696T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074108 | ||||||
| chr12:107074369
|
A | T | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+18435T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074369 | ||||||
| chr12:107074477
|
G | C | 1 | a0001c0002t0003g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.158+18327C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074477 | ||||||
| chr12:107074483
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.158+18321T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074483 | ||||||
| chr12:107074501
|
T | A | 3 | a0001c0002t0003g0217a0001c0002t0003g0228a0001c0002t0003g0229 | 3 | HG03490.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.158+18303A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074501 | ||||||
| chr12:107074562
|
A | T | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+18242T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074562 | ||||||
| chr12:107074678
|
C | T | 1 | a0001c0001t0007g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158+18126G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074678 | ||||||
| chr12:107074749
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.158+18055A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074749 | ||||||
| chr12:107074753
|
G | A | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+18051C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074753 | ||||||
| chr12:107074786
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0090others(2): Show | 6 | HG00408.hp2 NA18944.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+18018C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074786 | ||||||
| chr12:107074787
|
G | A | 3 | a0001c0002t0003g0218a0001c0002t0003g0219a0001c0002t0003g0220 | 3 | HG01074.hp1 HG01255.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.158+18017C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074787 | ||||||
| chr12:107075015
|
C | CA | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 130 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.158+17788dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075015 | ||||||
| chr12:107075015
|
C | CAA | 39 | a0001c0001t0001g0005a0001c0001t0001g0092a0001c0001t0001g0095others(36): Show | 41 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.158+17787_158+1778 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075015 | ||||||
| chr12:107075087
|
C | T | 1 | a0001c0002t0003g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.158+17717G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075087 | ||||||
| chr12:107075157
|
T | C | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+17647A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075157 | ||||||
| chr12:107075162
|
CA | C | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+17641delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075162 | ||||||
| chr12:107075168
|
T | G | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+17636A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075168 | ||||||
| chr12:107075190
|
A | G | 7 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170others(4): Show | 7 | HG01099.hp2 HG01256.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+17614T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075190 | ||||||
| chr12:107075544
|
G | C | 1 | a0001c0001t0002g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.158+17260C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075544 | ||||||
| chr12:107075670
|
G | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 8 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.158+17134C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075670 | ||||||
| chr12:107075928
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.158+16876A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075928 | ||||||
| chr12:107075994
|
G | A | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+16810C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075994 | ||||||
| chr12:107076081
|
C | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0290 | 2 | HG02132.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158+16723G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076081 | ||||||
| chr12:107076103
|
G | T | 1 | a0001c0001t0007g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.158+16701C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076103 | ||||||
| chr12:107076105
|
A | G | 1 | a0001c0002t0003g0175 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.158+16699T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076105 | ||||||
| chr12:107076337
|
G | A | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+16467C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076337 | ||||||
| chr12:107076370
|
G | A | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+16434C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076370 | ||||||
| chr12:107076618
|
GA | G | 25 | a0001c0001t0001g0017a0001c0001t0002g0284a0001c0001t0002g0287others(22): Show | 27 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.158+16185delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076618 | ||||||
| chr12:107076618
|
GAA | G | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+16184_158+1618 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076618 | ||||||
| chr12:107076634
|
A | C | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+16170T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076634 | ||||||
| chr12:107076695
|
A | G | 2 | a0001c0001t0011g0245a0001c0001t0011g0246 | 2 | HG02155.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.158+16109T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076695 | ||||||
| chr12:107076746
|
G | A | 3 | a0001c0001t0003g0193a0001c0001t0003g0224a0001c0001t0003g0225 | 3 | HG02572.hp1 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.158+16058C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076746 | ||||||
| chr12:107076770
|
G | A | 4 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0224others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+16034C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076770 | ||||||
| chr12:107076792
|
G | A | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+16012C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076792 | ||||||
| chr12:107076811
|
C | T | 3 | a0001c0001t0002g0244a0001c0001t0002g0290a0001c0001t0002g0301 | 3 | HG00558.hp2 HG02132.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158+15993G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076811 | ||||||
| chr12:107076977
|
C | T | 12 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(9): Show | 12 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+15827G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076977 | ||||||
| chr12:107077066
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.158+15738A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077066 | ||||||
| chr12:107077100
|
C | T | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+15704G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077100 | ||||||
| chr12:107077117
|
TCA | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG02083.hp1 NA18612.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+15685_158+1568 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077117 | ||||||
| chr12:107077162
|
A | AAC | 14 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(11): Show | 16 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.158+15640_158+1564 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077162 | ||||||
| chr12:107077291
|
T | C | 2 | a0001c0001t0004g0162a0001c0001t0004g0163 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.158+15513A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077291 | ||||||
| chr12:107077530
|
T | C | 1 | a0001c0002t0003g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.158+15274A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077530 | ||||||
| chr12:107077579
|
T | C | 2 | a0001c0002t0003g0189a0001c0002t0003g0222 | 2 | HG02145.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.158+15225A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077579 | ||||||
| chr12:107077604
|
T | A | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+15200A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077604 | ||||||
| chr12:107077653
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.158+15151A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077653 | ||||||
| chr12:107077694
|
G | C | 4 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287others(1): Show | 4 | HG02602.hp1 NA18943.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+15110C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077694 | ||||||
| chr12:107077777
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.158+15027G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077777 | ||||||
| chr12:107077786
|
A | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+15018T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077786 | ||||||
| chr12:107077826
|
C | G | 1 | a0001c0001t0002g0235 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.158+14978G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077826 | ||||||
| chr12:107078015
|
G | A | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+14789C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078015 | ||||||
| chr12:107078286
|
C | T | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+14518G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078286 | ||||||
| chr12:107078428
|
A | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.158+14376T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078428 | ||||||
| chr12:107078516
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+14288G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078516 | ||||||
| chr12:107078809
|
T | G | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+13995A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078809 | ||||||
| chr12:107078844
|
T | G | 1 | a0001c0002t0003g0223 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.158+13960A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078844 | ||||||
| chr12:107078926
|
T | C | 1 | a0001c0001t0004g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.158+13878A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078926 | ||||||
| chr12:107078929
|
C | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+13875G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078929 | ||||||
| chr12:107078950
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+13854C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078950 | ||||||
| chr12:107078954
|
T | A | 1 | a0001c0001t0004g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.158+13850A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078954 | ||||||
| chr12:107079099
|
A | AG | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+13704dupC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079099 | ||||||
| chr12:107079141
|
A | T | 2 | a0001c0001t0005g0231a0001c0001t0005g0233 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.158+13663T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079141 | ||||||
| chr12:107079276
|
G | A | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+13528C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079276 | ||||||
| chr12:107079426
|
CA | C | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+13377delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079426 | ||||||
| chr12:107079660
|
G | T | 1 | a0001c0001t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.158+13144C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079660 | ||||||
| chr12:107079662
|
C | T | 1 | a0001c0001t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.158+13142G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079662 | ||||||
| chr12:107079766
|
T | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+13038A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079766 | ||||||
| chr12:107080184
|
G | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+12620C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080184 | ||||||
| chr12:107080365
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18950.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.158+12439G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080365 | ||||||
| chr12:107080649
|
T | TA | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0155others(1): Show | 5 | HG02027.hp2 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+12154dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080649 | ||||||
| chr12:107080742
|
G | C | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+12062C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080742 | ||||||
| chr12:107080872
|
A | G | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+11932T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080872 | ||||||
| chr12:107080888
|
T | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+11916A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080888 | ||||||
| chr12:107081026
|
A | C | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+11778T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081026 | ||||||
| chr12:107081030
|
G | A | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+11774C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081030 | ||||||
| chr12:107081440
|
T | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+11364A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081440 | ||||||
| chr12:107081527
|
G | A | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+11277C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081527 | ||||||
| chr12:107081531
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.158+11273A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081531 | ||||||
| chr12:107081954
|
C | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 260 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.158+10850G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081954 | ||||||
| chr12:107082087
|
A | T | 1 | a0001c0001t0002g0241 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.158+10717T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082087 | ||||||
| chr12:107082213
|
G | C | 81 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+10591C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082213 | ||||||
| chr12:107082333
|
C | T | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+10471G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082333 | ||||||
| chr12:107082474
|
C | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+10330G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082474 | ||||||
| chr12:107082475
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+10329C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082475 | ||||||
| chr12:107082521
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.158+10283C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082521 | ||||||
| chr12:107082845
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.158+9959C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082845 | ||||||
| chr12:107082864
|
C | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.158+9940G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082864 | ||||||
| chr12:107082920
|
A | C | 2 | a0001c0001t0002g0289a0001c0004t0002g0288 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.158+9884T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082920 | ||||||
| chr12:107082938
|
T | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0093others(34): Show | 38 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.158+9866A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082938 | ||||||
| chr12:107083021
|
TCCCTCAG others(2): Show |
T | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+9774_158+9782d others(11): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083021 | ||||||
| chr12:107083089
|
T | C | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+9715A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083089 | ||||||
| chr12:107083234
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.158+9570A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083234 | ||||||
| chr12:107083448
|
A | G | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+9356T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083448 | ||||||
| chr12:107083450
|
A | G | 3 | a0001c0001t0002g0242a0001c0001t0002g0289a0001c0004t0002g0288 | 3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.158+9354T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083450 | ||||||
| chr12:107083595
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9209G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083595 | ||||||
| chr12:107083596
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9208T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083596 | ||||||
| chr12:107083603
|
T | A | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9201A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083603 | ||||||
| chr12:107083621
|
G | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+9183C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083621 | ||||||
| chr12:107083626
|
G | C | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9178C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083626 | ||||||
| chr12:107083627
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9177C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083627 | ||||||
| chr12:107083641
|
C | G | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9163G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083641 | ||||||
| chr12:107083642
|
C | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+9162G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083642 | ||||||
| chr12:107083643
|
G | C | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9161C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083643 | ||||||
| chr12:107083742
|
A | G | 1 | a0001c0001t0007g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158+9062T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083742 | ||||||
| chr12:107083743
|
T | C | 7 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG01361.hp1 HG01981.hp2 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.158+9061A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083743 | ||||||
| chr12:107083745
|
G | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.158+9059C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083745 | ||||||
| chr12:107083746
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.158+9058C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083746 | ||||||
| chr12:107083946
|
C | T | 5 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(2): Show | 6 | HG02280.hp1 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+8858G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083946 | ||||||
| chr12:107084196
|
GA | G | 2 | a0001c0001t0004g0006a0001c0001t0004g0153 | 3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.158+8607delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084196 | ||||||
| chr12:107084337
|
T | G | 2 | a0001c0001t0002g0289a0001c0004t0002g0288 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.158+8467A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084337 | ||||||
| chr12:107084810
|
A | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+7994T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084810 | ||||||
| chr12:107084909
|
T | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+7895A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084909 | ||||||
| chr12:107084915
|
T | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+7889A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084915 | ||||||
| chr12:107084973
|
C | CA | 29 | a0001c0001t0001g0027a0001c0001t0001g0129a0001c0001t0001g0130others(26): Show | 31 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.158+7830dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084973 | ||||||
| chr12:107084973
|
CA | C | 8 | a0001c0001t0002g0241a0001c0001t0002g0302a0001c0001t0004g0007others(5): Show | 9 | HG01884.hp1 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+7830delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084973 | ||||||
| chr12:107084986
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.158+7818T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084986 | ||||||
| chr12:107085065
|
GC | G | 8 | a0001c0002t0003g0172a0001c0002t0003g0182a0001c0002t0003g0183others(5): Show | 8 | NA18953.hp2 NA18956.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+7738delG | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085065 | ||||||
| chr12:107085141
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.158+7663C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085141 | ||||||
| chr12:107085235
|
C | T | 1 | a0001c0001t0007g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158+7569G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085235 | ||||||
| chr12:107085270
|
C | T | 2 | a0001c0002t0003g0180a0001c0002t0003g0181 | 2 | HG00099.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.158+7534G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085270 | ||||||
| chr12:107085273
|
C | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+7531G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085273 | ||||||
| chr12:107085277
|
C | G | 1 | a0001c0001t0001g0027 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.158+7527G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085277 | ||||||
| chr12:107085648
|
C | G | 6 | a0001c0001t0004g0156a0001c0001t0004g0164a0001c0001t0004g0165others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+7156G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085648 | ||||||
| chr12:107085730
|
T | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+7074A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085730 | ||||||
| chr12:107085747
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+7057G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085747 | ||||||
| chr12:107086354
|
G | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+6450C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086354 | ||||||
| chr12:107086400
|
TAAAAGAG others(4): Show |
T | 5 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0177others(2): Show | 5 | HG00735.hp1 HG01069.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+6393_158+6403d others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086400 | ||||||
| chr12:107086437
|
G | A | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+6367C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086437 | ||||||
| chr12:107086677
|
G | A | 76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(73): Show | 78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.158+6127C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086677 | ||||||
| chr12:107086698
|
A | G | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+6106T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086698 | ||||||
| chr12:107086766
|
C | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+6038G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086766 | ||||||
| chr12:107086809
|
A | ATTCTACT others(3): Show |
1 | a0001c0001t0002g0240 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.158+5985_158+5994d others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086809 | ||||||
| chr12:107086872
|
G | A | 1 | a0001c0002t0003g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.158+5932C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086872 | ||||||
| chr12:107086879
|
G | A | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+5925C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086879 | ||||||
| chr12:107087179
|
A | G | 1 | a0001c0001t0005g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+5625T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087179 | ||||||
| chr12:107087289
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.158+5515A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087289 | ||||||
| chr12:107087373
|
A | G | 2 | a0001c0002t0003g0173a0001c0002t0003g0174 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.158+5431T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087373 | ||||||
| chr12:107087511
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.158+5293A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087511 | ||||||
| chr12:107087635
|
T | C | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+5169A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087635 | ||||||
| chr12:107087673
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.158+5131C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087673 | ||||||
| chr12:107087811
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+4993C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087811 | ||||||
| chr12:107087837
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.158+4967G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087837 | ||||||
| chr12:107088027
|
A | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02257.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+4777T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088027 | ||||||
| chr12:107088072
|
C | T | 1 | a0001c0002t0012g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.158+4732G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088072 | ||||||
| chr12:107088356
|
G | C | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+4448C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088356 | ||||||
| chr12:107088393
|
C | G | 1 | a0001c0001t0015g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+4411G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088393 | ||||||
| chr12:107088492
|
AG | A | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(12): Show | 17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+4311delC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088492 | ||||||
| chr12:107088606
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.158+4198C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088606 | ||||||
| chr12:107088622
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.158+4182A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088622 | ||||||
| chr12:107088683
|
G | C | 1 | a0001c0001t0005g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.158+4121C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088683 | ||||||
| chr12:107088691
|
A | G | 3 | a0001c0001t0008g0152a0001c0001t0008g0169a0001c0001t0008g0170 | 3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+4113T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088691 | ||||||
| chr12:107088792
|
C | T | 1 | a0001c0002t0003g0172 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.158+4012G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088792 | ||||||
| chr12:107088812
|
G | A | 11 | a0001c0001t0004g0007a0001c0001t0004g0156a0001c0001t0004g0161others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+3992C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088812 | ||||||
| chr12:107088889
|
A | G | 78 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0235others(75): Show | 80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+3915T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088889 | ||||||
| chr12:107089029
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.158+3775A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089029 | ||||||
| chr12:107089189
|
T | A | 4 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0304others(1): Show | 4 | HG03195.hp1 HG03579.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+3615A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089189 | ||||||
| chr12:107089373
|
T | TC | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+3430_158+3431i others(3): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089373 | ||||||
| chr12:107089375
|
C | A | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+3429G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089375 | ||||||
| chr12:107089401
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.158+3403G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089401 | ||||||
| chr12:107089537
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+3267T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089537 | ||||||
| chr12:107089646
|
C | T | 3 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024 | 3 | HG02818.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.158+3158G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089646 | ||||||
| chr12:107089647
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.158+3157C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089647 | ||||||
| chr12:107089798
|
A | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+3006T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089798 | ||||||
| chr12:107089860
|
C | A | 3 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0155 | 4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+2944G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089860 | ||||||
| chr12:107090041
|
C | T | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+2763G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090041 | ||||||
| chr12:107090074
|
C | T | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+2730G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090074 | ||||||
| chr12:107090096
|
C | CT | 18 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0153others(15): Show | 20 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.158+2707dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090096 | ||||||
| chr12:107090110
|
G | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.158+2694C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090110 | ||||||
| chr12:107090295
|
A | G | 1 | a0001c0001t0002g0239 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.158+2509T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090295 | ||||||
| chr12:107090320
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00597.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.158+2484C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090320 | ||||||
| chr12:107090337
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.158+2467G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090337 | ||||||
| chr12:107090423
|
G | T | 1 | a0001c0001t0002g0238 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.158+2381C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090423 | ||||||
| chr12:107090600
|
C | T | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+2204G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090600 | ||||||
| chr12:107090872
|
G | GAAC | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+1929_158+1931d others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090872 | ||||||
| chr12:107090901
|
C | T | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+1903G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090901 | ||||||
| chr12:107090960
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.158+1844T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090960 | ||||||
| chr12:107091007
|
A | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG02056.hp2 HG02155.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+1797T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091007 | ||||||
| chr12:107091039
|
T | C | 3 | a0001c0001t0005g0231a0001c0001t0005g0232a0001c0001t0005g0233 | 3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+1765A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091039 | ||||||
| chr12:107091045
|
CT | C | 6 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(3): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+1758delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091045 | ||||||
| chr12:107091056
|
T | C | 4 | a0001c0003t0006g0157a0001c0003t0006g0158a0001c0003t0006g0159others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+1748A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091056 | ||||||
| chr12:107091103
|
G | C | 1 | a0001c0001t0002g0307 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.158+1701C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091103 | ||||||
| chr12:107091188
|
C | T | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+1616G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091188 | ||||||
| chr12:107091191
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+1613G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091191 | ||||||
| chr12:107091362
|
A | G | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+1442T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091362 | ||||||
| chr12:107091433
|
C | T | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+1371G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091433 | ||||||
| chr12:107091445
|
T | C | 1 | a0001c0001t0005g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+1359A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091445 | ||||||
| chr12:107091488
|
GCTT | G | 5 | a0001c0001t0004g0007a0001c0001t0004g0161a0001c0001t0004g0162others(2): Show | 6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+1313_158+1315d others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091488 | ||||||
| chr12:107091657
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.158+1147A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091657 | ||||||
| chr12:107091775
|
A | G | 2 | a0001c0001t0004g0006a0001c0001t0004g0153 | 3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.158+1029T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091775 | ||||||
| chr12:107091781
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01256.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.158+1023G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091781 | ||||||
| chr12:107091807
|
G | A | 5 | a0001c0001t0004g0164a0001c0001t0004g0165a0001c0001t0004g0166others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+997C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091807 | ||||||
| chr12:107092197
|
C | T | 4 | a0001c0001t0004g0006a0001c0001t0004g0153a0001c0001t0004g0154others(1): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+607G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092197 | ||||||
| chr12:107092210
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.158+594G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092210 | ||||||
| chr12:107092265
|
A | G | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.158+539T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092265 | ||||||
| chr12:107092290
|
C | A | 2 | a0001c0001t0008g0169a0001c0001t0008g0170 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+514G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092290 | ||||||
| chr12:107092555
|
A | C | 1 | a0001c0001t0008g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+249T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092555 | ||||||
| chr12:107092729
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+75C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092729 | ||||||
| chr12:107092791
|
G | A | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+13C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092791 |