Search by Gene
| geneid | 124801 |
|---|---|
| ensemblid | ENSG00000161654.10 |
| hgncid | 26407 |
| symbol | LSM12 |
| name | LSM12 homolog |
| refseq_nuc | NM_001371445.1 |
| refseq_prot | NP_001358374.1 |
| ensembl_nuc | ENST00000293406.8 |
| ensembl_prot | ENSP00000293406.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 44034328 |
| end | 44066671 |
| strand | - |
| ver | v1.2 |
| region | chr17:44034328-44066671 |
| region5000 | chr17:44029328-44071671 |
| regionname0 | LSM12_chr17_44034328_44066671 |
| regionname5000 | LSM12_chr17_44029328_44071671 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 195 | 294 | 84 | 62 | 114 | 8 | 24 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0002 | 0/0 | 195 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 588 | 290 | 80 | 62 | 114 | 8 | 24 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| c0002 | 0/0 | 588 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| c0003 | 0/0 | 588 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1966 | 191 | 38 | 37 | 94 | 4 | 17 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0002 | 0/0 | 1967 | 48 | 22 | 12 | 8 | 2 | 4 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0003 | 0/0 | 1965 | 23 | 12 | 5 | 3 | 1 | 2 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0004 | 0/0 | 1966 | 7 | 0 | 6 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0005 | 0/0 | 1964 | 7 | 0 | 0 | 7 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0006 | 0/0 | 1966 | 4 | 3 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0007 | 0/0 | 1966 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0008 | 0/0 | 1966 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0009 | 0/0 | 1962 | 3 | 3 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0010 | 1/0 | 1965 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0011 | 0/0 | 1966 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0012 | 0/0 | 1967 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0013 | 0/0 | 1967 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0014 | 0/0 | 1967 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0015 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| t0016 | 0/0 | 1966 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 1 | 2 | 2 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0003 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 290 | 80 | 62 | 114 | 8 | 24 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 191 | 38 | 37 | 94 | 4 | 17 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 44 | 18 | 12 | 8 | 2 | 4 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 19 | 8 | 5 | 3 | 1 | 2 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0001c0003t0002 | a0001 | c0003 | t0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| a0002c0002t0003 | a0002 | c0002 | t0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 6 | 1 | 2 | 2 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0230 | a0001 | c0001 | t0001 | g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0236 | a0001 | c0001 | t0001 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0238 | a0001 | c0001 | t0001 | g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0241 | a0001 | c0001 | t0001 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0001g0266 | a0001 | c0001 | t0001 | g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0075 | a0001 | c0001 | t0002 | g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0094 | a0001 | c0001 | t0002 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0111 | a0001 | c0001 | t0002 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0137 | a0001 | c0001 | t0002 | g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0145 | a0001 | c0001 | t0002 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0182 | a0001 | c0001 | t0002 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0188 | a0001 | c0001 | t0002 | g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0199 | a0001 | c0001 | t0002 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0201 | a0001 | c0001 | t0002 | g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0246 | a0001 | c0001 | t0002 | g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0247 | a0001 | c0001 | t0002 | g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0248 | a0001 | c0001 | t0002 | g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0249 | a0001 | c0001 | t0002 | g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0250 | a0001 | c0001 | t0002 | g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0251 | a0001 | c0001 | t0002 | g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0252 | a0001 | c0001 | t0002 | g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0254 | a0001 | c0001 | t0002 | g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0255 | a0001 | c0001 | t0002 | g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0256 | a0001 | c0001 | t0002 | g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0257 | a0001 | c0001 | t0002 | g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0258 | a0001 | c0001 | t0002 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0259 | a0001 | c0001 | t0002 | g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0260 | a0001 | c0001 | t0002 | g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0261 | a0001 | c0001 | t0002 | g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0262 | a0001 | c0001 | t0002 | g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0265 | a0001 | c0001 | t0002 | g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0267 | a0001 | c0001 | t0002 | g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0268 | a0001 | c0001 | t0002 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0270 | a0001 | c0001 | t0002 | g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0271 | a0001 | c0001 | t0002 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0272 | a0001 | c0001 | t0002 | g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0273 | a0001 | c0001 | t0002 | g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0274 | a0001 | c0001 | t0002 | g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0002g0275 | a0001 | c0001 | t0002 | g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0004 | a0001 | c0001 | t0003 | g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0017 | a0001 | c0001 | t0003 | g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0018 | a0001 | c0001 | t0003 | g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0022 | a0001 | c0001 | t0003 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0023 | a0001 | c0001 | t0003 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0031 | a0001 | c0001 | t0003 | g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0035 | a0001 | c0001 | t0003 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0036 | a0001 | c0001 | t0003 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0076 | a0001 | c0001 | t0003 | g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0132 | a0001 | c0001 | t0003 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0146 | a0001 | c0001 | t0003 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0147 | a0001 | c0001 | t0003 | g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0148 | a0001 | c0001 | t0003 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0157 | a0001 | c0001 | t0003 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0253 | a0001 | c0001 | t0003 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0263 | a0001 | c0001 | t0003 | g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0264 | a0001 | c0001 | t0003 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0003g0269 | a0001 | c0001 | t0003 | g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0004g0007 | a0001 | c0001 | t0004 | g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0004g0175 | a0001 | c0001 | t0004 | g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0004g0177 | a0001 | c0001 | t0004 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0004g0196 | a0001 | c0001 | t0004 | g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0004g0200 | a0001 | c0001 | t0004 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0004g0216 | a0001 | c0001 | t0004 | g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0005g0104 | a0001 | c0001 | t0005 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0005g0105 | a0001 | c0001 | t0005 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0005g0166 | a0001 | c0001 | t0005 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0005g0174 | a0001 | c0001 | t0005 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0005g0179 | a0001 | c0001 | t0005 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0005g0244 | a0001 | c0001 | t0005 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0005g0245 | a0001 | c0001 | t0005 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0006g0144 | a0001 | c0001 | t0006 | g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0006g0150 | a0001 | c0001 | t0006 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0006g0154 | a0001 | c0001 | t0006 | g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0006g0156 | a0001 | c0001 | t0006 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0007g0026 | a0001 | c0001 | t0007 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0007g0027 | a0001 | c0001 | t0007 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0007g0028 | a0001 | c0001 | t0007 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0007g0032 | a0001 | c0001 | t0007 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0008g0012 | a0001 | c0001 | t0008 | g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0008g0278 | a0001 | c0001 | t0008 | g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0008g0279 | a0001 | c0001 | t0008 | g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0009g0100 | a0001 | c0001 | t0009 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0009g0101 | a0001 | c0001 | t0009 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0009g0115 | a0001 | c0001 | t0009 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0010g0158 | a0001 | c0001 | t0010 | g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0011g0239 | a0001 | c0001 | t0011 | g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0012g0180 | a0001 | c0001 | t0012 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0013g0190 | a0001 | c0001 | t0013 | g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0014g0029 | a0001 | c0001 | t0014 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0015g0276 | a0001 | c0001 | t0015 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0001t0016g0277 | a0001 | c0001 | t0016 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0003t0002g0106 | a0001 | c0003 | t0002 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0003t0002g0107 | a0001 | c0003 | t0002 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0003t0002g0108 | a0001 | c0003 | t0002 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0001c0003t0002g0109 | a0001 | c0003 | t0002 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0002c0002t0003g0019 | a0002 | c0002 | t0003 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0002c0002t0003g0020 | a0002 | c0002 | t0003 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0002c0002t0003g0021 | a0002 | c0002 | t0003 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| a0002c0002t0003g0024 | a0002 | c0002 | t0003 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0261 | EUR | GBR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0200 | EUR | GBR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0076 | EUR | FIN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01257 | hp1 | a0001 | c0001 | t0012 | g0180 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02129 | hp2 | a0001 | c0001 | t0016 | g0277 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0021 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0239 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0108 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0029 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0101 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0106 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0115 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0019 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0190 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | LSM12_chr17_44029328_44071671 | LSM12 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18988 | hp2 | a0001 | c0001 | t0015 | g0276 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0020 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0027 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ASW | LSM12_chr17_44029328_44071671 | LSM12 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | LSM12_chr17_44029328_44071671 | LSM12 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | TSI | LSM12_chr17_44029328_44071671 | LSM12 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0107 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0278 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | USA | LSM12_chr17_44029328_44071671 | LSM12 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | USA | LSM12_chr17_44029328_44071671 | LSM12 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | LSM12_chr17_44029328_44071671 | LSM12 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | LSM12_chr17_44029328_44071671 | LSM12 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0207 | REF | REF | LSM12_chr17_44029328_44071671 | LSM12 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0158 | REF | REF | LSM12_chr17_44029328_44071671 | LSM12 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44036279
|
C | G | 1 | a0002 | 4 | HG02257.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.517G>C | p.Val173Leu | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 601/2552 | 517/588 | 173/195 | chr17 | 44036279 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44037523
|
T | C | 1 | a0001c0003 | 4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.384A>G | p.Lys128Lys | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/5 | 468/2552 | 384/588 | 128/195 | chr17 | 44037523 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44034360
|
GCCGA | G | 1 | a0001c0001t0009 | 3 | HG02965.hp2 HG03098.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1844_*1847delTCGG | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1844 | chr17 | 44034360 | |||||
| chr17:44034464
|
C | A | 1 | a0001c0001t0013 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1744G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1744 | chr17 | 44034464 | |||||
| chr17:44034466
|
C | T | 2 | a0001c0001t0004a0001c0001t0012 | 8 | HG00099.hp2 HG00735.hp1 HG01071.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1742G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1742 | chr17 | 44034466 | |||||
| chr17:44034568
|
T | C | 17 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*1640A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1640 | chr17 | 44034568 | |||||
| chr17:44034966
|
G | A | 2 | a0001c0001t0007a0001c0001t0014 | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1242C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1242 | chr17 | 44034966 | |||||
| chr17:44035139
|
A | G | 1 | a0001c0001t0011 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1069 | chr17 | 44035139 | |||||
| chr17:44035270
|
ACT | A | 1 | a0001c0001t0005 | 7 | NA18941.hp2 NA18951.hp1 NA18952.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*936_*937delAG | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 936 | chr17 | 44035270 | |||||
| chr17:44035677
|
C | CA | 10 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(7): Show | 223 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*530dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 530 | chr17 | 44035677 | |||||
| chr17:44035677
|
C | CAA | 5 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(2): Show | 51 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*529_*530dupTT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 530 | chr17 | 44035677 | |||||
| chr17:44035711
|
A | C | 1 | a0001c0001t0006 | 4 | HG01169.hp2 HG02717.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*497T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 497 | chr17 | 44035711 | |||||
| chr17:44066608
|
CGGCGGCG others(15): Show |
C | 1 | a0001c0001t0015 | 1 | NA18988.hp2 | 5_prime_UTR_variant | MODIFIER | c.-43_-22delCGCTGCTG others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/5 | 22 | chr17 | 44066608 | |||||
| chr17:44066656
|
G | A | 1 | a0001c0001t0016 | 1 | HG02129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-69C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/5 | 69 | chr17 | 44066656 | |||||
| chr17:44066669
|
G | C | 1 | a0001c0001t0008 | 4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-82C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/5 | 82 | chr17 | 44066669 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44036439
|
T | C | 25 | a0001c0001t0001g0266a0001c0001t0002g0015a0001c0001t0002g0252others(22): Show | 25 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.496-139A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036439 | ||||||
| chr17:44036440
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496-140A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036440 | ||||||
| chr17:44036689
|
G | GA | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 115 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.496-390dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036689 | ||||||
| chr17:44036772
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496-472G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036772 | ||||||
| chr17:44036830
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.496-530G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036830 | ||||||
| chr17:44037029
|
G | A | 3 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0115 | 3 | HG02965.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.495+383C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44037029 | ||||||
| chr17:44037091
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.495+321C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44037091 | ||||||
| chr17:44037304
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(103): Show | 116 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.495+108A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44037304 | ||||||
| chr17:44037600
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0228 | 2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.369-62C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037600 | ||||||
| chr17:44037660
|
C | G | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.369-122G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037660 | ||||||
| chr17:44037740
|
A | G | 1 | a0001c0001t0011g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-202T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037740 | ||||||
| chr17:44037818
|
C | T | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-280G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037818 | ||||||
| chr17:44037915
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02559.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.369-377T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037915 | ||||||
| chr17:44037933
|
C | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0121 | 2 | HG03239.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.369-395G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037933 | ||||||
| chr17:44037977
|
G | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-439C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037977 | ||||||
| chr17:44038010
|
T | C | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0002g0111others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-472A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038010 | ||||||
| chr17:44038012
|
G | A | 4 | a0002c0002t0003g0019a0002c0002t0003g0020a0002c0002t0003g0021others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-474C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038012 | ||||||
| chr17:44038070
|
C | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 15 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.369-532G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038070 | ||||||
| chr17:44038094
|
A | T | 1 | a0001c0001t0003g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.369-556T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038094 | ||||||
| chr17:44038102
|
G | A | 1 | a0002c0002t0003g0020 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.369-564C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038102 | ||||||
| chr17:44038278
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.369-740C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038278 | ||||||
| chr17:44038338
|
A | G | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-800T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038338 | ||||||
| chr17:44038351
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.369-813C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038351 | ||||||
| chr17:44038355
|
C | CA | 13 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0185others(10): Show | 13 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.369-818dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038355 | ||||||
| chr17:44038383
|
G | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG02109.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.369-845C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038383 | ||||||
| chr17:44038660
|
AAG | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0167others(32): Show | 38 | HG00438.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.369-1124_369-1123d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038660 | ||||||
| chr17:44038688
|
C | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.369-1150G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038688 | ||||||
| chr17:44038731
|
G | C | 7 | a0001c0001t0008g0012a0001c0001t0008g0278a0001c0001t0008g0279others(4): Show | 8 | HG02723.hp1 HG02886.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-1193C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038731 | ||||||
| chr17:44038767
|
T | C | 1 | a0001c0001t0002g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.369-1229A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038767 | ||||||
| chr17:44038783
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.369-1245A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038783 | ||||||
| chr17:44038896
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.368+1251A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038896 | ||||||
| chr17:44038941
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.368+1206G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038941 | ||||||
| chr17:44038953
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.368+1194A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038953 | ||||||
| chr17:44038967
|
G | A | 22 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(19): Show | 22 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.368+1180C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038967 | ||||||
| chr17:44039222
|
T | C | 3 | a0001c0001t0008g0012a0001c0001t0008g0278a0001c0001t0008g0279 | 4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+925A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039222 | ||||||
| chr17:44039268
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.368+879A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039268 | ||||||
| chr17:44039306
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.368+841G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039306 | ||||||
| chr17:44039319
|
T | C | 2 | a0001c0001t0007g0026a0001c0001t0007g0027 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.368+828A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039319 | ||||||
| chr17:44039353
|
C | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(77): Show | 88 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.368+794G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039353 | ||||||
| chr17:44039365
|
C | CT | 108 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.368+781dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | ||||||
| chr17:44039365
|
C | CTT | 57 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0034others(54): Show | 60 | HG00438.hp1 HG00597.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.368+780_368+781dup others(2): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | ||||||
| chr17:44039365
|
C | CTTT | 7 | a0001c0001t0001g0136a0001c0001t0001g0236a0001c0001t0002g0199others(4): Show | 7 | HG01891.hp1 HG02135.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+779_368+781dup others(3): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | ||||||
| chr17:44039365
|
CT | C | 27 | a0001c0001t0001g0025a0001c0001t0001g0046a0001c0001t0001g0050others(24): Show | 28 | HG00099.hp1 HG01069.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.368+781delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | ||||||
| chr17:44039365
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0014g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.368+765_368+781del others(17): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | ||||||
| chr17:44039405
|
C | T | 2 | a0001c0001t0007g0028a0001c0001t0007g0032 | 2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.368+742G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039405 | ||||||
| chr17:44039430
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.368+717C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039430 | ||||||
| chr17:44039482
|
C | T | 3 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0148 | 3 | HG01106.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.368+665G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039482 | ||||||
| chr17:44040003
|
C | G | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.368+144G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040003 | ||||||
| chr17:44040011
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.368+136A>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040011 | ||||||
| chr17:44040081
|
T | A | 1 | a0001c0001t0007g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.368+66A>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040081 | ||||||
| chr17:44040091
|
C | T | 2 | a0001c0001t0006g0144a0001c0001t0006g0150 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.368+56G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040091 | ||||||
| chr17:44040099
|
C | A | 1 | a0001c0001t0007g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.368+48G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040099 | ||||||
| chr17:44040118
|
G | A | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.368+29C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040118 | ||||||
| chr17:44040403
|
A | G | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-147T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040403 | ||||||
| chr17:44040449
|
G | GTTCC | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-197_259-194dup others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040449 | ||||||
| chr17:44040479
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.259-223A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040479 | ||||||
| chr17:44040488
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.259-232A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040488 | ||||||
| chr17:44040681
|
A | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 15 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-425T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040681 | ||||||
| chr17:44040819
|
C | CA | 10 | a0001c0001t0001g0127a0001c0001t0001g0164a0001c0001t0001g0165others(7): Show | 10 | HG00280.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-564dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040819 | ||||||
| chr17:44040819
|
C | CAA | 18 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0255others(15): Show | 18 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.259-565_259-564dup others(2): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040819 | ||||||
| chr17:44040938
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0003g0035 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.259-682C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040938 | ||||||
| chr17:44040996
|
C | A | 1 | a0001c0001t0008g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-740G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040996 | ||||||
| chr17:44041020
|
T | TACAC | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0002g0111others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-768_259-765dup others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041020 | ||||||
| chr17:44041020
|
T | TACACAC | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0002g0037others(1): Show | 4 | HG02145.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-770_259-765dup others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041020 | ||||||
| chr17:44041127
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.259-871G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041127 | ||||||
| chr17:44041273
|
TA | T | 40 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0043others(37): Show | 40 | HG00621.hp2 HG00639.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.259-1018delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041273 | ||||||
| chr17:44041273
|
TAAA | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0143a0001c0001t0001g0161others(18): Show | 22 | HG00639.hp2 HG01099.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.259-1020_259-1018d others(5): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041273 | ||||||
| chr17:44041273
|
TAAAAA | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0034others(43): Show | 48 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.259-1022_259-1018d others(7): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041273 | ||||||
| chr17:44041273
|
TAAAAAAA | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0126a0001c0001t0001g0127others(12): Show | 15 | HG00558.hp1 HG01123.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-1024_259-1018d others(9): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041273 | ||||||
| chr17:44041277
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0006g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.259-1032_259-1022d others(13): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041277 | ||||||
| chr17:44041279
|
A | C | 1 | a0001c0001t0001g0142 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.259-1023T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041279 | ||||||
| chr17:44041279
|
AAAAAAAA others(2): Show |
A | 10 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0153others(7): Show | 10 | HG01081.hp2 HG02040.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-1032_259-1024d others(11): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041279 | ||||||
| chr17:44041279
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0162 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259-1040_259-1024d others(19): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041279 | ||||||
| chr17:44041279
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.259-1046_259-1024d others(25): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041279 | ||||||
| chr17:44041280
|
A | AC | 3 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0003g0147 | 3 | HG01257.hp2 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259-1025_259-1024i others(3): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041280 | ||||||
| chr17:44041281
|
AAAAAAAC | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 31 | HG00597.hp1 HG00738.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.259-1032_259-1026d others(9): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041281 | ||||||
| chr17:44041282
|
A | C | 7 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-1026T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041282 | ||||||
| chr17:44041283
|
AAAAAC | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(32): Show | 43 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.259-1032_259-1028d others(7): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041283 | ||||||
| chr17:44041283
|
AAAAACAA others(10): Show |
A | 1 | a0001c0001t0008g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-1044_259-1028d others(19): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041283 | ||||||
| chr17:44041284
|
A | AAAC | 12 | a0001c0001t0002g0252a0001c0001t0002g0254a0001c0001t0002g0257others(9): Show | 12 | HG00099.hp1 HG00738.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.259-1029_259-1028i others(5): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041284 | ||||||
| chr17:44041284
|
A | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0140a0001c0001t0001g0143others(21): Show | 25 | HG00621.hp2 HG01169.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-1028T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041284 | ||||||
| chr17:44041284
|
AAAACAAA others(3): Show |
A | 1 | a0001c0001t0001g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.259-1038_259-1029d others(12): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041284 | ||||||
| chr17:44041285
|
AAACAAAC | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0077others(4): Show | 7 | HG01109.hp2 HG01175.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-1036_259-1030d others(9): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041285 | ||||||
| chr17:44041285
|
AAACAAAC others(2): Show |
A | 7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0078others(4): Show | 7 | HG02132.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-1038_259-1030d others(11): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041285 | ||||||
| chr17:44041285
|
AAACAAAC others(4): Show |
A | 1 | a0001c0001t0001g0118 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.259-1040_259-1030d others(13): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041285 | ||||||
| chr17:44041285
|
AAACAAAC others(6): Show |
A | 8 | a0001c0001t0001g0083a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG00735.hp2 HG02698.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1042_259-1030d others(15): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041285 | ||||||
| chr17:44041286
|
A | ACAAAC | 3 | a0001c0001t0001g0266a0001c0001t0002g0273a0001c0001t0003g0253 | 3 | HG01993.hp2 NA18984.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.259-1031_259-1030i others(7): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041286 | ||||||
| chr17:44041286
|
A | C | 55 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0130others(52): Show | 56 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.259-1030T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041286 | ||||||
| chr17:44041290
|
A | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(138): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.259-1034T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041290 | ||||||
| chr17:44041290
|
AAC | A | 15 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0064others(12): Show | 16 | HG00639.hp1 HG01496.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-1036_259-1035d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041290 | ||||||
| chr17:44041290
|
AACACAC | A | 3 | a0001c0001t0003g0018a0002c0002t0003g0019a0002c0002t0003g0021 | 3 | HG00741.hp1 HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.259-1040_259-1035d others(8): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041290 | ||||||
| chr17:44041290
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0001g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.259-1046_259-1035d others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041290 | ||||||
| chr17:44041294
|
C | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(31): Show | 42 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.259-1038G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041294 | ||||||
| chr17:44041296
|
C | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0077others(4): Show | 7 | HG01109.hp2 HG01175.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-1040G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041296 | ||||||
| chr17:44041298
|
C | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(5): Show | 8 | HG02132.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1042G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041298 | ||||||
| chr17:44041300
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.259-1044G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041300 | ||||||
| chr17:44041302
|
C | A | 8 | a0001c0001t0001g0083a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG00735.hp2 HG02698.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1046G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041302 | ||||||
| chr17:44041318
|
C | A | 4 | a0001c0003t0002g0106a0001c0003t0002g0107a0001c0003t0002g0108others(1): Show | 4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-1062G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041318 | ||||||
| chr17:44041324
|
C | A | 3 | a0001c0001t0007g0028a0001c0001t0007g0032a0001c0001t0014g0029 | 3 | HG02723.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.259-1068G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041324 | ||||||
| chr17:44041326
|
C | A | 3 | a0001c0001t0002g0273a0001c0001t0007g0026a0001c0001t0007g0027 | 3 | HG02145.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259-1070G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041326 | ||||||
| chr17:44041326
|
CACACACA others(1): Show |
C | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp1 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1078_259-1071d others(10): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041326 | ||||||
| chr17:44041328
|
C | A | 16 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 16 | HG00438.hp1 HG00741.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-1072G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041328 | ||||||
| chr17:44041328
|
C | CACACACA others(5): Show |
1 | a0001c0001t0002g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-1073_259-1072i others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041328 | ||||||
| chr17:44041328
|
CACACAA | C | 3 | a0001c0001t0001g0049a0001c0001t0007g0026a0001c0001t0007g0027 | 3 | HG01243.hp2 HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.259-1078_259-1073d others(8): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041328 | ||||||
| chr17:44041330
|
C | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 146 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.259-1074G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041330 | ||||||
| chr17:44041330
|
CACAA | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02559.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.259-1078_259-1075d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041330 | ||||||
| chr17:44041332
|
C | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0210 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.259-1076G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041332 | ||||||
| chr17:44041332
|
CAA | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0098others(3): Show | 6 | HG01192.hp2 HG02895.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1078_259-1077d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041332 | ||||||
| chr17:44041334
|
A | AACAC | 4 | a0001c0001t0001g0054a0001c0001t0002g0257a0001c0001t0002g0258others(1): Show | 4 | HG03579.hp2 NA19064.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1082_259-1079d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041334 | ||||||
| chr17:44041334
|
A | AACACAC | 10 | a0001c0001t0002g0252a0001c0001t0002g0256a0001c0001t0002g0259others(7): Show | 10 | HG00099.hp1 HG00738.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-1084_259-1079d others(8): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041334 | ||||||
| chr17:44041334
|
A | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 166 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.259-1078T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041334 | ||||||
| chr17:44041336
|
C | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0003g0031 | 3 | HG02145.hp1 HG03540.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.259-1080G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041336 | ||||||
| chr17:44041879
|
C | CTGGAGAC others(28): Show |
1 | a0001c0001t0001g0173 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.259-1658_259-1624d others(37): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041879 | ||||||
| chr17:44042024
|
C | T | 8 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0069others(5): Show | 8 | HG00438.hp2 HG02165.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1768G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042024 | ||||||
| chr17:44042039
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.259-1783A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042039 | ||||||
| chr17:44042055
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.259-1799C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042055 | ||||||
| chr17:44042057
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.259-1801G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042057 | ||||||
| chr17:44042058
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.259-1802T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042058 | ||||||
| chr17:44042060
|
G | C | 8 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0069others(5): Show | 8 | HG00438.hp2 HG02165.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1804C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042060 | ||||||
| chr17:44042240
|
T | C | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-1984A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042240 | ||||||
| chr17:44042495
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-2239C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042495 | ||||||
| chr17:44042502
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.259-2246G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042502 | ||||||
| chr17:44042566
|
AT | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(268): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.259-2311delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042566 | ||||||
| chr17:44042587
|
C | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0001g0185others(2): Show | 5 | NA18957.hp2 NA18988.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-2331G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042587 | ||||||
| chr17:44042603
|
C | CGCCCAGG others(8): Show |
261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.259-2348_259-2347i others(17): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042603 | ||||||
| chr17:44042626
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.259-2370C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042626 | ||||||
| chr17:44042710
|
G | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.259-2454C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042710 | ||||||
| chr17:44042721
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.259-2465G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042721 | ||||||
| chr17:44042782
|
T | C | 23 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(20): Show | 23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.259-2526A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042782 | ||||||
| chr17:44042915
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.259-2659G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042915 | ||||||
| chr17:44042954
|
C | A | 2 | a0001c0003t0002g0106a0001c0003t0002g0109 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-2698G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042954 | ||||||
| chr17:44043089
|
G | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-2833C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043089 | ||||||
| chr17:44043125
|
G | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0081 | 2 | HG00438.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.259-2869C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043125 | ||||||
| chr17:44043311
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.259-3055A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043311 | ||||||
| chr17:44043315
|
G | A | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-3059C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043315 | ||||||
| chr17:44043406
|
G | A | 1 | a0001c0001t0008g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-3150C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043406 | ||||||
| chr17:44043548
|
C | CT | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(124): Show | 137 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.259-3293dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043548 | ||||||
| chr17:44043806
|
T | TA | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0194others(8): Show | 11 | HG00621.hp2 HG01257.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.259-3551dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043806 | ||||||
| chr17:44043847
|
G | A | 3 | a0001c0001t0008g0012a0001c0001t0008g0278a0001c0001t0008g0279 | 4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-3591C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043847 | ||||||
| chr17:44043921
|
G | A | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-3665C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043921 | ||||||
| chr17:44043947
|
C | A | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-3691G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043947 | ||||||
| chr17:44044022
|
C | T | 3 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0275 | 3 | HG01081.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.259-3766G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044022 | ||||||
| chr17:44044260
|
A | C | 1 | a0001c0001t0002g0088 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259-4004T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044260 | ||||||
| chr17:44044322
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.259-4066T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044322 | ||||||
| chr17:44044328
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.259-4072A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044328 | ||||||
| chr17:44044353
|
C | G | 1 | a0001c0001t0002g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259-4097G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044353 | ||||||
| chr17:44044440
|
A | T | 1 | a0001c0001t0004g0196 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.259-4184T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044440 | ||||||
| chr17:44044712
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.259-4456A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044712 | ||||||
| chr17:44045000
|
G | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0214 | 3 | NA18947.hp2 NA18992.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.259-4744C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045000 | ||||||
| chr17:44045033
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.259-4777A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045033 | ||||||
| chr17:44045051
|
A | G | 33 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0034others(30): Show | 34 | HG00558.hp1 HG01106.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.259-4795T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045051 | ||||||
| chr17:44045067
|
G | A | 3 | a0001c0001t0002g0257a0001c0001t0002g0258a0001c0001t0002g0268 | 3 | NA19064.hp1 NA19080.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.259-4811C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045067 | ||||||
| chr17:44045185
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.259-4929C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045185 | ||||||
| chr17:44045263
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.259-5007A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045263 | ||||||
| chr17:44045300
|
A | G | 25 | a0001c0001t0001g0266a0001c0001t0002g0015a0001c0001t0002g0252others(22): Show | 25 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-5044T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045300 | ||||||
| chr17:44045304
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0210 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.259-5048C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045304 | ||||||
| chr17:44045593
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259-5337G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045593 | ||||||
| chr17:44045604
|
T | G | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259-5348A>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045604 | ||||||
| chr17:44045605
|
C | A | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259-5349G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045605 | ||||||
| chr17:44045744
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259-5488C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045744 | ||||||
| chr17:44045749
|
T | C | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-5493A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045749 | ||||||
| chr17:44045760
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-5504T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045760 | ||||||
| chr17:44045887
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.259-5631C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045887 | ||||||
| chr17:44045936
|
C | CT | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.259-5681dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045936 | ||||||
| chr17:44045936
|
C | CTT | 19 | a0001c0001t0001g0038a0001c0001t0001g0070a0001c0001t0001g0071others(16): Show | 20 | HG00438.hp2 HG01169.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.259-5682_259-5681d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045936 | ||||||
| chr17:44045936
|
C | CTTTTTTT others(1699): Show |
1 | a0001c0001t0001g0083 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.259-5681_259-5680i others(1708): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045936 | ||||||
| chr17:44045936
|
CT | C | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-5681delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045936 | ||||||
| chr17:44046227
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-5971C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046227 | ||||||
| chr17:44046569
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-6313A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046569 | ||||||
| chr17:44046613
|
A | G | 1 | a0001c0001t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-6357T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046613 | ||||||
| chr17:44046638
|
C | T | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.259-6382G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046638 | ||||||
| chr17:44046709
|
C | CA | 10 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0063others(7): Show | 10 | HG01169.hp1 HG01192.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-6454dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046709 | ||||||
| chr17:44046709
|
C | CAAAAAAA others(1699): Show |
1 | a0001c0001t0001g0124 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.259-6454_259-6453i others(1708): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046709 | ||||||
| chr17:44046742
|
GTTTTCTT others(5): Show |
G | 1 | a0001c0001t0011g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.259-6498_259-6487d others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046742 | ||||||
| chr17:44046747
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0237others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-6504_259-6492d others(15): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046747 | ||||||
| chr17:44046759
|
C | CT | 7 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0063others(4): Show | 7 | HG01978.hp2 HG02135.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-6504dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046759 | ||||||
| chr17:44046759
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259-6503G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046759 | ||||||
| chr17:44046759
|
CT | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.259-6504delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046759 | ||||||
| chr17:44046759
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0181others(2): Show | 5 | HG02523.hp1 HG02523.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-6515_259-6504d others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046759 | ||||||
| chr17:44046760
|
T | C | 3 | a0001c0001t0001g0149a0001c0001t0001g0173a0001c0001t0002g0088 | 3 | HG01123.hp1 NA18957.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259-6504A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046760 | ||||||
| chr17:44046808
|
G | A | 4 | a0001c0003t0002g0106a0001c0003t0002g0107a0001c0003t0002g0108others(1): Show | 4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-6552C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046808 | ||||||
| chr17:44046875
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 5 | HG01243.hp1 HG02280.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-6619G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046875 | ||||||
| chr17:44046939
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.259-6683G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046939 | ||||||
| chr17:44047010
|
G | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0237others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-6754C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047010 | ||||||
| chr17:44047061
|
A | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.259-6805T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047061 | ||||||
| chr17:44047448
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0125 | 2 | NA18957.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.259-7192G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047448 | ||||||
| chr17:44047742
|
G | GT | 26 | a0001c0001t0001g0055a0001c0001t0001g0116a0001c0001t0001g0133others(23): Show | 26 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-7487dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047742 | ||||||
| chr17:44047769
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.259-7513C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047769 | ||||||
| chr17:44047846
|
G | T | 1 | a0001c0001t0002g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.259-7590C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047846 | ||||||
| chr17:44047860
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(98): Show | 108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.259-7604T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047860 | ||||||
| chr17:44047879
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.259-7623C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047879 | ||||||
| chr17:44048018
|
A | AAC | 15 | a0001c0001t0001g0171a0001c0001t0001g0221a0001c0001t0001g0225others(12): Show | 15 | HG00741.hp1 HG01069.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-7764_259-7763d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
A | AACAC | 17 | a0001c0001t0001g0142a0001c0001t0001g0172a0001c0001t0001g0178others(14): Show | 17 | HG00280.hp2 HG01169.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.259-7766_259-7763d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
AAC | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 61 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.259-7764_259-7763d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
AACAC | A | 38 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0126others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.259-7766_259-7763d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
AACACAC | A | 16 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0001g0130others(13): Show | 16 | HG00558.hp1 HG00741.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.259-7768_259-7763d others(8): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
AACACACA others(1): Show |
A | 17 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0040others(14): Show | 19 | HG01243.hp1 HG02129.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.259-7770_259-7763d others(10): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
AACACACA others(3): Show |
A | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(56): Show | 67 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.259-7772_259-7763d others(12): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
AACACACA others(5): Show |
A | 20 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0090others(17): Show | 20 | HG00597.hp2 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.259-7774_259-7763d others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
AACACACA others(7): Show |
A | 10 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0161others(7): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-7776_259-7763d others(16): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048018
|
AACACACA others(9): Show |
A | 1 | a0001c0001t0002g0011 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259-7778_259-7763d others(18): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | ||||||
| chr17:44048231
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-7975G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048231 | ||||||
| chr17:44048280
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0003g0036 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.259-8024C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048280 | ||||||
| chr17:44048341
|
G | A | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-8085C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048341 | ||||||
| chr17:44048481
|
C | CA | 15 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0097others(12): Show | 15 | HG01109.hp2 HG01978.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-8226dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048481 | ||||||
| chr17:44048481
|
CA | C | 16 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0047others(13): Show | 16 | HG01123.hp1 HG01256.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-8226delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048481 | ||||||
| chr17:44048892
|
T | C | 2 | a0001c0001t0003g0147a0001c0001t0003g0148 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.259-8636A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048892 | ||||||
| chr17:44049010
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.259-8754C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049010 | ||||||
| chr17:44049065
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.259-8809G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049065 | ||||||
| chr17:44049123
|
G | A | 1 | a0001c0001t0008g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-8867C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049123 | ||||||
| chr17:44049141
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-8885T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049141 | ||||||
| chr17:44049191
|
A | C | 39 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0237others(36): Show | 39 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.259-8935T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049191 | ||||||
| chr17:44049220
|
C | T | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-8964G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049220 | ||||||
| chr17:44049221
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.259-8965C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049221 | ||||||
| chr17:44049233
|
C | A | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-8977G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049233 | ||||||
| chr17:44049312
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.259-9056A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049312 | ||||||
| chr17:44049370
|
T | C | 1 | a0001c0001t0002g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.259-9114A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049370 | ||||||
| chr17:44049475
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0233 | 2 | HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.259-9219C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049475 | ||||||
| chr17:44049524
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.259-9268G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049524 | ||||||
| chr17:44049577
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.259-9321T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049577 | ||||||
| chr17:44049648
|
G | A | 4 | a0001c0003t0002g0106a0001c0003t0002g0107a0001c0003t0002g0108others(1): Show | 4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-9392C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049648 | ||||||
| chr17:44049726
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.259-9470A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049726 | ||||||
| chr17:44049758
|
G | A | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.259-9502C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049758 | ||||||
| chr17:44049960
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.259-9704C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049960 | ||||||
| chr17:44049976
|
C | G | 3 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0148 | 3 | HG01106.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.259-9720G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049976 | ||||||
| chr17:44050202
|
C | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 91 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.259-9946G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050202 | ||||||
| chr17:44050275
|
A | AT | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(82): Show | 93 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.259-10020dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050275 | ||||||
| chr17:44050333
|
CT | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 99 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.259-10078delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050333 | ||||||
| chr17:44050516
|
A | AT | 12 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0095others(9): Show | 13 | HG01346.hp2 HG02145.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-10261dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050516 | ||||||
| chr17:44050667
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-10411G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050667 | ||||||
| chr17:44050706
|
A | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.259-10450T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050706 | ||||||
| chr17:44050719
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0095 | 3 | NA18972.hp2 NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.259-10463G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050719 | ||||||
| chr17:44050904
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.259-10648C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050904 | ||||||
| chr17:44050969
|
A | T | 1 | a0001c0001t0008g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-10713T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050969 | ||||||
| chr17:44051033
|
G | C | 1 | a0001c0001t0001g0266 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.259-10777C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051033 | ||||||
| chr17:44051040
|
G | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0063others(3): Show | 6 | HG01192.hp1 HG01934.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-10784C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051040 | ||||||
| chr17:44051187
|
A | T | 1 | a0001c0001t0002g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-10931T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051187 | ||||||
| chr17:44051389
|
C | CA | 19 | a0001c0001t0001g0016a0001c0001t0002g0011a0001c0001t0002g0246others(16): Show | 20 | HG01169.hp2 HG01256.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.259-11134dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | ||||||
| chr17:44051389
|
C | CAA | 17 | a0001c0001t0001g0266a0001c0001t0002g0254a0001c0001t0002g0255others(14): Show | 17 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.259-11135_259-1113 others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | ||||||
| chr17:44051389
|
C | CAAA | 9 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0002g0111others(6): Show | 9 | HG00738.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-11136_259-1113 others(7): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | ||||||
| chr17:44051389
|
CAAAAAAA others(1): Show |
C | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(82): Show | 94 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.259-11141_259-1113 others(12): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | ||||||
| chr17:44051389
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0168a0001c0001t0001g0215a0001c0001t0001g0218 | 3 | HG00597.hp1 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.259-11143_259-1113 others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | ||||||
| chr17:44051389
|
CAAAAAAA others(4): Show |
C | 88 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.259-11144_259-1113 others(15): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | ||||||
| chr17:44051389
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0173a0001c0001t0002g0037a0001c0001t0005g0104 | 3 | HG03139.hp1 NA18957.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.259-11145_259-1113 others(16): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | ||||||
| chr17:44051389
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0036 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259-11146_259-1113 others(17): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | ||||||
| chr17:44051527
|
T | C | 22 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(19): Show | 22 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.259-11271A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051527 | ||||||
| chr17:44051791
|
T | C | 3 | a0001c0001t0008g0012a0001c0001t0008g0278a0001c0001t0008g0279 | 4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-11535A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051791 | ||||||
| chr17:44051818
|
A | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG02559.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.259-11562T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051818 | ||||||
| chr17:44051826
|
G | A | 22 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(19): Show | 22 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.259-11570C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051826 | ||||||
| chr17:44051840
|
G | A | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-11584C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051840 | ||||||
| chr17:44051879
|
G | A | 2 | a0001c0001t0003g0022a0001c0001t0003g0157 | 2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.259-11623C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051879 | ||||||
| chr17:44051880
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11624C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051880 | ||||||
| chr17:44051895
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11639C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051895 | ||||||
| chr17:44051896
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11640A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051896 | ||||||
| chr17:44051898
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11642T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051898 | ||||||
| chr17:44051899
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11643G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051899 | ||||||
| chr17:44051910
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11654G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051910 | ||||||
| chr17:44051911
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11655G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051911 | ||||||
| chr17:44051999
|
C | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.259-11743G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051999 | ||||||
| chr17:44052115
|
T | G | 1 | a0001c0001t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.258+11686A>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052115 | ||||||
| chr17:44052190
|
C | A | 1 | a0001c0001t0008g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258+11611G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052190 | ||||||
| chr17:44052230
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.258+11571A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052230 | ||||||
| chr17:44052257
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+11544G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052257 | ||||||
| chr17:44052260
|
C | CA | 14 | a0001c0001t0001g0030a0001c0001t0001g0061a0001c0001t0001g0098others(11): Show | 14 | HG00558.hp2 HG01099.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+11540dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052260 | ||||||
| chr17:44052270
|
A | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0062 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.258+11531T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052270 | ||||||
| chr17:44052489
|
T | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0237others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+11312A>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052489 | ||||||
| chr17:44052556
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+11245G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052556 | ||||||
| chr17:44052557
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 99 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.258+11244C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052557 | ||||||
| chr17:44052642
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.258+11159G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052642 | ||||||
| chr17:44052766
|
A | T | 1 | a0001c0001t0002g0256 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.258+11035T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052766 | ||||||
| chr17:44052817
|
AT | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG01243.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+10983delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052817 | ||||||
| chr17:44052850
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0011g0239 | 3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+10951T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052850 | ||||||
| chr17:44053183
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.258+10618C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053183 | ||||||
| chr17:44053215
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0011g0239 | 3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+10586T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053215 | ||||||
| chr17:44053234
|
A | G | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+10567T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053234 | ||||||
| chr17:44053244
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.258+10557A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053244 | ||||||
| chr17:44053293
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.258+10508C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053293 | ||||||
| chr17:44053575
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0241a0001c0001t0002g0137 | 3 | HG02055.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.258+10226C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053575 | ||||||
| chr17:44053695
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.258+10106A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053695 | ||||||
| chr17:44053724
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.258+10077C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053724 | ||||||
| chr17:44054196
|
T | C | 1 | a0001c0001t0003g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.258+9605A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054196 | ||||||
| chr17:44054511
|
G | A | 1 | a0001c0001t0008g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258+9290C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054511 | ||||||
| chr17:44054822
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0112 | 3 | HG00558.hp2 NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.258+8979G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054822 | ||||||
| chr17:44054909
|
G | C | 1 | a0001c0001t0001g0095 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.258+8892C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054909 | ||||||
| chr17:44054910
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.258+8891G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054910 | ||||||
| chr17:44055000
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0130 | 2 | HG00558.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.258+8801C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055000 | ||||||
| chr17:44055385
|
G | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(78): Show | 89 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.258+8416C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055385 | ||||||
| chr17:44055507
|
C | A | 1 | a0001c0001t0001g0095 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.258+8294G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055507 | ||||||
| chr17:44055507
|
C | CA | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(91): Show | 103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.258+8293dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055507 | ||||||
| chr17:44055507
|
C | CAA | 10 | a0001c0001t0001g0056a0001c0001t0001g0086a0001c0001t0001g0090others(7): Show | 10 | HG02559.hp1 HG03098.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+8292_258+8293d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055507 | ||||||
| chr17:44055507
|
CA | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 6 | HG02109.hp2 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+8293delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055507 | ||||||
| chr17:44055672
|
C | T | 23 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(20): Show | 23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+8129G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055672 | ||||||
| chr17:44055680
|
T | TATATATA others(26): Show |
1 | a0001c0001t0006g0156 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.258+8088_258+8120d others(35): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055680 | ||||||
| chr17:44055682
|
T | TATATATA others(15): Show |
2 | a0001c0001t0002g0015a0001c0001t0002g0273 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+8097_258+8118d others(24): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055682 | ||||||
| chr17:44055691
|
A | AAT | 3 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0002g0145 | 3 | HG03516.hp2 NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.258+8108_258+8109d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055691 | ||||||
| chr17:44055721
|
TA | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 10 | HG00558.hp2 HG00673.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+8079delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055721 | ||||||
| chr17:44055978
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.258+7823C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055978 | ||||||
| chr17:44055992
|
G | A | 3 | a0001c0001t0008g0012a0001c0001t0008g0278a0001c0001t0008g0279 | 4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+7809C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055992 | ||||||
| chr17:44056030
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.258+7771T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056030 | ||||||
| chr17:44056100
|
T | G | 2 | a0002c0002t0003g0020a0002c0002t0003g0021 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.258+7701A>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056100 | ||||||
| chr17:44056219
|
C | T | 1 | a0001c0001t0014g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.258+7582G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056219 | ||||||
| chr17:44056295
|
C | CA | 9 | a0001c0001t0001g0030a0001c0001t0001g0116a0001c0001t0001g0125others(6): Show | 9 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+7505dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056295 | ||||||
| chr17:44056449
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.258+7352A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056449 | ||||||
| chr17:44056573
|
G | A | 3 | a0001c0001t0008g0012a0001c0001t0008g0278a0001c0001t0008g0279 | 4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+7228C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056573 | ||||||
| chr17:44056663
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.258+7138T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056663 | ||||||
| chr17:44056700
|
G | GA | 9 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0172others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+7100dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056700 | ||||||
| chr17:44056701
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.258+7100T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056701 | ||||||
| chr17:44056703
|
A | G | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+7098T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056703 | ||||||
| chr17:44056864
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0089a0001c0001t0001g0099 | 3 | NA18960.hp1 NA18989.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.258+6937C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056864 | ||||||
| chr17:44057156
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.258+6645A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057156 | ||||||
| chr17:44057157
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.258+6644G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057157 | ||||||
| chr17:44057181
|
G | A | 4 | a0001c0003t0002g0106a0001c0003t0002g0107a0001c0003t0002g0108others(1): Show | 4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+6620C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057181 | ||||||
| chr17:44057391
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.258+6410C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057391 | ||||||
| chr17:44057437
|
C | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0237others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+6364G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057437 | ||||||
| chr17:44057499
|
C | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 92 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.258+6302G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057499 | ||||||
| chr17:44057607
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.258+6194T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057607 | ||||||
| chr17:44057715
|
C | A | 4 | a0002c0002t0003g0019a0002c0002t0003g0020a0002c0002t0003g0021others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+6086G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057715 | ||||||
| chr17:44057727
|
A | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.258+6074T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057727 | ||||||
| chr17:44057728
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.258+6073A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057728 | ||||||
| chr17:44057734
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.258+6067C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057734 | ||||||
| chr17:44057943
|
T | TA | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(126): Show | 136 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.258+5857dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057943 | ||||||
| chr17:44058036
|
A | C | 1 | a0001c0001t0002g0111 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258+5765T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058036 | ||||||
| chr17:44058110
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+5691C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058110 | ||||||
| chr17:44058163
|
G | C | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+5638C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058163 | ||||||
| chr17:44058192
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+5609C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058192 | ||||||
| chr17:44058251
|
AAAT | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+5547_258+5549d others(5): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058251 | ||||||
| chr17:44058292
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+5509T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058292 | ||||||
| chr17:44058490
|
C | G | 5 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(2): Show | 5 | HG02080.hp2 HG02523.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+5311G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058490 | ||||||
| chr17:44058559
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA18943.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.258+5242C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058559 | ||||||
| chr17:44058701
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.258+5100C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058701 | ||||||
| chr17:44058817
|
A | C | 3 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0115 | 3 | HG02965.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.258+4984T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058817 | ||||||
| chr17:44058823
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0011g0239 | 3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+4978T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058823 | ||||||
| chr17:44058837
|
A | G | 1 | a0001c0001t0003g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258+4964T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058837 | ||||||
| chr17:44058838
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0011g0239 | 3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+4963T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058838 | ||||||
| chr17:44058894
|
G | C | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+4907C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058894 | ||||||
| chr17:44058926
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.258+4875G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058926 | ||||||
| chr17:44058985
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.258+4816T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058985 | ||||||
| chr17:44059066
|
T | C | 1 | a0001c0001t0016g0277 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.258+4735A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059066 | ||||||
| chr17:44059102
|
G | A | 2 | a0001c0001t0003g0022a0001c0001t0003g0157 | 2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.258+4699C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059102 | ||||||
| chr17:44059207
|
C | T | 23 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(20): Show | 23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+4594G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059207 | ||||||
| chr17:44059378
|
C | A | 3 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0115 | 3 | HG02965.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.258+4423G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059378 | ||||||
| chr17:44059418
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.258+4383T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059418 | ||||||
| chr17:44059493
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.258+4308C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059493 | ||||||
| chr17:44059658
|
T | C | 1 | a0001c0001t0008g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.258+4143A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059658 | ||||||
| chr17:44059744
|
AAGCCCTT others(9): Show |
A | 4 | a0001c0003t0002g0106a0001c0003t0002g0107a0001c0003t0002g0108others(1): Show | 4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+4041_258+4056d others(18): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059744 | ||||||
| chr17:44059837
|
C | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0011g0239 | 3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+3964G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059837 | ||||||
| chr17:44059939
|
C | T | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+3862G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059939 | ||||||
| chr17:44059979
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+3822T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059979 | ||||||
| chr17:44060090
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.258+3711C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44060090 | ||||||
| chr17:44060365
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.258+3436T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44060365 | ||||||
| chr17:44060744
|
C | G | 2 | a0001c0001t0007g0026a0001c0001t0007g0027 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.258+3057G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44060744 | ||||||
| chr17:44060922
|
CCTCT | C | 23 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(20): Show | 23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+2875_258+2878d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44060922 | ||||||
| chr17:44061024
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.258+2777G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061024 | ||||||
| chr17:44061070
|
C | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(102): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.258+2731G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061070 | ||||||
| chr17:44061105
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.258+2696C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061105 | ||||||
| chr17:44061241
|
C | T | 5 | a0001c0001t0007g0026a0001c0001t0007g0027a0001c0001t0007g0028others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+2560G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061241 | ||||||
| chr17:44061317
|
CA | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.258+2483delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061317 | ||||||
| chr17:44061506
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.258+2295A>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061506 | ||||||
| chr17:44061542
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 5 | HG01243.hp1 HG02280.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+2259T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061542 | ||||||
| chr17:44061875
|
G | A | 7 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(4): Show | 7 | HG02040.hp1 NA18944.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+1926C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061875 | ||||||
| chr17:44061889
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.258+1912G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061889 | ||||||
| chr17:44061990
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(100): Show | 109 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.258+1811C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061990 | ||||||
| chr17:44062091
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.258+1710C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062091 | ||||||
| chr17:44062095
|
G | A | 23 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(20): Show | 23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+1706C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062095 | ||||||
| chr17:44062108
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0231 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.258+1693C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062108 | ||||||
| chr17:44062200
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00597.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.258+1601G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062200 | ||||||
| chr17:44062221
|
C | CA | 103 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(100): Show | 109 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.258+1579dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062221 | ||||||
| chr17:44062221
|
C | CAA | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG00639.hp2 HG01175.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+1578_258+1579d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062221 | ||||||
| chr17:44062221
|
CA | C | 14 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(11): Show | 14 | HG01243.hp2 HG01256.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+1579delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062221 | ||||||
| chr17:44062286
|
TA | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 99 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.258+1514delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062286 | ||||||
| chr17:44062412
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.258+1389C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062412 | ||||||
| chr17:44062609
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.258+1192C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062609 | ||||||
| chr17:44062770
|
C | A | 1 | a0001c0001t0014g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.258+1031G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062770 | ||||||
| chr17:44062860
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.258+941A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062860 | ||||||
| chr17:44062890
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.258+911C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062890 | ||||||
| chr17:44062898
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(100): Show | 109 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.258+903G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062898 | ||||||
| chr17:44062971
|
G | A | 9 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0237others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+830C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062971 | ||||||
| chr17:44063025
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18962.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.258+776G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44063025 | ||||||
| chr17:44063220
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+581G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44063220 | ||||||
| chr17:44063254
|
G | C | 3 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0002g0275 | 3 | HG01081.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.258+547C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44063254 | ||||||
| chr17:44063448
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.258+353C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44063448 | ||||||
| chr17:44064004
|
T | C | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125-70A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064004 | ||||||
| chr17:44064254
|
ACT | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.125-322_125-321del others(2): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064254 | ||||||
| chr17:44064270
|
C | G | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0138others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-336G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064270 | ||||||
| chr17:44064286
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.125-352G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064286 | ||||||
| chr17:44064570
|
C | CA | 9 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0237others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-637dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064570 | ||||||
| chr17:44064732
|
C | CA | 6 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | HG00621.hp1 HG02135.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-799dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064732 | ||||||
| chr17:44064732
|
CA | C | 11 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0034others(8): Show | 11 | HG01069.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.125-799delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064732 | ||||||
| chr17:44064815
|
G | T | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-881C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064815 | ||||||
| chr17:44064865
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.125-931C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064865 | ||||||
| chr17:44065145
|
C | CA | 16 | a0001c0001t0001g0016a0001c0001t0001g0116a0001c0001t0001g0117others(13): Show | 16 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.125-1212dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065145 | ||||||
| chr17:44065270
|
T | TA | 6 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0005g0244others(3): Show | 7 | HG01975.hp1 HG02723.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+1193dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065270 | ||||||
| chr17:44065378
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.124+1086A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065378 | ||||||
| chr17:44065439
|
TA | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(106): Show | 119 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.124+1024delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065439 | ||||||
| chr17:44065439
|
TAA | T | 36 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0266others(33): Show | 37 | HG00099.hp1 HG00558.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+1023_124+1024d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065439 | ||||||
| chr17:44065439
|
TAAA | T | 12 | a0001c0001t0002g0252a0001c0001t0002g0254a0001c0001t0003g0004others(9): Show | 13 | HG00741.hp1 HG01109.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+1022_124+1024d others(5): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065439 | ||||||
| chr17:44065567
|
T | C | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+897A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065567 | ||||||
| chr17:44065758
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.124+706T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065758 | ||||||
| chr17:44065810
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.124+654G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065810 | ||||||
| chr17:44065864
|
C | A | 7 | a0001c0001t0002g0011a0001c0001t0002g0246a0001c0001t0002g0247others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+600G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065864 | ||||||
| chr17:44065884
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.124+580G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065884 | ||||||
| chr17:44065888
|
T | C | 24 | a0001c0001t0001g0266a0001c0001t0002g0252a0001c0001t0002g0254others(21): Show | 24 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.124+576A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065888 | ||||||
| chr17:44066295
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.124+169G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44066295 |