Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 389421 |
|---|---|
| ensemblid | ENSG00000187772.8 |
| hgncid | 32207 |
| symbol | LIN28B |
| name | lin-28 homolog B |
| refseq_nuc | NM_001004317.4 |
| refseq_prot | NP_001004317.1 |
| ensembl_nuc | ENST00000345080.5 |
| ensembl_prot | ENSP00000344401.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 104957107 |
| end | 105083332 |
| strand | + |
| ver | v1.2 |
| region | chr6:104957107-105083332 |
| region5000 | chr6:104952107-105088332 |
| regionname0 | LIN28B_chr6_104957107_105083332 |
| regionname5000 | LIN28B_chr6_104952107_105088332 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 250 | 277 | 83 | 38 | 106 | 16 | 32 | 88 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0002 | 0/0 | 250 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 753 | 276 | 82 | 38 | 106 | 16 | 32 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| c0002 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| c0003 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4694 | 76 | 15 | 11 | 32 | 7 | 11 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0002 | 1/0 | 4694 | 64 | 19 | 7 | 27 | 5 | 5 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0003 | 0/0 | 4692 | 55 | 1 | 10 | 35 | 1 | 8 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0004 | 0/1 | 4694 | 28 | 15 | 4 | 0 | 3 | 5 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0005 | 0/0 | 4694 | 12 | 11 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0006 | 0/0 | 4694 | 7 | 7 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0007 | 0/0 | 4694 | 5 | 5 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0008 | 0/0 | 4694 | 3 | 0 | 0 | 3 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0009 | 0/0 | 4694 | 3 | 3 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0010 | 0/0 | 4694 | 3 | 0 | 3 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0011 | 0/0 | 4692 | 3 | 0 | 0 | 3 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0012 | 0/0 | 4694 | 2 | 0 | 1 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0013 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0014 | 0/0 | 4694 | 2 | 2 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0015 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0016 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0017 | 0/0 | 4694 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0018 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0019 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0020 | 0/0 | 4694 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0021 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0022 | 0/0 | 4692 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0023 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0024 | 0/0 | 4694 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0025 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0026 | 0/0 | 4694 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| t0027 | 0/0 | 4694 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 753 | 276 | 82 | 38 | 106 | 16 | 32 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0002 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0002c0003 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5446 | 76 | 15 | 11 | 32 | 7 | 11 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0002 | 1/0 | 5446 | 63 | 18 | 7 | 27 | 5 | 5 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0003 | 0/0 | 5444 | 55 | 1 | 10 | 35 | 1 | 8 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0004 | 0/1 | 5446 | 28 | 15 | 4 | 0 | 3 | 5 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0005 | 0/0 | 5446 | 12 | 11 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0006 | 0/0 | 5446 | 7 | 7 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0007 | 0/0 | 5446 | 4 | 4 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0008 | 0/0 | 5446 | 3 | 0 | 0 | 3 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0009 | 0/0 | 5446 | 3 | 3 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0010 | 0/0 | 5446 | 3 | 0 | 3 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0011 | 0/0 | 5444 | 3 | 0 | 0 | 3 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0012 | 0/0 | 5446 | 2 | 0 | 1 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0013 | 0/0 | 5446 | 2 | 2 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0014 | 0/0 | 5446 | 2 | 2 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0015 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0016 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0017 | 0/0 | 5446 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0018 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0019 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0020 | 0/0 | 5446 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0021 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0022 | 0/0 | 5444 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0023 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0024 | 0/0 | 5446 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0025 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0026 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0001t0027 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0001c0002t0007 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| a0002c0003t0002 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | copy fasta | chr6 | 104952107 | 105088332 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0001 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0010g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0010g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0011g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0012g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0012g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0014g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0016g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0017g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0018g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0019g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0020g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0021g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0022g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0023g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0024g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0025g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0026g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0001t0027g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0001c0002t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| a0002c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | GBR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0249 | EUR | FIN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00423 | hp2 | a0001 | c0001 | t0022 | g0085 | EAS | CHS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0198 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0240 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0120 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0142 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01255 | hp2 | a0001 | c0001 | t0012 | g0234 | AMR | CLM | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | CLM | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0121 | AMR | CLM | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0236 | EUR | IBS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0099 | EUR | IBS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0248 | EUR | IBS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0247 | EUR | IBS | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0056 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02074 | hp2 | a0001 | c0001 | t0011 | g0081 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | CDX | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0175 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02630 | hp2 | a0001 | c0001 | t0027 | g0049 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02723 | hp1 | a0001 | c0001 | t0016 | g0011 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02895 | hp1 | a0001 | c0001 | t0023 | g0050 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0171 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0059 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03225 | hp2 | a0001 | c0001 | t0025 | g0112 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03516 | hp2 | a0001 | c0002 | t0007 | g0005 | AFR | ESN | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03654 | hp2 | a0001 | c0001 | t0024 | g0156 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03669 | hp1 | a0001 | c0001 | t0012 | g0233 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03704 | hp1 | a0001 | c0001 | t0017 | g0176 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | BEB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | STU | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | YRI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0058 | AFR | YRI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | YRI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | YRI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18948 | hp2 | a0001 | c0001 | t0008 | g0132 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18962 | hp2 | a0001 | c0001 | t0018 | g0190 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18963 | hp1 | a0001 | c0001 | t0019 | g0202 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18989 | hp1 | a0001 | c0001 | t0011 | g0076 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19004 | hp2 | a0001 | c0001 | t0015 | g0162 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19009 | hp1 | a0001 | c0001 | t0026 | g0261 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19009 | hp2 | a0001 | c0001 | t0008 | g0147 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19012 | hp2 | a0001 | c0001 | t0008 | g0157 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | LWK | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | LWK | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | LWK | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0089 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19091 | hp2 | a0001 | c0001 | t0021 | g0230 | EAS | JPT | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | YRI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ASW | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | ASW | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | TSI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0242 | EUR | TSI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | TSI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | GIH | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | GIH | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | MSL | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | USA | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | USA | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0237 | AFR | USA | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0235 | AFR | LWK | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0001 | REF | REF | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0272 | REF | REF | LIN28B_chr6_104952107_105088332 | LIN28B | chr6 | 104952107 | 105088332 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:105078457
|
A | C | 1 | a0002 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.427A>C | p.Ser143Arg | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 571/5446 | 427/753 | 143/250 | chr6 | 105078457 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:105078621
|
C | T | 1 | a0001c0002 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.591C>T | p.Gly197Gly | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 735/5446 | 591/753 | 197/250 | chr6 | 105078621 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:104957240
|
C | T | 1 | a0001c0001t0027 | 1 | HG02630.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 1/4 | chr6 | 104957240 | ||||||
| chr6:105078899
|
G | T | 1 | a0001c0001t0011 | 3 | HG02074.hp2 NA18989.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*116G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 116 | chr6 | 105078899 | |||||
| chr6:105078981
|
A | G | 1 | a0001c0001t0026 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 198 | chr6 | 105078981 | |||||
| chr6:105079229
|
A | G | 1 | a0001c0001t0025 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 446 | chr6 | 105079229 | |||||
| chr6:105079290
|
T | C | 1 | a0001c0001t0008 | 3 | NA18948.hp2 NA19009.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*507T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 507 | chr6 | 105079290 | |||||
| chr6:105079302
|
C | T | 1 | a0001c0001t0006 | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*519C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 519 | chr6 | 105079302 | |||||
| chr6:105079498
|
T | C | 1 | a0001c0001t0009 | 3 | HG02615.hp2 HG02976.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*715T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 715 | chr6 | 105079498 | |||||
| chr6:105080101
|
G | A | 1 | a0001c0001t0015 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1318G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 1318 | chr6 | 105080101 | |||||
| chr6:105080185
|
T | C | 1 | a0001c0001t0016 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 1402 | chr6 | 105080185 | |||||
| chr6:105080213
|
T | A | 8 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(5): Show | 88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1430T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 1430 | chr6 | 105080213 | |||||
| chr6:105080245
|
T | C | 1 | a0001c0001t0005 | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1462T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 1462 | chr6 | 105080245 | |||||
| chr6:105080321
|
T | G | 1 | a0001c0001t0017 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1538T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 1538 | chr6 | 105080321 | |||||
| chr6:105081277
|
C | T | 1 | a0001c0001t0024 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2494C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 2494 | chr6 | 105081277 | |||||
| chr6:105081299
|
T | C | 1 | a0001c0001t0005 | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2516T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 2516 | chr6 | 105081299 | |||||
| chr6:105081317
|
T | A | 1 | a0001c0001t0019 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2534T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 2534 | chr6 | 105081317 | |||||
| chr6:105081452
|
A | G | 2 | a0001c0001t0007a0001c0002t0007 | 5 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2669A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 2669 | chr6 | 105081452 | |||||
| chr6:105081477
|
T | A | 1 | a0001c0001t0024 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2694T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 2694 | chr6 | 105081477 | |||||
| chr6:105081612
|
C | G | 1 | a0001c0001t0010 | 3 | HG00735.hp2 HG01243.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2829C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 2829 | chr6 | 105081612 | |||||
| chr6:105081636
|
T | C | 1 | a0001c0001t0013 | 2 | HG02055.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2853T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 2853 | chr6 | 105081636 | |||||
| chr6:105081759
|
G | C | 1 | a0001c0001t0012 | 2 | HG01255.hp2 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2976G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 2976 | chr6 | 105081759 | |||||
| chr6:105081799
|
C | T | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3016C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 3016 | chr6 | 105081799 | |||||
| chr6:105081862
|
C | G | 1 | a0001c0001t0023 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3079C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 3079 | chr6 | 105081862 | |||||
| chr6:105081910
|
A | C | 4 | a0001c0001t0003a0001c0001t0011a0001c0001t0018others(1): Show | 60 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3127A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 3127 | chr6 | 105081910 | |||||
| chr6:105082089
|
T | A | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*3306T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 3306 | chr6 | 105082089 | |||||
| chr6:105082295
|
T | A | 1 | a0001c0001t0020 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3512T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 3512 | chr6 | 105082295 | |||||
| chr6:105082332
|
C | T | 1 | a0001c0001t0021 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3549C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 3549 | chr6 | 105082332 | |||||
| chr6:105082373
|
G | A | 1 | a0001c0001t0006 | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3590G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 3590 | chr6 | 105082373 | |||||
| chr6:105082695
|
T | G | 1 | a0001c0001t0022 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3912T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 3912 | chr6 | 105082695 | |||||
| chr6:105083119
|
GTA | G | 3 | a0001c0001t0003a0001c0001t0011a0001c0001t0022 | 59 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*4338_*4339delAT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 4/4 | 4338 | INFO_REALIGN_3_PRIME | chr6 | 105083119 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:104957345
|
T | TC | 271 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.10+92dupC | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 104957345 | |||||
| chr6:104958025
|
A | AT | 15 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0271others(12): Show | 15 | HG00558.hp1 HG02135.hp2 NA18939.hp2 others(12): Show |
intron_variant | MODIFIER | c.11-62dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 104958025 | |||||
| chr6:104958068
|
A | C | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.11-31A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 1/3 | chr6 | 104958068 | ||||||
| chr6:104958399
|
A | C | 22 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.198+113A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104958399 | ||||||
| chr6:104958438
|
A | T | 2 | a0001c0001t0012g0233a0001c0001t0012g0234 | 2 | HG01255.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.198+152A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104958438 | ||||||
| chr6:104958449
|
C | T | 18 | a0001c0001t0001g0241a0001c0001t0002g0239a0001c0001t0002g0242others(15): Show | 19 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+163C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104958449 | ||||||
| chr6:104958886
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.198+600T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104958886 | ||||||
| chr6:104959143
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0002g0228a0001c0001t0002g0229others(2): Show | 5 | NA18949.hp1 NA18952.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+857C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104959143 | ||||||
| chr6:104959243
|
A | G | 1 | a0001c0001t0009g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.198+957A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104959243 | ||||||
| chr6:104959328
|
A | C | 1 | a0001c0001t0004g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.198+1042A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104959328 | ||||||
| chr6:104959787
|
A | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0091a0001c0001t0001g0098others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.198+1501A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104959787 | ||||||
| chr6:104959787
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.198+1501A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104959787 | ||||||
| chr6:104959885
|
G | A | 5 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+1599G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104959885 | ||||||
| chr6:104959902
|
T | A | 2 | a0001c0001t0003g0065a0001c0001t0003g0066 | 2 | HG01928.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.198+1616T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104959902 | ||||||
| chr6:104960027
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.198+1741C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104960027 | ||||||
| chr6:104960124
|
A | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.198+1838A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104960124 | ||||||
| chr6:104960445
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.198+2159G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104960445 | ||||||
| chr6:104960554
|
T | G | 1 | a0001c0001t0003g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.198+2268T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104960554 | ||||||
| chr6:104960574
|
T | G | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+2288T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104960574 | ||||||
| chr6:104960597
|
C | T | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(1): Show | 4 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+2311C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104960597 | ||||||
| chr6:104961091
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0111others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.198+2805T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104961091 | ||||||
| chr6:104961217
|
T | G | 2 | a0001c0001t0003g0269a0001c0001t0003g0270 | 2 | NA18939.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.198+2931T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104961217 | ||||||
| chr6:104961458
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0005g0019 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.198+3172T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104961458 | ||||||
| chr6:104961549
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | NA18959.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.198+3263C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104961549 | ||||||
| chr6:104961689
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.198+3403C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104961689 | ||||||
| chr6:104962099
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198+3813A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104962099 | ||||||
| chr6:104962162
|
T | C | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+3876T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104962162 | ||||||
| chr6:104962173
|
C | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.198+3887C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104962173 | ||||||
| chr6:104962303
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.198+4017G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104962303 | ||||||
| chr6:104962630
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.198+4344A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104962630 | ||||||
| chr6:104962722
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.198+4436G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104962722 | ||||||
| chr6:104963203
|
C | T | 11 | a0001c0001t0001g0258a0001c0001t0002g0259a0001c0001t0002g0260others(8): Show | 11 | HG02135.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.198+4917C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104963203 | ||||||
| chr6:104963334
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.198+5048C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104963334 | ||||||
| chr6:104963425
|
C | T | 1 | a0001c0001t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198+5139C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104963425 | ||||||
| chr6:104963427
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.198+5141T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104963427 | ||||||
| chr6:104963800
|
A | G | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0025g0112 | 3 | HG02572.hp1 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.198+5514A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104963800 | ||||||
| chr6:104963894
|
A | G | 23 | a0001c0001t0001g0207a0001c0001t0001g0216a0001c0001t0002g0199others(20): Show | 23 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+5608A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104963894 | ||||||
| chr6:104964147
|
T | G | 1 | a0001c0001t0001g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.198+5861T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104964147 | ||||||
| chr6:104964148
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+5862C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104964148 | ||||||
| chr6:104964256
|
A | C | 2 | a0001c0001t0004g0113a0001c0001t0004g0114 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.198+5970A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104964256 | ||||||
| chr6:104964579
|
C | CAATGCAT | 3 | a0001c0001t0001g0197a0001c0001t0003g0196a0001c0001t0010g0198 | 3 | HG00735.hp2 HG01106.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.198+6296_198+6302d others(9): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104964579 | |||||
| chr6:104964642
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.198+6356A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104964642 | ||||||
| chr6:104964829
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.198+6543T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104964829 | ||||||
| chr6:104965057
|
A | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0111others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.198+6771A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104965057 | ||||||
| chr6:104965243
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.198+6957C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104965243 | ||||||
| chr6:104965495
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.198+7209T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104965495 | ||||||
| chr6:104966373
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.198+8087T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104966373 | ||||||
| chr6:104966374
|
A | T | 13 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0186others(10): Show | 13 | HG01258.hp1 HG01943.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+8088A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104966374 | ||||||
| chr6:104966484
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.198+8198A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104966484 | ||||||
| chr6:104966491
|
T | C | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+8205T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104966491 | ||||||
| chr6:104966619
|
A | AT | 19 | a0001c0001t0001g0116a0001c0001t0001g0177a0001c0001t0001g0178others(16): Show | 19 | HG00099.hp2 HG01106.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+8353dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104966619 | |||||
| chr6:104966619
|
AT | A | 24 | a0001c0001t0001g0181a0001c0001t0001g0238a0001c0001t0001g0241others(21): Show | 25 | HG00323.hp2 HG00558.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.198+8353delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104966619 | |||||
| chr6:104966782
|
C | T | 8 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+8496C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104966782 | ||||||
| chr6:104966882
|
A | G | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+8596A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104966882 | ||||||
| chr6:104967056
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.198+8770C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967056 | ||||||
| chr6:104967075
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.198+8789G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967075 | ||||||
| chr6:104967086
|
GT | G | 5 | a0001c0001t0001g0111a0001c0001t0001g0256a0001c0001t0004g0113others(2): Show | 5 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+8809delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104967086 | |||||
| chr6:104967334
|
C | CT | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.198+9051dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104967334 | |||||
| chr6:104967349
|
G | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | NA18960.hp2 NA18961.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.198+9063G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967349 | ||||||
| chr6:104967353
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.198+9067G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967353 | ||||||
| chr6:104967529
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.198+9243C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967529 | ||||||
| chr6:104967576
|
CA | C | 229 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.198+9313delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104967576 | |||||
| chr6:104967576
|
CAA | C | 13 | a0001c0001t0001g0098a0001c0001t0001g0167a0001c0001t0001g0168others(10): Show | 13 | HG01069.hp2 HG01167.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+9312_198+9313d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104967576 | |||||
| chr6:104967596
|
A | G | 9 | a0001c0001t0001g0223a0001c0001t0002g0110a0001c0001t0003g0100others(6): Show | 9 | HG00642.hp2 NA18947.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+9310A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967596 | ||||||
| chr6:104967614
|
T | C | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198+9328T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967614 | ||||||
| chr6:104967658
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+9372A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967658 | ||||||
| chr6:104967674
|
A | AATT | 26 | a0001c0001t0001g0111a0001c0001t0001g0238a0001c0001t0001g0241others(23): Show | 27 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.198+9407_198+9409d others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104967674 | |||||
| chr6:104967798
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+9512C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967798 | ||||||
| chr6:104967823
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.198+9537C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104967823 | ||||||
| chr6:104968036
|
G | A | 27 | a0001c0001t0001g0111a0001c0001t0001g0238a0001c0001t0001g0241others(24): Show | 28 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.198+9750G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968036 | ||||||
| chr6:104968073
|
G | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.198+9787G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968073 | ||||||
| chr6:104968086
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.198+9800G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968086 | ||||||
| chr6:104968207
|
A | G | 1 | a0001c0001t0002g0166 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.198+9921A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968207 | ||||||
| chr6:104968247
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+9961T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968247 | ||||||
| chr6:104968249
|
T | G | 1 | a0001c0001t0003g0070 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.198+9963T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968249 | ||||||
| chr6:104968264
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0004g0053 | 3 | HG00642.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.198+9978G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968264 | ||||||
| chr6:104968488
|
T | A | 1 | a0001c0001t0002g0199 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.198+10202T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968488 | ||||||
| chr6:104968686
|
A | T | 1 | a0001c0001t0014g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.198+10400A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104968686 | ||||||
| chr6:104969119
|
A | G | 8 | a0001c0001t0001g0256a0001c0001t0004g0170a0001c0001t0006g0169others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+10833A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969119 | ||||||
| chr6:104969159
|
C | T | 1 | a0001c0001t0004g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.198+10873C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969159 | ||||||
| chr6:104969377
|
A | T | 3 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0052 | 3 | HG01891.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.198+11091A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969377 | ||||||
| chr6:104969458
|
A | G | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+11172A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969458 | ||||||
| chr6:104969460
|
A | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.198+11174A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969460 | ||||||
| chr6:104969592
|
A | G | 1 | a0001c0001t0003g0096 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.198+11306A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969592 | ||||||
| chr6:104969611
|
A | ATATACTT others(19): Show |
1 | a0001c0001t0003g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.198+11326_198+1135 others(30): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104969611 | |||||
| chr6:104969875
|
T | C | 1 | a0001c0001t0007g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198+11589T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969875 | ||||||
| chr6:104969880
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.198+11594C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969880 | ||||||
| chr6:104969892
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.198+11606C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104969892 | ||||||
| chr6:104970103
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.198+11817G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104970103 | ||||||
| chr6:104970110
|
C | T | 1 | a0001c0001t0003g0267 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.198+11824C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104970110 | ||||||
| chr6:104970482
|
G | C | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+12196G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104970482 | ||||||
| chr6:104970837
|
A | C | 1 | a0001c0001t0003g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.198+12551A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104970837 | ||||||
| chr6:104970906
|
A | C | 1 | a0001c0001t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198+12620A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104970906 | ||||||
| chr6:104970918
|
T | A | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.198+12632T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104970918 | ||||||
| chr6:104970945
|
T | A | 3 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0002t0007g0005 | 3 | HG02145.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198+12659T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104970945 | ||||||
| chr6:104971296
|
TTTTA | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0164 | 3 | NA18946.hp2 NA18990.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.198+13014_198+1301 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104971296 | |||||
| chr6:104971411
|
T | A | 22 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.198+13125T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104971411 | ||||||
| chr6:104971591
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.198+13305G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104971591 | ||||||
| chr6:104971749
|
A | C | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+13463A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104971749 | ||||||
| chr6:104971960
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.198+13674A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104971960 | ||||||
| chr6:104971966
|
G | GTTATTTA others(1): Show |
7 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0071others(4): Show | 7 | HG01106.hp2 HG01167.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+13695_198+1370 others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104971966 | |||||
| chr6:104972115
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0111others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.198+13829T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104972115 | ||||||
| chr6:104972160
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.198+13874C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104972160 | ||||||
| chr6:104972161
|
G | A | 3 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058 | 3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.198+13875G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104972161 | ||||||
| chr6:104972702
|
G | T | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198+14416G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104972702 | ||||||
| chr6:104972975
|
G | T | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+14689G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104972975 | ||||||
| chr6:104973413
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.198+15127G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104973413 | ||||||
| chr6:104973442
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.198+15156C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104973442 | ||||||
| chr6:104973492
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198+15206C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104973492 | ||||||
| chr6:104973539
|
C | G | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+15253C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104973539 | ||||||
| chr6:104973540
|
A | G | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+15254A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104973540 | ||||||
| chr6:104973645
|
C | T | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+15359C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104973645 | ||||||
| chr6:104973839
|
C | A | 2 | a0001c0001t0003g0070a0001c0001t0003g0073 | 2 | NA18957.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.198+15553C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104973839 | ||||||
| chr6:104974065
|
A | G | 7 | a0001c0001t0002g0110a0001c0001t0003g0101a0001c0001t0003g0102others(4): Show | 7 | NA18947.hp2 NA18950.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+15779A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974065 | ||||||
| chr6:104974095
|
A | C | 2 | a0001c0001t0012g0233a0001c0001t0012g0234 | 2 | HG01255.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.198+15809A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974095 | ||||||
| chr6:104974317
|
C | T | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0025g0112 | 3 | HG02572.hp1 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.198+16031C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974317 | ||||||
| chr6:104974364
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+16078C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974364 | ||||||
| chr6:104974403
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.198+16117C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974403 | ||||||
| chr6:104974421
|
G | A | 1 | a0001c0001t0025g0112 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.198+16135G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974421 | ||||||
| chr6:104974467
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.198+16181C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974467 | ||||||
| chr6:104974488
|
C | CA | 9 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(6): Show | 9 | HG01433.hp2 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+16218dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104974488 | |||||
| chr6:104974809
|
A | AATT | 17 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(14): Show | 17 | HG00735.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+16545_198+1654 others(7): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104974809 | |||||
| chr6:104974938
|
G | T | 1 | a0001c0001t0015g0162 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.198+16652G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974938 | ||||||
| chr6:104974965
|
A | C | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+16679A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104974965 | ||||||
| chr6:104975623
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0009g0227 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.198+17337G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104975623 | ||||||
| chr6:104975638
|
G | A | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+17352G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104975638 | ||||||
| chr6:104975809
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.198+17523C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104975809 | ||||||
| chr6:104975841
|
C | CT | 31 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(28): Show | 31 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.198+17571dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104975841 | |||||
| chr6:104975867
|
G | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0004g0053 | 3 | HG00642.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.198+17581G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104975867 | ||||||
| chr6:104975942
|
A | G | 1 | a0002c0003t0002g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+17656A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104975942 | ||||||
| chr6:104975952
|
G | C | 5 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+17666G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104975952 | ||||||
| chr6:104975954
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.198+17668T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104975954 | ||||||
| chr6:104975991
|
A | G | 2 | a0001c0001t0003g0094a0001c0001t0004g0095 | 2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.198+17705A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104975991 | ||||||
| chr6:104976056
|
G | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.198+17770G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104976056 | ||||||
| chr6:104976451
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.198+18165A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104976451 | ||||||
| chr6:104976896
|
A | G | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+18610A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104976896 | ||||||
| chr6:104976921
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.198+18635A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104976921 | ||||||
| chr6:104977026
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0111others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.198+18740C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104977026 | ||||||
| chr6:104977120
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+18834C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104977120 | ||||||
| chr6:104977355
|
A | T | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+19069A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104977355 | ||||||
| chr6:104977766
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.198+19480C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104977766 | ||||||
| chr6:104977856
|
G | A | 7 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0071others(4): Show | 7 | HG01106.hp2 HG01167.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+19570G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104977856 | ||||||
| chr6:104977860
|
C | G | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+19574C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104977860 | ||||||
| chr6:104978048
|
T | A | 1 | a0001c0001t0002g0239 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.198+19762T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104978048 | ||||||
| chr6:104978151
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.198+19865C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104978151 | ||||||
| chr6:104978284
|
T | C | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+19998T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104978284 | ||||||
| chr6:104978358
|
G | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0004g0053 | 3 | HG00642.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.198+20072G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104978358 | ||||||
| chr6:104978901
|
A | G | 1 | a0001c0001t0002g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.198+20615A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104978901 | ||||||
| chr6:104978949
|
A | T | 1 | a0001c0001t0001g0179 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.198+20663A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104978949 | ||||||
| chr6:104979069
|
A | G | 8 | a0001c0001t0001g0115a0001c0001t0001g0158a0001c0001t0001g0159others(5): Show | 8 | HG00140.hp2 HG01255.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+20783A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979069 | ||||||
| chr6:104979119
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0111others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.198+20833A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979119 | ||||||
| chr6:104979228
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+20942T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979228 | ||||||
| chr6:104979290
|
A | C | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0025g0112 | 3 | HG02572.hp1 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.198+21004A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979290 | ||||||
| chr6:104979312
|
T | G | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+21026T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979312 | ||||||
| chr6:104979364
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.198+21078C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979364 | ||||||
| chr6:104979365
|
G | A | 1 | a0001c0001t0002g0200 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.198+21079G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979365 | ||||||
| chr6:104979396
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.198+21110C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979396 | ||||||
| chr6:104979455
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.198+21169C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979455 | ||||||
| chr6:104979671
|
T | G | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0025g0112 | 3 | HG02572.hp1 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.198+21385T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979671 | ||||||
| chr6:104979820
|
A | G | 1 | a0001c0001t0008g0157 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.198+21534A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104979820 | ||||||
| chr6:104980013
|
A | C | 1 | a0001c0001t0005g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.198+21727A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104980013 | ||||||
| chr6:104980433
|
A | C | 1 | a0001c0001t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.198+22147A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104980433 | ||||||
| chr6:104980449
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+22163G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104980449 | ||||||
| chr6:104980584
|
G | T | 4 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(1): Show | 4 | HG02056.hp2 NA18960.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+22298G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104980584 | ||||||
| chr6:104981096
|
A | G | 1 | a0001c0001t0003g0093 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+22810A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104981096 | ||||||
| chr6:104981144
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.198+22858C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104981144 | ||||||
| chr6:104981172
|
A | C | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.198+22886A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104981172 | ||||||
| chr6:104981280
|
G | A | 4 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0037others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+22994G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104981280 | ||||||
| chr6:104981354
|
T | A | 2 | a0001c0001t0002g0047a0001c0001t0007g0048 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.198+23068T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104981354 | ||||||
| chr6:104981636
|
C | T | 8 | a0001c0001t0001g0091a0001c0001t0001g0275a0001c0001t0003g0092others(5): Show | 8 | HG01258.hp2 HG01516.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+23350C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104981636 | ||||||
| chr6:104982130
|
C | T | 3 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058 | 3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.198+23844C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104982130 | ||||||
| chr6:104982290
|
G | A | 3 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171 | 3 | HG02976.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.198+24004G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104982290 | ||||||
| chr6:104982313
|
C | CA | 74 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(71): Show | 74 | HG00423.hp2 HG00735.hp1 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.198+24041dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104982313 | |||||
| chr6:104982375
|
T | C | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+24089T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104982375 | ||||||
| chr6:104982443
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.198+24157A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104982443 | ||||||
| chr6:104982628
|
A | T | 22 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.198+24342A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104982628 | ||||||
| chr6:104982697
|
C | T | 1 | a0001c0001t0009g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.198+24411C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104982697 | ||||||
| chr6:104982795
|
T | TTTTA | 5 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+24525_198+2452 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104982795 | |||||
| chr6:104982999
|
G | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+24713G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104982999 | ||||||
| chr6:104983059
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.198+24773C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983059 | ||||||
| chr6:104983309
|
G | A | 13 | a0001c0001t0002g0242a0001c0001t0002g0249a0001c0001t0002g0250others(10): Show | 14 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.198+25023G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983309 | ||||||
| chr6:104983323
|
A | C | 1 | a0001c0001t0014g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.198+25037A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983323 | ||||||
| chr6:104983351
|
G | A | 2 | a0001c0001t0002g0047a0001c0001t0007g0048 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.198+25065G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983351 | ||||||
| chr6:104983434
|
G | C | 1 | a0001c0001t0007g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198+25148G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983434 | ||||||
| chr6:104983645
|
C | T | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.198+25359C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983645 | ||||||
| chr6:104983654
|
G | A | 1 | a0001c0001t0002g0259 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.198+25368G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983654 | ||||||
| chr6:104983876
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.198+25590G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983876 | ||||||
| chr6:104983994
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198+25708C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104983994 | ||||||
| chr6:104984265
|
GTGTGTA | G | 3 | a0001c0001t0001g0002a0001c0001t0020g0120a0001c0001t0024g0156 | 3 | HG01169.hp2 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.198+25985_198+2599 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104984265 | |||||
| chr6:104984312
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+26026T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104984312 | ||||||
| chr6:104984768
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.198+26482A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104984768 | ||||||
| chr6:104984841
|
A | G | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+26555A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104984841 | ||||||
| chr6:104985015
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.198+26729C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104985015 | ||||||
| chr6:104985114
|
CTG | C | 13 | a0001c0001t0002g0242a0001c0001t0002g0249a0001c0001t0002g0250others(10): Show | 14 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.198+26830_198+2683 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104985114 | |||||
| chr6:104985119
|
G | C | 32 | a0001c0001t0001g0111a0001c0001t0001g0238a0001c0001t0001g0241others(29): Show | 33 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+26833G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104985119 | ||||||
| chr6:104985372
|
A | C | 3 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0004g0251 | 3 | HG00323.hp2 HG01074.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.198+27086A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104985372 | ||||||
| chr6:104985524
|
T | C | 1 | a0001c0001t0002g0242 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.198+27238T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104985524 | ||||||
| chr6:104985690
|
T | C | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+27404T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104985690 | ||||||
| chr6:104986203
|
T | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.198+27917T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104986203 | ||||||
| chr6:104986243
|
G | A | 3 | a0001c0001t0003g0067a0001c0001t0003g0071a0001c0001t0003g0107 | 3 | HG01978.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.198+27957G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104986243 | ||||||
| chr6:104986369
|
TTATC | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.198+28088_198+2809 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104986369 | |||||
| chr6:104986448
|
C | T | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+28162C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104986448 | ||||||
| chr6:104986484
|
T | G | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+28198T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104986484 | ||||||
| chr6:104986532
|
C | CA | 62 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(59): Show | 62 | HG00423.hp2 HG00735.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.198+28263dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104986532 | |||||
| chr6:104986532
|
C | CAA | 6 | a0001c0001t0001g0232a0001c0001t0002g0021a0001c0001t0002g0228others(3): Show | 6 | HG02615.hp1 NA18949.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+28262_198+2826 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104986532 | |||||
| chr6:104986532
|
CA | C | 12 | a0001c0001t0001g0015a0001c0001t0001g0123a0001c0001t0001g0158others(9): Show | 12 | HG01515.hp1 HG01517.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+28263delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104986532 | |||||
| chr6:104986532
|
CAA | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.198+28262_198+2826 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104986532 | |||||
| chr6:104986652
|
G | A | 1 | a0001c0001t0004g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.198+28366G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104986652 | ||||||
| chr6:104986786
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.198+28500A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104986786 | ||||||
| chr6:104987032
|
A | G | 22 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.198+28746A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104987032 | ||||||
| chr6:104987447
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.198+29161G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104987447 | ||||||
| chr6:104987495
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0004g0028others(3): Show | 6 | HG01891.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+29209C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104987495 | ||||||
| chr6:104987570
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198+29284C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104987570 | ||||||
| chr6:104987622
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.198+29336A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104987622 | ||||||
| chr6:104987811
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+29525C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104987811 | ||||||
| chr6:104988014
|
G | C | 1 | a0001c0001t0001g0232 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.198+29728G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104988014 | ||||||
| chr6:104988178
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0111others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.198+29892C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104988178 | ||||||
| chr6:104988273
|
A | G | 1 | a0001c0001t0007g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198+29987A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104988273 | ||||||
| chr6:104988569
|
A | AT | 130 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.198+30302dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104988569 | |||||
| chr6:104988569
|
AT | A | 5 | a0001c0001t0001g0039a0001c0001t0003g0070a0001c0001t0003g0099others(2): Show | 5 | HG01167.hp2 HG01516.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+30302delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104988569 | |||||
| chr6:104988669
|
T | C | 1 | a0001c0001t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198+30383T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104988669 | ||||||
| chr6:104988678
|
T | C | 3 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0052 | 3 | HG01891.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.198+30392T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104988678 | ||||||
| chr6:104989097
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.198+30811G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989097 | ||||||
| chr6:104989118
|
G | A | 22 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.198+30832G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989118 | ||||||
| chr6:104989163
|
T | A | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+30877T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989163 | ||||||
| chr6:104989251
|
A | C | 1 | a0001c0001t0011g0089 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.198+30965A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989251 | ||||||
| chr6:104989465
|
C | T | 1 | a0001c0001t0003g0088 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.198+31179C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989465 | ||||||
| chr6:104989576
|
G | GT | 98 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(95): Show | 98 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.198+31315dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104989576 | |||||
| chr6:104989576
|
G | GTT | 71 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0042others(68): Show | 71 | HG00140.hp1 HG00423.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.198+31314_198+3131 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104989576 | |||||
| chr6:104989576
|
G | GTTT | 24 | a0001c0001t0001g0123a0001c0001t0001g0155a0001c0001t0001g0216others(21): Show | 24 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.198+31313_198+3131 others(7): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104989576 | |||||
| chr6:104989576
|
G | GTTTT | 10 | a0001c0001t0001g0207a0001c0001t0002g0200a0001c0001t0002g0206others(7): Show | 10 | HG00423.hp1 HG00558.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+31312_198+3131 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104989576 | |||||
| chr6:104989576
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0126 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.198+31305_198+3131 others(15): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104989576 | |||||
| chr6:104989585
|
T | TTG | 26 | a0001c0001t0001g0111a0001c0001t0001g0238a0001c0001t0001g0241others(23): Show | 27 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.198+31300_198+3130 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104989585 | |||||
| chr6:104989590
|
T | G | 27 | a0001c0001t0001g0111a0001c0001t0001g0238a0001c0001t0001g0241others(24): Show | 28 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.198+31304T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989590 | ||||||
| chr6:104989595
|
T | G | 27 | a0001c0001t0001g0111a0001c0001t0001g0238a0001c0001t0001g0241others(24): Show | 28 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.198+31309T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989595 | ||||||
| chr6:104989632
|
C | T | 5 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+31346C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989632 | ||||||
| chr6:104989685
|
G | A | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198+31399G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989685 | ||||||
| chr6:104989695
|
G | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.198+31409G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989695 | ||||||
| chr6:104989705
|
TGCCTCA | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.198+31424_198+3142 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104989705 | |||||
| chr6:104989928
|
C | T | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+31642C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989928 | ||||||
| chr6:104989971
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+31685G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104989971 | ||||||
| chr6:104990112
|
T | G | 1 | a0001c0001t0010g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.198+31826T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990112 | ||||||
| chr6:104990203
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.198+31917T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990203 | ||||||
| chr6:104990340
|
A | G | 3 | a0001c0001t0003g0086a0001c0001t0011g0081a0001c0001t0011g0089 | 3 | HG02027.hp1 HG02074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.198+32054A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990340 | ||||||
| chr6:104990566
|
T | A | 1 | a0001c0001t0025g0112 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.198+32280T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990566 | ||||||
| chr6:104990569
|
AT | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.198+32296delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104990569 | |||||
| chr6:104990573
|
T | A | 3 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0260 | 3 | NA18942.hp1 NA18942.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.198+32287T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990573 | ||||||
| chr6:104990575
|
T | A | 11 | a0001c0001t0001g0026a0001c0001t0004g0003a0001c0001t0004g0004others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.198+32289T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990575 | ||||||
| chr6:104990576
|
T | A | 1 | a0001c0001t0023g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.198+32290T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990576 | ||||||
| chr6:104990577
|
T | A | 2 | a0001c0001t0001g0167a0001c0001t0019g0202 | 2 | NA18963.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.198+32291T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990577 | ||||||
| chr6:104990582
|
T | A | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+32296T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990582 | ||||||
| chr6:104990769
|
C | G | 8 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(5): Show | 8 | HG00423.hp1 HG00558.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+32483C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990769 | ||||||
| chr6:104990873
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.198+32587T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990873 | ||||||
| chr6:104990950
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+32664A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104990950 | ||||||
| chr6:104991089
|
C | CG | 24 | a0001c0001t0001g0026a0001c0001t0001g0126a0001c0001t0001g0130others(21): Show | 24 | HG01069.hp1 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.198+32807dupG | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104991089 | |||||
| chr6:104991089
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.198+32803C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991089 | ||||||
| chr6:104991134
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198+32848G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991134 | ||||||
| chr6:104991148
|
GC | G | 276 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.198+32869delC | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104991148 | |||||
| chr6:104991183
|
G | A | 1 | a0002c0003t0002g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+32897G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991183 | ||||||
| chr6:104991395
|
C | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0165 | 2 | HG02135.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.198+33109C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991395 | ||||||
| chr6:104991461
|
T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.198+33175T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991461 | ||||||
| chr6:104991479
|
A | G | 18 | a0001c0001t0001g0241a0001c0001t0002g0239a0001c0001t0002g0242others(15): Show | 19 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+33193A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991479 | ||||||
| chr6:104991483
|
C | T | 24 | a0001c0001t0001g0207a0001c0001t0001g0216a0001c0001t0002g0124others(21): Show | 24 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.198+33197C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991483 | ||||||
| chr6:104991539
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.198+33253G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991539 | ||||||
| chr6:104991609
|
G | C | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.198+33323G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991609 | ||||||
| chr6:104991617
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.198+33331C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991617 | ||||||
| chr6:104991748
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.198+33462C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991748 | ||||||
| chr6:104991797
|
G | A | 5 | a0001c0001t0003g0119a0001c0001t0007g0057a0001c0001t0013g0056others(2): Show | 5 | HG02055.hp1 HG02738.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+33511G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991797 | ||||||
| chr6:104991868
|
C | CG | 10 | a0001c0001t0001g0131a0001c0001t0001g0276a0001c0001t0002g0020others(7): Show | 10 | HG01106.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+33586dupG | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104991868 | |||||
| chr6:104991965
|
G | A | 78 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.198+33679G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104991965 | ||||||
| chr6:104992043
|
T | C | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198+33757T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992043 | ||||||
| chr6:104992070
|
G | GT | 8 | a0001c0001t0001g0141a0001c0001t0001g0197a0001c0001t0002g0031others(5): Show | 8 | HG00735.hp2 HG01106.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+33796dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992070 | |||||
| chr6:104992073
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0020g0120a0001c0001t0024g0156 | 3 | HG01169.hp2 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.198+33787T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992073 | ||||||
| chr6:104992187
|
A | G | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+33901A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992187 | ||||||
| chr6:104992211
|
TC | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0004g0053 | 3 | HG00642.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.198+33926delC | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992211 | ||||||
| chr6:104992298
|
C | G | 1 | a0001c0001t0005g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.199-34000C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992298 | ||||||
| chr6:104992299
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-33999C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992299 | ||||||
| chr6:104992303
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-33995C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992303 | ||||||
| chr6:104992365
|
A | G | 1 | a0002c0003t0002g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-33933A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992365 | ||||||
| chr6:104992449
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.199-33849T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992449 | ||||||
| chr6:104992484
|
T | TTG | 34 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0055others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.199-33784_199-3378 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992484 | |||||
| chr6:104992484
|
T | TTGTG | 26 | a0001c0001t0001g0051a0001c0001t0001g0177a0001c0001t0001g0232others(23): Show | 26 | HG01358.hp1 HG02257.hp1 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.199-33786_199-3378 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992484 | |||||
| chr6:104992484
|
TTG | T | 8 | a0001c0001t0001g0111a0001c0001t0001g0193a0001c0001t0002g0022others(5): Show | 8 | HG02074.hp1 HG02572.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-33784_199-3378 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992484 | |||||
| chr6:104992512
|
GTGTT | G | 5 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-33784_199-3378 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992512 | |||||
| chr6:104992514
|
G | GTGTGTT | 8 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(5): Show | 8 | HG01167.hp2 HG01255.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-33783_199-3378 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992514 | |||||
| chr6:104992514
|
G | GTGTT | 49 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(46): Show | 49 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.199-33783_199-3378 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992514 | |||||
| chr6:104992514
|
G | GTT | 22 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-33775_199-3377 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992514 | |||||
| chr6:104992514
|
G | T | 1 | a0001c0001t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.199-33784G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992514 | ||||||
| chr6:104992514
|
GTT | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0115others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.199-33775_199-3377 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104992514 | |||||
| chr6:104992516
|
T | G | 31 | a0001c0001t0001g0055a0001c0001t0001g0146a0001c0001t0001g0167others(28): Show | 31 | HG00099.hp2 HG01993.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.199-33782T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992516 | ||||||
| chr6:104992518
|
T | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0276a0001c0001t0003g0184others(1): Show | 4 | HG01258.hp1 HG02055.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-33780T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992518 | ||||||
| chr6:104992644
|
C | T | 1 | a0001c0001t0003g0270 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.199-33654C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992644 | ||||||
| chr6:104992741
|
C | A | 55 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(52): Show | 55 | HG00140.hp2 HG00558.hp1 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.199-33557C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992741 | ||||||
| chr6:104992867
|
T | G | 16 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(13): Show | 16 | HG00735.hp1 HG01243.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-33431T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104992867 | ||||||
| chr6:104993239
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-33059G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104993239 | ||||||
| chr6:104993327
|
G | A | 5 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-32971G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104993327 | ||||||
| chr6:104993386
|
T | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-32912T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104993386 | ||||||
| chr6:104993529
|
T | G | 22 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-32769T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104993529 | ||||||
| chr6:104993625
|
C | T | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-32673C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104993625 | ||||||
| chr6:104993767
|
G | A | 4 | a0001c0001t0001g0238a0001c0001t0002g0236a0001c0001t0014g0235others(1): Show | 4 | HG01515.hp2 HG02622.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-32531G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104993767 | ||||||
| chr6:104993775
|
C | T | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-32523C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104993775 | ||||||
| chr6:104993833
|
C | CA | 71 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(68): Show | 71 | HG00423.hp2 HG00735.hp1 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.199-32447dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104993833 | |||||
| chr6:104993833
|
CA | C | 8 | a0001c0001t0002g0209a0001c0001t0004g0170a0001c0001t0006g0169others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-32447delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104993833 | |||||
| chr6:104993996
|
T | C | 1 | a0001c0001t0002g0166 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.199-32302T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104993996 | ||||||
| chr6:104994004
|
A | AAT | 3 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0002t0007g0005 | 3 | HG02145.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.199-32281_199-3228 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104994004 | |||||
| chr6:104994006
|
T | A | 1 | a0001c0001t0007g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.199-32292T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994006 | ||||||
| chr6:104994013
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.199-32285A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994013 | ||||||
| chr6:104994090
|
C | T | 1 | a0001c0001t0010g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.199-32208C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994090 | ||||||
| chr6:104994114
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG00323.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.199-32184C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994114 | ||||||
| chr6:104994441
|
C | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0111others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.199-31857C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994441 | ||||||
| chr6:104994452
|
T | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0111others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.199-31846T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994452 | ||||||
| chr6:104994561
|
T | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-31737T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994561 | ||||||
| chr6:104994762
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.199-31536C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994762 | ||||||
| chr6:104994937
|
T | C | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.199-31361T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994937 | ||||||
| chr6:104994940
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.199-31358C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994940 | ||||||
| chr6:104994983
|
A | G | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-31315A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104994983 | ||||||
| chr6:104995188
|
G | T | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.199-31110G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995188 | ||||||
| chr6:104995314
|
T | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.199-30984T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995314 | ||||||
| chr6:104995383
|
G | C | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.199-30915G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995383 | ||||||
| chr6:104995431
|
G | C | 1 | a0001c0001t0002g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-30867G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995431 | ||||||
| chr6:104995436
|
C | G | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-30862C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995436 | ||||||
| chr6:104995479
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.199-30819G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995479 | ||||||
| chr6:104995653
|
C | T | 1 | a0001c0001t0003g0080 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.199-30645C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995653 | ||||||
| chr6:104995696
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.199-30602C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995696 | ||||||
| chr6:104995925
|
G | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-30373G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104995925 | ||||||
| chr6:104995965
|
T | TTA | 10 | a0001c0001t0001g0118a0001c0001t0001g0125a0001c0001t0001g0137others(7): Show | 10 | HG00558.hp1 HG02027.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-30318_199-3031 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104995965 | |||||
| chr6:104995965
|
TTA | T | 5 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(2): Show | 5 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-30318_199-3031 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104995965 | |||||
| chr6:104996183
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.199-30115C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104996183 | ||||||
| chr6:104996240
|
T | C | 22 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-30058T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104996240 | ||||||
| chr6:104996352
|
C | G | 1 | a0002c0003t0002g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-29946C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104996352 | ||||||
| chr6:104996542
|
C | G | 2 | a0001c0001t0003g0189a0001c0001t0018g0190 | 2 | NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.199-29756C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104996542 | ||||||
| chr6:104996578
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.199-29720A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104996578 | ||||||
| chr6:104996657
|
C | T | 3 | a0001c0001t0003g0148a0001c0001t0008g0132a0001c0001t0008g0147 | 3 | NA18948.hp2 NA19009.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.199-29641C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104996657 | ||||||
| chr6:104996700
|
A | G | 3 | a0001c0001t0003g0069a0001c0001t0003g0094a0001c0001t0004g0095 | 3 | HG02109.hp2 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.199-29598A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104996700 | ||||||
| chr6:104996820
|
T | TA | 3 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0002t0007g0005 | 3 | HG02145.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.199-29473dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104996820 | |||||
| chr6:104996859
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.199-29439C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104996859 | ||||||
| chr6:104996914
|
GT | G | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(1): Show | 4 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-29381delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104996914 | |||||
| chr6:104997098
|
G | A | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-29200G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997098 | ||||||
| chr6:104997174
|
G | A | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-29124G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997174 | ||||||
| chr6:104997269
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.199-29029A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997269 | ||||||
| chr6:104997285
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0003g0070 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.199-29008_199-2899 others(15): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104997285 | |||||
| chr6:104997301
|
GAAAAA | G | 21 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(18): Show | 22 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.199-28996_199-2899 others(9): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997301 | ||||||
| chr6:104997306
|
A | G | 1 | a0001c0001t0004g0240 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.199-28992A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997306 | ||||||
| chr6:104997489
|
A | G | 71 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(68): Show | 71 | HG00423.hp2 HG00735.hp1 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.199-28809A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997489 | ||||||
| chr6:104997654
|
G | A | 5 | a0001c0001t0002g0110a0001c0001t0003g0103a0001c0001t0003g0104others(2): Show | 5 | NA18947.hp2 NA18984.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-28644G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997654 | ||||||
| chr6:104997655
|
G | T | 5 | a0001c0001t0002g0110a0001c0001t0003g0103a0001c0001t0003g0104others(2): Show | 5 | NA18947.hp2 NA18984.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-28643G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997655 | ||||||
| chr6:104997944
|
T | C | 1 | a0001c0001t0003g0065 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.199-28354T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104997944 | ||||||
| chr6:104998252
|
T | G | 1 | a0001c0001t0003g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.199-28046T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104998252 | ||||||
| chr6:104998417
|
GTTTAA | G | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-27877_199-2787 others(9): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 104998417 | |||||
| chr6:104998933
|
A | G | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-27365A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104998933 | ||||||
| chr6:104998999
|
A | G | 1 | a0001c0001t0004g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199-27299A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104998999 | ||||||
| chr6:104999020
|
G | T | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-27278G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999020 | ||||||
| chr6:104999021
|
A | C | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-27277A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999021 | ||||||
| chr6:104999112
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.199-27186G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999112 | ||||||
| chr6:104999169
|
A | T | 1 | a0001c0001t0007g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.199-27129A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999169 | ||||||
| chr6:104999320
|
G | A | 85 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(82): Show | 85 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.199-26978G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999320 | ||||||
| chr6:104999423
|
C | G | 1 | a0001c0001t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.199-26875C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999423 | ||||||
| chr6:104999512
|
A | C | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-26786A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999512 | ||||||
| chr6:104999634
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-26664A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999634 | ||||||
| chr6:104999868
|
C | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0004g0053 | 3 | HG00642.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.199-26430C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999868 | ||||||
| chr6:104999925
|
G | C | 2 | a0001c0001t0002g0122a0001c0001t0009g0227 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.199-26373G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 104999925 | ||||||
| chr6:105000146
|
C | T | 11 | a0001c0001t0001g0051a0001c0001t0005g0019a0001c0001t0005g0034others(8): Show | 11 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-26152C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105000146 | ||||||
| chr6:105000165
|
ATG | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.199-26131_199-2613 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105000165 | |||||
| chr6:105000411
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.199-25887C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105000411 | ||||||
| chr6:105000609
|
G | C | 14 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(11): Show | 14 | HG00735.hp1 HG01243.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-25689G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105000609 | ||||||
| chr6:105000749
|
G | A | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-25549G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105000749 | ||||||
| chr6:105000984
|
T | C | 1 | a0001c0001t0002g0228 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.199-25314T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105000984 | ||||||
| chr6:105000991
|
ATT | A | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-25306_199-2530 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105000991 | ||||||
| chr6:105001205
|
A | G | 2 | a0001c0001t0002g0047a0001c0001t0007g0048 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.199-25093A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105001205 | ||||||
| chr6:105001402
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.199-24896T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105001402 | ||||||
| chr6:105001696
|
G | A | 3 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0002t0007g0005 | 3 | HG02145.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.199-24602G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105001696 | ||||||
| chr6:105001834
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.199-24464G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105001834 | ||||||
| chr6:105001927
|
C | A | 1 | a0001c0001t0001g0178 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.199-24371C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105001927 | ||||||
| chr6:105002166
|
A | AT | 16 | a0001c0001t0001g0015a0001c0001t0001g0151a0001c0001t0001g0192others(13): Show | 16 | HG01106.hp2 HG01243.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-24109dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105002166 | |||||
| chr6:105002166
|
AT | A | 7 | a0001c0001t0001g0055a0001c0001t0001g0225a0001c0001t0002g0122others(4): Show | 7 | HG00323.hp2 HG01981.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-24109delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105002166 | |||||
| chr6:105002166
|
ATT | A | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-24110_199-2410 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105002166 | |||||
| chr6:105002355
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.199-23943A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105002355 | ||||||
| chr6:105002454
|
G | A | 1 | a0001c0001t0003g0065 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.199-23844G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105002454 | ||||||
| chr6:105002532
|
T | C | 1 | a0001c0001t0011g0076 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.199-23766T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105002532 | ||||||
| chr6:105002565
|
C | T | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-23733C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105002565 | ||||||
| chr6:105002599
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.199-23699G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105002599 | ||||||
| chr6:105003010
|
C | A | 1 | a0001c0001t0007g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.199-23288C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105003010 | ||||||
| chr6:105003124
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-23174C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105003124 | ||||||
| chr6:105003910
|
C | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0004g0053 | 3 | HG00642.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.199-22388C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105003910 | ||||||
| chr6:105003935
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.199-22363T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105003935 | ||||||
| chr6:105003967
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.199-22331A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105003967 | ||||||
| chr6:105004010
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-22288G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004010 | ||||||
| chr6:105004031
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.199-22267T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004031 | ||||||
| chr6:105004150
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.199-22148T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004150 | ||||||
| chr6:105004154
|
A | G | 86 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0041others(83): Show | 86 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.199-22144A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004154 | ||||||
| chr6:105004281
|
C | T | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-22017C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004281 | ||||||
| chr6:105004344
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0003g0149 | 2 | NA18940.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.199-21954G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004344 | ||||||
| chr6:105004420
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0042 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-21878A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004420 | ||||||
| chr6:105004435
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.199-21863C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004435 | ||||||
| chr6:105004852
|
C | T | 1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.199-21446C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105004852 | ||||||
| chr6:105005003
|
G | C | 1 | a0001c0001t0026g0261 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.199-21295G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105005003 | ||||||
| chr6:105005209
|
T | C | 2 | a0001c0001t0004g0113a0001c0001t0004g0114 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.199-21089T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105005209 | ||||||
| chr6:105005446
|
G | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-20852G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105005446 | ||||||
| chr6:105005478
|
G | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-20820G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105005478 | ||||||
| chr6:105005542
|
A | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.199-20756A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105005542 | ||||||
| chr6:105005586
|
T | G | 1 | a0001c0001t0025g0112 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.199-20712T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105005586 | ||||||
| chr6:105005965
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.199-20333A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105005965 | ||||||
| chr6:105005992
|
T | C | 10 | a0001c0001t0001g0111a0001c0001t0002g0020a0001c0001t0002g0023others(7): Show | 10 | HG01433.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-20306T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105005992 | ||||||
| chr6:105006000
|
G | A | 1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.199-20298G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006000 | ||||||
| chr6:105006170
|
A | G | 1 | a0001c0001t0019g0202 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.199-20128A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006170 | ||||||
| chr6:105006176
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.199-20122A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006176 | ||||||
| chr6:105006214
|
T | C | 1 | a0001c0001t0002g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.199-20084T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006214 | ||||||
| chr6:105006303
|
C | CTGTTT | 9 | a0001c0001t0001g0181a0001c0001t0001g0188a0001c0001t0001g0195others(6): Show | 9 | HG01258.hp1 HG01943.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-19972_199-1996 others(9): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105006303 | |||||
| chr6:105006342
|
C | T | 3 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058 | 3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.199-19956C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006342 | ||||||
| chr6:105006460
|
C | T | 1 | a0001c0001t0006g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.199-19838C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006460 | ||||||
| chr6:105006503
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199-19795G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006503 | ||||||
| chr6:105006585
|
T | A | 1 | a0001c0001t0002g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-19713T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006585 | ||||||
| chr6:105006924
|
T | A | 23 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(20): Show | 24 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-19374T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006924 | ||||||
| chr6:105006943
|
G | A | 1 | a0001c0001t0004g0001 | 2 | NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.199-19355G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006943 | ||||||
| chr6:105006952
|
G | A | 3 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0052 | 3 | HG01891.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.199-19346G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105006952 | ||||||
| chr6:105007175
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.199-19123T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105007175 | ||||||
| chr6:105007368
|
G | T | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-18930G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105007368 | ||||||
| chr6:105007509
|
A | G | 1 | a0001c0001t0006g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.199-18789A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105007509 | ||||||
| chr6:105007531
|
CT | C | 8 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0133others(5): Show | 8 | HG00558.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-18754delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105007531 | |||||
| chr6:105007533
|
T | C | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-18765T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105007533 | ||||||
| chr6:105007585
|
T | G | 1 | a0001c0001t0004g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-18713T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105007585 | ||||||
| chr6:105007836
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.199-18462G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105007836 | ||||||
| chr6:105008161
|
AGGTTATT others(6): Show |
A | 1 | a0001c0001t0001g0222 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.199-18136_199-1812 others(17): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008161 | ||||||
| chr6:105008263
|
A | C | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-18035A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008263 | ||||||
| chr6:105008338
|
T | A | 1 | a0001c0001t0016g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199-17960T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008338 | ||||||
| chr6:105008359
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.199-17939G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008359 | ||||||
| chr6:105008378
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.199-17920C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008378 | ||||||
| chr6:105008382
|
C | T | 1 | a0001c0001t0004g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-17916C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008382 | ||||||
| chr6:105008383
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0191 | 2 | NA18957.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.199-17915G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008383 | ||||||
| chr6:105008394
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG00735.hp1 HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.199-17904C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008394 | ||||||
| chr6:105008472
|
G | A | 1 | a0001c0001t0027g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.199-17826G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008472 | ||||||
| chr6:105008505
|
G | A | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-17793G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008505 | ||||||
| chr6:105008568
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.199-17730C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008568 | ||||||
| chr6:105008600
|
T | C | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-17698T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008600 | ||||||
| chr6:105008744
|
C | T | 4 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-17554C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008744 | ||||||
| chr6:105008843
|
G | T | 1 | a0001c0001t0002g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.199-17455G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105008843 | ||||||
| chr6:105009065
|
T | G | 1 | a0001c0001t0013g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.199-17233T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105009065 | ||||||
| chr6:105009088
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0002g0228a0001c0001t0002g0229others(2): Show | 5 | NA18949.hp1 NA18952.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-17210C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105009088 | ||||||
| chr6:105009311
|
T | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.199-16987T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105009311 | ||||||
| chr6:105009584
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199-16714G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105009584 | ||||||
| chr6:105009666
|
C | A | 3 | a0001c0001t0003g0086a0001c0001t0011g0081a0001c0001t0011g0089 | 3 | HG02027.hp1 HG02074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.199-16632C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105009666 | ||||||
| chr6:105010131
|
A | G | 6 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0212others(3): Show | 6 | HG00423.hp1 HG00558.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-16167A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105010131 | ||||||
| chr6:105010192
|
C | CA | 6 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0002g0023others(3): Show | 6 | HG00323.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-16095dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105010192 | |||||
| chr6:105010355
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.199-15943C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105010355 | ||||||
| chr6:105010362
|
C | CA | 10 | a0001c0001t0001g0111a0001c0001t0001g0141a0001c0001t0002g0273others(7): Show | 10 | HG02135.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-15920dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105010362 | |||||
| chr6:105010497
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.199-15801T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105010497 | ||||||
| chr6:105010577
|
A | G | 1 | a0001c0001t0016g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.199-15721A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105010577 | ||||||
| chr6:105011182
|
A | G | 1 | a0001c0001t0005g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.199-15116A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011182 | ||||||
| chr6:105011261
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-15037C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011261 | ||||||
| chr6:105011272
|
C | T | 1 | a0001c0001t0019g0202 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.199-15026C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011272 | ||||||
| chr6:105011418
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0004g0054 | 2 | HG01358.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.199-14880G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011418 | ||||||
| chr6:105011483
|
C | G | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-14815C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011483 | ||||||
| chr6:105011569
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.199-14729T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011569 | ||||||
| chr6:105011679
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.199-14619G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011679 | ||||||
| chr6:105011890
|
T | G | 5 | a0001c0001t0001g0238a0001c0001t0002g0236a0001c0001t0006g0154others(2): Show | 5 | HG01515.hp2 HG02622.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-14408T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011890 | ||||||
| chr6:105011950
|
G | A | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-14348G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105011950 | ||||||
| chr6:105012097
|
G | T | 1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.199-14201G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105012097 | ||||||
| chr6:105012191
|
G | T | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-14107G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105012191 | ||||||
| chr6:105012237
|
G | A | 1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.199-14061G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105012237 | ||||||
| chr6:105012245
|
A | G | 2 | a0001c0001t0002g0047a0001c0001t0007g0048 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.199-14053A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105012245 | ||||||
| chr6:105012335
|
G | T | 1 | a0001c0001t0003g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.199-13963G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105012335 | ||||||
| chr6:105012415
|
G | C | 1 | a0001c0001t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199-13883G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105012415 | ||||||
| chr6:105012581
|
T | C | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-13717T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105012581 | ||||||
| chr6:105012880
|
A | T | 2 | a0001c0001t0003g0068a0001c0001t0003g0108 | 2 | HG01106.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.199-13418A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105012880 | ||||||
| chr6:105013253
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.199-13045C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105013253 | ||||||
| chr6:105013291
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02572.hp1 HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.199-13007G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105013291 | ||||||
| chr6:105013431
|
A | C | 1 | a0001c0001t0003g0265 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.199-12867A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105013431 | ||||||
| chr6:105013467
|
G | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-12831G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105013467 | ||||||
| chr6:105013499
|
A | G | 2 | a0001c0001t0003g0094a0001c0001t0004g0095 | 2 | HG02109.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.199-12799A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105013499 | ||||||
| chr6:105013569
|
C | A | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-12729C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105013569 | ||||||
| chr6:105013723
|
CA | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.199-12559delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105013723 | |||||
| chr6:105013739
|
A | T | 1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-12559A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105013739 | ||||||
| chr6:105013931
|
A | G | 1 | a0001c0001t0007g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.199-12367A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105013931 | ||||||
| chr6:105014007
|
T | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.199-12291T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014007 | ||||||
| chr6:105014010
|
G | A | 52 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0001g0232others(49): Show | 52 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.199-12288G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014010 | ||||||
| chr6:105014076
|
C | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-12222C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014076 | ||||||
| chr6:105014129
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.199-12169G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014129 | ||||||
| chr6:105014230
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.199-12068T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014230 | ||||||
| chr6:105014326
|
T | A | 23 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(20): Show | 24 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-11972T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014326 | ||||||
| chr6:105014413
|
G | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-11885G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014413 | ||||||
| chr6:105014615
|
C | A | 1 | a0001c0001t0002g0213 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.199-11683C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014615 | ||||||
| chr6:105014830
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0042 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-11468T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014830 | ||||||
| chr6:105014836
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-11462A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014836 | ||||||
| chr6:105014989
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.199-11309A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105014989 | ||||||
| chr6:105015001
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.199-11297T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105015001 | ||||||
| chr6:105015262
|
A | G | 3 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0052 | 3 | HG01891.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.199-11036A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105015262 | ||||||
| chr6:105015441
|
C | T | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-10857C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105015441 | ||||||
| chr6:105015577
|
G | A | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-10721G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105015577 | ||||||
| chr6:105016351
|
A | G | 2 | a0001c0001t0004g0113a0001c0001t0004g0114 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.199-9947A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105016351 | ||||||
| chr6:105016369
|
G | A | 9 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(6): Show | 9 | HG01515.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-9929G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105016369 | ||||||
| chr6:105016445
|
T | C | 1 | a0001c0001t0013g0056 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.199-9853T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105016445 | ||||||
| chr6:105016551
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.199-9747C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105016551 | ||||||
| chr6:105016714
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-9584A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105016714 | ||||||
| chr6:105017008
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-9290G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105017008 | ||||||
| chr6:105017050
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-9248G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105017050 | ||||||
| chr6:105017065
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.199-9233T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105017065 | ||||||
| chr6:105017072
|
C | CAAA | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0161others(3): Show | 6 | HG01255.hp2 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-9207_199-9205d others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105017072 | |||||
| chr6:105017072
|
CA | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.199-9205delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105017072 | |||||
| chr6:105017072
|
CAA | C | 14 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0168others(11): Show | 14 | HG01169.hp1 HG02572.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-9206_199-9205d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105017072 | |||||
| chr6:105017182
|
C | G | 2 | a0001c0001t0002g0199a0001c0001t0002g0217 | 2 | NA18962.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.199-9116C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105017182 | ||||||
| chr6:105017350
|
C | G | 1 | a0001c0001t0006g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.199-8948C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105017350 | ||||||
| chr6:105017796
|
C | G | 1 | a0001c0001t0011g0076 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.199-8502C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105017796 | ||||||
| chr6:105018101
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.199-8197C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105018101 | ||||||
| chr6:105018115
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.199-8183G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105018115 | ||||||
| chr6:105018336
|
A | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.199-7962A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105018336 | ||||||
| chr6:105018457
|
G | A | 123 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.199-7841G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105018457 | ||||||
| chr6:105018655
|
T | C | 1 | a0001c0001t0006g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.199-7643T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105018655 | ||||||
| chr6:105018826
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.199-7472C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105018826 | ||||||
| chr6:105018839
|
A | T | 1 | a0001c0001t0003g0149 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.199-7459A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105018839 | ||||||
| chr6:105019126
|
T | G | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.199-7172T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105019126 | ||||||
| chr6:105019390
|
G | A | 1 | a0001c0001t0007g0255 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.199-6908G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105019390 | ||||||
| chr6:105019393
|
T | C | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.199-6905T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105019393 | ||||||
| chr6:105019647
|
A | G | 1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.199-6651A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105019647 | ||||||
| chr6:105019846
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.199-6452A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105019846 | ||||||
| chr6:105020107
|
C | CT | 28 | a0001c0001t0001g0165a0001c0001t0001g0178a0001c0001t0001g0185others(25): Show | 28 | HG01515.hp2 HG02451.hp1 HG02572.hp2 others(25): Show |
intron_variant | MODIFIER | c.199-6167dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105020107 | |||||
| chr6:105020107
|
CT | C | 37 | a0001c0001t0001g0039a0001c0001t0001g0051a0001c0001t0001g0111others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.199-6167delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105020107 | |||||
| chr6:105020107
|
CTT | C | 18 | a0001c0001t0001g0256a0001c0001t0002g0239a0001c0001t0002g0242others(15): Show | 19 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.199-6168_199-6167d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105020107 | |||||
| chr6:105020344
|
A | AT | 36 | a0001c0001t0001g0125a0001c0001t0001g0139a0001c0001t0002g0110others(33): Show | 37 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.199-5942dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105020344 | |||||
| chr6:105020366
|
G | A | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.199-5932G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020366 | ||||||
| chr6:105020450
|
G | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-5848G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020450 | ||||||
| chr6:105020521
|
G | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0178a0001c0001t0008g0132others(2): Show | 5 | NA18948.hp2 NA19009.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-5777G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020521 | ||||||
| chr6:105020556
|
C | G | 1 | a0001c0001t0003g0203 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.199-5742C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020556 | ||||||
| chr6:105020747
|
C | CT | 9 | a0001c0001t0001g0155a0001c0001t0001g0193a0001c0001t0002g0160others(6): Show | 9 | HG02004.hp2 HG02074.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-5528dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105020747 | |||||
| chr6:105020747
|
CT | C | 142 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0026others(139): Show | 143 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.199-5528delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105020747 | |||||
| chr6:105020747
|
CTT | C | 8 | a0001c0001t0002g0022a0001c0001t0002g0064a0001c0001t0002g0242others(5): Show | 8 | HG01167.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-5529_199-5528d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105020747 | |||||
| chr6:105020840
|
C | T | 1 | a0001c0001t0004g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-5458C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020840 | ||||||
| chr6:105020898
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.199-5400G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020898 | ||||||
| chr6:105020945
|
T | A | 1 | a0001c0001t0003g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.199-5353T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020945 | ||||||
| chr6:105020946
|
G | T | 1 | a0001c0001t0003g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.199-5352G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020946 | ||||||
| chr6:105020958
|
T | G | 1 | a0001c0001t0004g0254 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.199-5340T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105020958 | ||||||
| chr6:105021004
|
C | T | 14 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(11): Show | 14 | HG00735.hp1 HG01243.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-5294C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021004 | ||||||
| chr6:105021010
|
C | T | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-5288C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021010 | ||||||
| chr6:105021076
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.199-5222C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021076 | ||||||
| chr6:105021120
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.199-5178T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021120 | ||||||
| chr6:105021237
|
G | GTA | 5 | a0001c0001t0001g0232a0001c0001t0002g0228a0001c0001t0002g0229others(2): Show | 5 | NA18949.hp1 NA18952.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-5052_199-5051d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105021237 | |||||
| chr6:105021268
|
C | T | 1 | a0001c0001t0003g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.199-5030C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021268 | ||||||
| chr6:105021492
|
A | G | 22 | a0001c0001t0002g0239a0001c0001t0002g0242a0001c0001t0002g0249others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-4806A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021492 | ||||||
| chr6:105021572
|
T | C | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.199-4726T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021572 | ||||||
| chr6:105021601
|
C | T | 22 | a0001c0001t0002g0239a0001c0001t0002g0242a0001c0001t0002g0249others(19): Show | 23 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-4697C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021601 | ||||||
| chr6:105021636
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.199-4662T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021636 | ||||||
| chr6:105021646
|
T | A | 2 | a0001c0001t0002g0122a0001c0001t0009g0227 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.199-4652T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021646 | ||||||
| chr6:105021914
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.199-4384G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105021914 | ||||||
| chr6:105022063
|
A | G | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-4235A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105022063 | ||||||
| chr6:105022149
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.199-4149G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105022149 | ||||||
| chr6:105022173
|
G | A | 1 | a0001c0001t0004g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.199-4125G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105022173 | ||||||
| chr6:105022184
|
G | GTAATCTA others(14): Show |
1 | a0001c0001t0003g0149 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.199-4110_199-4109i others(23): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105022184 | |||||
| chr6:105022459
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.199-3839G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105022459 | ||||||
| chr6:105022516
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.199-3782G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105022516 | ||||||
| chr6:105022738
|
A | C | 1 | a0001c0001t0003g0149 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.199-3560A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105022738 | ||||||
| chr6:105022949
|
A | T | 1 | a0001c0001t0003g0149 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.199-3349A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105022949 | ||||||
| chr6:105023074
|
A | AAATACAG others(6): Show |
1 | a0001c0001t0002g0210 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.199-3220_199-3208d others(15): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023074 | |||||
| chr6:105023113
|
T | C | 1 | a0001c0001t0002g0211 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.199-3185T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023113 | ||||||
| chr6:105023210
|
G | GAT | 117 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.199-3072_199-3071d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023210 | |||||
| chr6:105023210
|
G | GATAT | 4 | a0001c0001t0001g0181a0001c0001t0002g0166a0001c0001t0004g0003others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3074_199-3071d others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023210 | |||||
| chr6:105023210
|
GAT | G | 9 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(6): Show | 9 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-3072_199-3071d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023210 | |||||
| chr6:105023217
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0003g0264 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.199-3073_199-3072i others(34): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023217 | |||||
| chr6:105023224
|
T | TAATATAT others(26): Show |
1 | a0001c0001t0001g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.199-3073_199-3072i others(35): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023224 | |||||
| chr6:105023226
|
T | A | 2 | a0001c0001t0001g0258a0001c0001t0003g0264 | 2 | HG02135.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.199-3072T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023226 | ||||||
| chr6:105023226
|
T | TAATATAT others(27): Show |
10 | a0001c0001t0001g0257a0001c0001t0002g0259a0001c0001t0002g0260others(7): Show | 10 | NA18942.hp2 NA18948.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-3071_199-3038d others(36): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023226 | |||||
| chr6:105023228
|
A | T | 1 | a0001c0001t0003g0149 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.199-3070A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023228 | ||||||
| chr6:105023229
|
T | A | 1 | a0001c0001t0003g0149 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.199-3069T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023229 | ||||||
| chr6:105023261
|
T | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-3037T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023261 | ||||||
| chr6:105023283
|
T | A | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-3015T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023283 | ||||||
| chr6:105023284
|
A | T | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-3014A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023284 | ||||||
| chr6:105023285
|
A | T | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-3013A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023285 | ||||||
| chr6:105023289
|
A | T | 3 | a0001c0001t0001g0256a0001c0001t0011g0081a0001c0001t0017g0176 | 3 | HG02074.hp2 HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.199-3009A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023289 | ||||||
| chr6:105023289
|
ATATATAT others(3): Show |
A | 4 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(1): Show | 4 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3000_199-2991d others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023289 | |||||
| chr6:105023295
|
ATAT | A | 6 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0007g0057others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-3001_199-2999d others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023295 | |||||
| chr6:105023297
|
AT | A | 123 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.199-2998delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023297 | |||||
| chr6:105023298
|
T | A | 3 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171 | 3 | HG02976.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.199-3000T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023298 | ||||||
| chr6:105023299
|
T | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.199-2999T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023299 | ||||||
| chr6:105023299
|
T | TTATATAT others(17): Show |
2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.199-2809_199-2786d others(26): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023299 | |||||
| chr6:105023299
|
T | TTATATAT others(41): Show |
1 | a0001c0001t0001g0257 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.199-2833_199-2786d others(50): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023299 | |||||
| chr6:105023299
|
T | TTATATAT others(261): Show |
1 | a0001c0001t0009g0017 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.199-2947_199-2946i others(270): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023299 | |||||
| chr6:105023299
|
T | TTATATTA others(7): Show |
3 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171 | 3 | HG02976.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.199-2994_199-2993i others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023299 | |||||
| chr6:105023302
|
T | TATATAAT others(257): Show |
1 | a0001c0001t0001g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.199-2947_199-2946i others(266): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023302 | |||||
| chr6:105023313
|
A | C | 1 | a0001c0001t0003g0149 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.199-2985A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023313 | ||||||
| chr6:105023315
|
T | A | 1 | a0001c0001t0002g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-2983T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023315 | ||||||
| chr6:105023329
|
A | C | 1 | a0001c0001t0003g0090 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.199-2969A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023329 | ||||||
| chr6:105023340
|
A | T | 1 | a0001c0001t0003g0077 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.199-2958A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023340 | ||||||
| chr6:105023347
|
A | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0186a0001c0001t0002g0145 | 3 | HG06807.hp2 NA18964.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.199-2951A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023347 | ||||||
| chr6:105023350
|
T | TAATTATA others(165): Show |
1 | a0001c0001t0002g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.199-2947_199-2946i others(174): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023350 | |||||
| chr6:105023350
|
T | TATATAAT others(56): Show |
1 | a0001c0001t0005g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.199-2911_199-2910i others(65): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023350 | |||||
| chr6:105023357
|
T | A | 1 | a0001c0001t0025g0112 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.199-2941T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023357 | ||||||
| chr6:105023358
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.199-2940T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023358 | ||||||
| chr6:105023359
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.199-2939A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023359 | ||||||
| chr6:105023360
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.199-2938T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023360 | ||||||
| chr6:105023361
|
A | ATATAATA others(10): Show |
1 | a0001c0001t0002g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-2936_199-2935i others(19): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023361 | |||||
| chr6:105023362
|
T | TTATATAT others(2): Show |
4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2925_199-2917d others(11): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023362 | |||||
| chr6:105023363
|
T | A | 1 | a0001c0001t0004g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-2935T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023363 | ||||||
| chr6:105023364
|
A | T | 1 | a0001c0001t0004g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-2934A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023364 | ||||||
| chr6:105023371
|
A | T | 1 | a0001c0001t0001g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.199-2927A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023371 | ||||||
| chr6:105023372
|
T | A | 1 | a0001c0001t0001g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.199-2926T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023372 | ||||||
| chr6:105023372
|
T | TATATATA others(78): Show |
1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-2912_199-2911i others(87): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023372 | |||||
| chr6:105023372
|
T | TATATATA others(15): Show |
1 | a0001c0001t0003g0077 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.199-2918_199-2897d others(24): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023372 | |||||
| chr6:105023374
|
T | TATATAAT others(32): Show |
1 | a0001c0001t0002g0253 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.199-2912_199-2911i others(41): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023374 | |||||
| chr6:105023375
|
A | ATATAATT others(79): Show |
1 | a0002c0003t0002g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-2911_199-2910i others(88): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023375 | |||||
| chr6:105023381
|
T | A | 8 | a0001c0001t0002g0122a0001c0001t0002g0199a0001c0001t0002g0211others(5): Show | 8 | HG00558.hp2 HG02615.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-2917T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023381 | ||||||
| chr6:105023381
|
TTATATTA others(30): Show |
T | 1 | a0001c0001t0004g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-2916_199-2880d others(39): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023381 | ||||||
| chr6:105023386
|
T | TATAA | 3 | a0001c0001t0001g0241a0001c0001t0002g0236a0001c0001t0002g0252 | 3 | HG01515.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.199-2912_199-2911i others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023386 | ||||||
| chr6:105023387
|
T | A | 1 | a0001c0001t0004g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2911T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023387 | ||||||
| chr6:105023388
|
A | T | 1 | a0001c0001t0004g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2910A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023388 | ||||||
| chr6:105023394
|
A | AATTATAT others(3): Show |
4 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(1): Show | 4 | HG01515.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-2902_199-2901i others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023394 | |||||
| chr6:105023395
|
A | T | 1 | a0001c0001t0004g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.199-2903A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023395 | ||||||
| chr6:105023398
|
T | TA | 5 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(2): Show | 5 | HG01515.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2899dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023398 | |||||
| chr6:105023404
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-2894A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023404 | ||||||
| chr6:105023405
|
T | A | 17 | a0001c0001t0002g0124a0001c0001t0002g0129a0001c0001t0002g0200others(14): Show | 17 | HG00099.hp1 HG00423.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.199-2893T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023405 | ||||||
| chr6:105023405
|
T | TATATATA others(3): Show |
4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2893_199-2892i others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023405 | ||||||
| chr6:105023410
|
T | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2888T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023410 | ||||||
| chr6:105023410
|
TTA | T | 5 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2881_199-2880d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023410 | |||||
| chr6:105023412
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0177a0001c0001t0002g0160a0001c0001t0010g0121 | 3 | HG01358.hp1 HG01433.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.199-2880_199-2879i others(11): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023412 | |||||
| chr6:105023417
|
TAA | T | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(1): Show | 4 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-2880_199-2879d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023417 | ||||||
| chr6:105023418
|
A | ATATTATA others(42): Show |
1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.199-2880_199-2879i others(51): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023418 | ||||||
| chr6:105023419
|
A | T | 4 | a0001c0001t0002g0239a0001c0001t0004g0170a0001c0001t0006g0169others(1): Show | 4 | HG02976.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-2879A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023419 | ||||||
| chr6:105023420
|
T | A | 1 | a0001c0001t0004g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2878T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023420 | ||||||
| chr6:105023426
|
T | A | 1 | a0001c0001t0004g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-2872T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023426 | ||||||
| chr6:105023427
|
A | T | 2 | a0001c0001t0001g0193a0001c0001t0002g0014 | 2 | HG02074.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.199-2871A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023427 | ||||||
| chr6:105023428
|
A | AAAT | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2870_199-2869i others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023428 | ||||||
| chr6:105023429
|
T | A | 7 | a0001c0001t0002g0082a0001c0001t0002g0209a0001c0001t0002g0228others(4): Show | 7 | HG01993.hp2 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-2869T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023429 | ||||||
| chr6:105023429
|
T | TATATAAC others(71): Show |
5 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2869_199-2868i others(80): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023429 | ||||||
| chr6:105023432
|
T | TATATAAT others(7): Show |
1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.199-2864_199-2863i others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023432 | |||||
| chr6:105023433
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-2865A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023433 | ||||||
| chr6:105023434
|
T | A | 1 | a0001c0001t0004g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2864T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023434 | ||||||
| chr6:105023434
|
T | TTTTA | 5 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2863_199-2862i others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023434 | |||||
| chr6:105023434
|
TTA | T | 14 | a0001c0001t0001g0111a0001c0001t0002g0007a0001c0001t0002g0021others(11): Show | 14 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-2857_199-2856d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023434 | |||||
| chr6:105023435
|
T | A | 5 | a0001c0001t0004g0114a0001c0001t0007g0057a0001c0001t0013g0056others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2863T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023435 | ||||||
| chr6:105023436
|
A | ATATATAT others(2): Show |
29 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0131others(26): Show | 29 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.199-2856_199-2855i others(11): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023436 | |||||
| chr6:105023436
|
A | T | 1 | a0001c0001t0004g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199-2862A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023436 | ||||||
| chr6:105023441
|
T | A | 1 | a0001c0001t0004g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2857T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023441 | ||||||
| chr6:105023442
|
A | ATATTATA others(4): Show |
1 | a0001c0001t0001g0139 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.199-2856_199-2855i others(13): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023442 | ||||||
| chr6:105023442
|
A | C | 1 | a0001c0001t0004g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2856A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023442 | ||||||
| chr6:105023442
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-2856A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023442 | ||||||
| chr6:105023443
|
A | ACC | 5 | a0001c0001t0004g0114a0001c0001t0007g0057a0001c0001t0013g0056others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2855_199-2854i others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023443 | ||||||
| chr6:105023443
|
A | C | 1 | a0001c0001t0004g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2855A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023443 | ||||||
| chr6:105023443
|
A | T | 11 | a0001c0001t0002g0033a0001c0001t0002g0242a0001c0001t0003g0066others(8): Show | 11 | HG01358.hp2 HG01928.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-2855A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023443 | ||||||
| chr6:105023444
|
T | A | 7 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(4): Show | 7 | HG01928.hp1 HG01928.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-2854T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023444 | ||||||
| chr6:105023445
|
A | T | 2 | a0001c0001t0003g0066a0001c0001t0003g0208 | 2 | HG01928.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.199-2853A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023445 | ||||||
| chr6:105023446
|
T | TAATTATA others(89): Show |
1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-2851_199-2850i others(98): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023446 | |||||
| chr6:105023451
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.199-2847A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023451 | ||||||
| chr6:105023452
|
A | T | 6 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0007g0057others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-2846A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023452 | ||||||
| chr6:105023453
|
T | A | 4 | a0001c0001t0001g0232a0001c0001t0002g0229a0001c0001t0003g0231others(1): Show | 4 | NA18949.hp1 NA18952.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2845T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023453 | ||||||
| chr6:105023453
|
T | TA | 17 | a0001c0001t0001g0193a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 17 | HG02055.hp1 HG02074.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.199-2845_199-2844i others(3): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023453 | ||||||
| chr6:105023453
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0179a0001c0001t0002g0160 | 2 | HG00099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.199-2845_199-2844i others(14): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023453 | ||||||
| chr6:105023456
|
T | A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199-2842T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023456 | ||||||
| chr6:105023457
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.199-2841A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023457 | ||||||
| chr6:105023458
|
TTA | T | 21 | a0001c0001t0001g0111a0001c0001t0002g0007a0001c0001t0002g0021others(18): Show | 21 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.199-2833_199-2832d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023458 | |||||
| chr6:105023459
|
T | A | 6 | a0001c0001t0001g0179a0001c0001t0002g0160a0001c0001t0002g0239others(3): Show | 6 | HG00099.hp2 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-2839T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023459 | ||||||
| chr6:105023460
|
A | ATATAATA others(13): Show |
1 | a0001c0001t0004g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.199-2834_199-2833i others(22): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023460 | |||||
| chr6:105023460
|
A | ATATATAT others(2): Show |
24 | a0001c0001t0001g0131a0001c0001t0001g0146a0001c0001t0001g0155others(21): Show | 24 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.199-2832_199-2831i others(11): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023460 | |||||
| chr6:105023460
|
A | T | 6 | a0001c0001t0001g0168a0001c0001t0002g0239a0001c0001t0004g0153others(3): Show | 6 | HG02976.hp2 HG03486.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-2838A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023460 | ||||||
| chr6:105023466
|
A | ATATAATT others(80): Show |
1 | a0001c0001t0005g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.199-2832_199-2831i others(89): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023466 | ||||||
| chr6:105023466
|
A | G | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-2832A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023466 | ||||||
| chr6:105023466
|
A | T | 2 | a0001c0001t0001g0193a0001c0001t0002g0014 | 2 | HG02074.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.199-2832A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023466 | ||||||
| chr6:105023467
|
A | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(68): Show | 72 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.199-2831A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023467 | ||||||
| chr6:105023468
|
T | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.199-2830T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023468 | ||||||
| chr6:105023469
|
A | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.199-2829A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023469 | ||||||
| chr6:105023474
|
T | TATA | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-2823_199-2822i others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023474 | |||||
| chr6:105023474
|
T | TTA | 3 | a0001c0001t0002g0253a0001c0001t0005g0008a0002c0003t0002g0237 | 3 | HG03486.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.199-2824_199-2823i others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023474 | ||||||
| chr6:105023475
|
A | T | 10 | a0001c0001t0002g0253a0001c0001t0004g0113a0001c0001t0004g0114others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-2823A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023475 | ||||||
| chr6:105023476
|
A | T | 2 | a0001c0001t0001g0179a0001c0001t0002g0160 | 2 | HG00099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.199-2822A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023476 | ||||||
| chr6:105023477
|
T | A | 7 | a0001c0001t0001g0125a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG02027.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-2821T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023477 | ||||||
| chr6:105023477
|
T | TA | 86 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.199-2821_199-2820i others(3): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023477 | ||||||
| chr6:105023477
|
T | TATATAAC others(12): Show |
2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.199-2821_199-2820i others(21): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023477 | ||||||
| chr6:105023481
|
A | T | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2817A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023481 | ||||||
| chr6:105023482
|
T | TAAAA | 24 | a0001c0001t0001g0131a0001c0001t0001g0155a0001c0001t0001g0158others(21): Show | 24 | HG00558.hp1 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-2816_199-2815i others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023482 | ||||||
| chr6:105023482
|
T | TTA | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2809_199-2808d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023482 | |||||
| chr6:105023482
|
T | TTATATAA | 6 | a0001c0001t0001g0111a0001c0001t0002g0007a0001c0001t0003g0070others(3): Show | 6 | HG01891.hp1 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-2810_199-2809i others(9): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023482 | |||||
| chr6:105023482
|
TTA | T | 43 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0042others(40): Show | 43 | HG00323.hp1 HG01167.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.199-2809_199-2808d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023482 | |||||
| chr6:105023483
|
T | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(56): Show | 59 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.199-2815T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023483 | ||||||
| chr6:105023484
|
A | ATATAATA others(13): Show |
1 | a0001c0001t0001g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.199-2810_199-2809i others(22): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | ATATAATA others(35): Show |
1 | a0001c0001t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.199-2810_199-2809i others(44): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | ATATATAA others(15): Show |
29 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0051others(26): Show | 29 | HG00735.hp1 HG01106.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.199-2774_199-2753d others(24): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | ATATATAA others(39): Show |
7 | a0001c0001t0001g0055a0001c0001t0001g0232a0001c0001t0003g0072others(4): Show | 7 | HG01943.hp1 HG06807.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-2786_199-2785i others(48): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | ATATATAA others(61): Show |
1 | a0001c0001t0022g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.199-2786_199-2785i others(70): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | ATATATAA others(83): Show |
1 | a0001c0001t0003g0104 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.199-2786_199-2785i others(92): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | ATATATAA others(135): Show |
1 | a0001c0001t0003g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.199-2786_199-2785i others(144): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | ATATATAA others(85): Show |
1 | a0001c0001t0003g0087 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.199-2786_199-2785i others(94): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | ATATATAT others(2): Show |
20 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0133others(17): Show | 20 | HG00423.hp1 HG00642.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.199-2808_199-2807i others(11): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023484 | |||||
| chr6:105023484
|
A | T | 6 | a0001c0001t0001g0256a0001c0001t0002g0242a0001c0001t0004g0113others(3): Show | 6 | HG01358.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-2814A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023484 | ||||||
| chr6:105023485
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.199-2813T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023485 | ||||||
| chr6:105023485
|
TA | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.199-2812delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023485 | ||||||
| chr6:105023486
|
A | T | 1 | a0001c0001t0001g0130 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.199-2812A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023486 | ||||||
| chr6:105023488
|
ATAATATA others(6): Show |
A | 1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199-2807_199-2795d others(15): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023488 | |||||
| chr6:105023490
|
A | G | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-2808A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023490 | ||||||
| chr6:105023490
|
A | T | 2 | a0001c0001t0001g0193a0001c0001t0005g0040 | 2 | HG02074.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.199-2808A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023490 | ||||||
| chr6:105023491
|
A | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.199-2807A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023491 | ||||||
| chr6:105023492
|
T | A | 5 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(2): Show | 5 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2806T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023492 | ||||||
| chr6:105023492
|
T | TATATATA others(37): Show |
1 | a0001c0001t0002g0229 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.199-2786_199-2785i others(46): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023492 | |||||
| chr6:105023493
|
A | T | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0019g0202 | 3 | HG02572.hp1 HG02895.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.199-2805A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023493 | ||||||
| chr6:105023497
|
A | AACC | 30 | a0001c0001t0001g0111a0001c0001t0001g0131a0001c0001t0001g0155others(27): Show | 30 | HG00558.hp1 HG00735.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.199-2801_199-2800i others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023497 | ||||||
| chr6:105023497
|
ATAAT | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.199-2798_199-2795d others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023497 | |||||
| chr6:105023498
|
TA | T | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-2798delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023498 | |||||
| chr6:105023499
|
A | T | 6 | a0001c0001t0001g0179a0001c0001t0001g0241a0001c0001t0002g0160others(3): Show | 6 | HG00099.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-2799A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023499 | ||||||
| chr6:105023499
|
AAT | A | 3 | a0001c0001t0001g0134a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02572.hp1 HG02895.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.199-2798_199-2797d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023499 | ||||||
| chr6:105023500
|
A | T | 35 | a0001c0001t0001g0111a0001c0001t0001g0131a0001c0001t0001g0155others(32): Show | 35 | HG00558.hp1 HG00735.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.199-2798A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023500 | ||||||
| chr6:105023500
|
ATTATAT | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG02615.hp1 HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.199-2796_199-2791d others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023500 | |||||
| chr6:105023501
|
T | A | 31 | a0001c0001t0001g0111a0001c0001t0001g0131a0001c0001t0001g0155others(28): Show | 31 | HG00558.hp1 HG00735.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.199-2797T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023501 | ||||||
| chr6:105023501
|
T | TA | 13 | a0001c0001t0001g0179a0001c0001t0001g0256a0001c0001t0002g0160others(10): Show | 13 | HG00099.hp2 HG01358.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.199-2797_199-2796i others(3): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023501 | ||||||
| chr6:105023501
|
T | TATA | 21 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0252others(18): Show | 22 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.199-2797_199-2796i others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023501 | ||||||
| chr6:105023501
|
T | TATTATAT others(98): Show |
1 | a0001c0001t0001g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.199-2797_199-2796i others(107): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023501 | ||||||
| chr6:105023501
|
T | TTATATTA others(4): Show |
14 | a0001c0001t0001g0194a0001c0001t0001g0276a0001c0001t0002g0032others(11): Show | 14 | HG00099.hp1 HG00642.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.199-2796_199-2786d others(13): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023501 | |||||
| chr6:105023501
|
T | TTATATTT others(3): Show |
1 | a0001c0001t0002g0217 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.199-2791_199-2790i others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023501 | |||||
| chr6:105023505
|
A | T | 5 | a0001c0001t0001g0134a0001c0001t0001g0179a0001c0001t0002g0160others(2): Show | 5 | HG00099.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2793A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023505 | ||||||
| chr6:105023505
|
AT | A | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-2791delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023505 | |||||
| chr6:105023506
|
T | A | 4 | a0001c0001t0001g0134a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2792T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023506 | ||||||
| chr6:105023506
|
T | TAAAATA | 4 | a0001c0001t0001g0256a0001c0001t0002g0242a0001c0001t0004g0254others(1): Show | 4 | HG01358.hp2 HG02965.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2792_199-2791i others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023506 | ||||||
| chr6:105023506
|
T | TTA | 12 | a0001c0001t0001g0015a0001c0001t0001g0116a0001c0001t0001g0167others(9): Show | 12 | HG01515.hp2 HG01978.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.199-2787_199-2786d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023506 | |||||
| chr6:105023507
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.199-2791T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023507 | ||||||
| chr6:105023512
|
A | AT | 21 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0133others(18): Show | 21 | HG00423.hp1 HG00642.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.199-2786_199-2785i others(3): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023512 | ||||||
| chr6:105023512
|
A | ATTTT | 4 | a0001c0001t0001g0179a0001c0001t0002g0160a0001c0001t0004g0003others(1): Show | 4 | HG00099.hp2 HG02145.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2786_199-2785i others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023512 | ||||||
| chr6:105023513
|
A | T | 40 | a0001c0001t0001g0111a0001c0001t0001g0131a0001c0001t0001g0155others(37): Show | 40 | HG00558.hp1 HG00735.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.199-2785A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023513 | ||||||
| chr6:105023514
|
T | A | 3 | a0001c0001t0001g0193a0001c0001t0002g0014a0001c0001t0002g0218 | 3 | HG02074.hp1 HG02886.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.199-2784T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023514 | ||||||
| chr6:105023514
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG02615.hp1 HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.199-2784T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023514 | ||||||
| chr6:105023515
|
A | AT | 21 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0133others(18): Show | 21 | HG00423.hp1 HG00642.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.199-2782dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023515 | |||||
| chr6:105023515
|
A | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG02615.hp1 HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.199-2783A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023515 | ||||||
| chr6:105023515
|
A | T | 5 | a0001c0001t0002g0218a0001c0001t0007g0057a0001c0001t0013g0056others(2): Show | 5 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2783A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023515 | ||||||
| chr6:105023519
|
A | AACC | 4 | a0001c0001t0001g0256a0001c0001t0002g0242a0001c0001t0004g0254others(1): Show | 4 | HG01358.hp2 HG02965.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2779_199-2778i others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023519 | ||||||
| chr6:105023519
|
ATAAT | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG02615.hp1 HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.199-2776_199-2773d others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023519 | |||||
| chr6:105023520
|
TA | T | 4 | a0001c0001t0001g0193a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02074.hp1 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2776delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023520 | |||||
| chr6:105023522
|
A | T | 10 | a0001c0001t0001g0256a0001c0001t0002g0242a0001c0001t0004g0113others(7): Show | 10 | HG01358.hp2 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-2776A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023522 | ||||||
| chr6:105023522
|
AT | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(67): Show | 71 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.199-2774delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023522 | |||||
| chr6:105023523
|
T | A | 8 | a0001c0001t0001g0256a0001c0001t0002g0242a0001c0001t0004g0254others(5): Show | 8 | HG01358.hp2 HG02055.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-2775T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023523 | ||||||
| chr6:105023523
|
T | TA | 63 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0118others(60): Show | 63 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.199-2775_199-2774i others(3): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023523 | ||||||
| chr6:105023523
|
T | TATATAAC others(5): Show |
10 | a0001c0001t0001g0027a0001c0001t0002g0064a0001c0001t0002g0259others(7): Show | 10 | HG00323.hp1 HG03130.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-2775_199-2774i others(14): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023523 | ||||||
| chr6:105023523
|
T | TATATAAC others(30): Show |
1 | a0001c0001t0002g0023 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.199-2775_199-2774i others(39): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023523 | ||||||
| chr6:105023526
|
T | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2772T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023526 | ||||||
| chr6:105023527
|
A | T | 1 | a0001c0001t0002g0023 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.199-2771A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023527 | ||||||
| chr6:105023527
|
AT | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0123others(72): Show | 76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.199-2769delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023527 | |||||
| chr6:105023528
|
T | A | 5 | a0001c0001t0003g0149a0001c0001t0007g0057a0001c0001t0013g0056others(2): Show | 5 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2770T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023528 | ||||||
| chr6:105023528
|
T | TAATATA | 22 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0133others(19): Show | 22 | HG00423.hp1 HG00642.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.199-2770_199-2769i others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023528 | ||||||
| chr6:105023528
|
T | TTA | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.199-2765_199-2764d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(259): Show |
1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.199-2764_199-2763i others(268): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(174): Show |
1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.199-2764_199-2763i others(183): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(178): Show |
2 | a0001c0001t0002g0122a0001c0001t0009g0227 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.199-2764_199-2763i others(187): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(130): Show |
12 | a0001c0001t0002g0032a0001c0001t0002g0082a0001c0001t0002g0124others(9): Show | 12 | HG00099.hp1 HG00642.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-2764_199-2763i others(139): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(130): Show |
1 | a0001c0001t0004g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199-2764_199-2763i others(139): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(163): Show |
1 | a0001c0001t0002g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.199-2764_199-2763i others(172): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(295): Show |
1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.199-2764_199-2763i others(304): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(76): Show |
16 | a0001c0001t0001g0131a0001c0001t0001g0155a0001c0001t0001g0161others(13): Show | 16 | HG00558.hp1 HG00735.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.199-2764_199-2763i others(85): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023528
|
T | TTATATAT others(112): Show |
1 | a0001c0001t0001g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.199-2764_199-2763i others(121): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023528 | |||||
| chr6:105023533
|
T | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0117others(90): Show | 94 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.199-2765T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023533 | ||||||
| chr6:105023533
|
T | TATAATAT others(20): Show |
1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-2764_199-2763i others(29): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023533 | |||||
| chr6:105023533
|
T | TATAATAT others(6): Show |
1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.199-2764_199-2763i others(15): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023533 | |||||
| chr6:105023533
|
T | TATAATAT others(114): Show |
1 | a0001c0001t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.199-2764_199-2763i others(123): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023533 | |||||
| chr6:105023533
|
T | TATAATAT others(66): Show |
1 | a0001c0001t0001g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.199-2764_199-2763i others(75): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023533 | |||||
| chr6:105023533
|
T | TATATATT others(57): Show |
2 | a0001c0001t0001g0116a0001c0001t0001g0194 | 2 | HG04199.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.199-2764_199-2763i others(66): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023533 | |||||
| chr6:105023534
|
A | ATTTT | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0241others(3): Show | 6 | HG01515.hp1 HG01517.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-2764_199-2763i others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023534 | ||||||
| chr6:105023534
|
A | ATTTTAT | 9 | a0001c0001t0001g0179a0001c0001t0002g0009a0001c0001t0002g0010others(6): Show | 9 | HG00099.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-2764_199-2763i others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023534 | ||||||
| chr6:105023534
|
A | ATTTTATA others(6): Show |
9 | a0001c0001t0001g0111a0001c0001t0002g0007a0001c0001t0003g0070others(6): Show | 9 | HG01891.hp1 HG02976.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-2764_199-2763i others(15): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023534 | ||||||
| chr6:105023535
|
A | T | 18 | a0001c0001t0001g0027a0001c0001t0001g0256a0001c0001t0002g0021others(15): Show | 18 | HG00323.hp1 HG01358.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.199-2763A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023535 | ||||||
| chr6:105023536
|
T | A | 40 | a0001c0001t0001g0131a0001c0001t0001g0155a0001c0001t0001g0161others(37): Show | 40 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.199-2762T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023536 | ||||||
| chr6:105023537
|
A | T | 1 | a0001c0001t0002g0239 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.199-2761A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023537 | ||||||
| chr6:105023542
|
T | A | 13 | a0001c0001t0001g0179a0001c0001t0002g0009a0001c0001t0002g0010others(10): Show | 13 | HG00099.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.199-2756T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023542 | ||||||
| chr6:105023543
|
A | T | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2755A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023543 | ||||||
| chr6:105023544
|
A | ATTATAT | 3 | a0001c0001t0003g0074a0001c0001t0003g0075a0001c0001t0003g0079 | 3 | HG02083.hp2 NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.199-2753_199-2752i others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023544 | |||||
| chr6:105023545
|
TATATAAC others(3): Show |
T | 1 | a0001c0001t0004g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-2752_199-2743d others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023545 | ||||||
| chr6:105023550
|
A | T | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2748A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023550 | ||||||
| chr6:105023551
|
A | T | 49 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0131others(46): Show | 49 | HG00323.hp1 HG00558.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.199-2747A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023551 | ||||||
| chr6:105023552
|
C | A | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-2746C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023552 | ||||||
| chr6:105023552
|
C | T | 86 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0131others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.199-2746C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023552 | ||||||
| chr6:105023553
|
C | A | 87 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0131others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.199-2745C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023553 | ||||||
| chr6:105023557
|
A | AATATATA others(37): Show |
2 | a0001c0001t0001g0179a0001c0001t0002g0160 | 2 | HG00099.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.199-2741_199-2740i others(46): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023557 | ||||||
| chr6:105023557
|
A | AT | 22 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0001g0276others(19): Show | 22 | HG00099.hp1 HG00642.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.199-2740dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATAATTAT others(104): Show |
3 | a0001c0001t0003g0074a0001c0001t0003g0075a0001c0001t0003g0079 | 3 | HG02083.hp2 NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.199-2739_199-2738i others(113): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(170): Show |
1 | a0001c0001t0012g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(179): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(91): Show |
1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(100): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(57): Show |
5 | a0001c0001t0001g0238a0001c0001t0002g0252a0001c0001t0002g0253others(2): Show | 5 | HG02622.hp1 HG02717.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2736_199-2735i others(66): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(93): Show |
1 | a0001c0001t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(102): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(136): Show |
1 | a0001c0001t0001g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(145): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(66): Show |
78 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0039others(75): Show | 78 | HG00423.hp2 HG00735.hp1 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.199-2736_199-2735i others(75): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(100): Show |
14 | a0001c0001t0001g0223a0001c0001t0002g0199a0001c0001t0002g0210others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-2736_199-2735i others(109): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(170): Show |
1 | a0001c0001t0001g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(179): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(136): Show |
48 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0123others(45): Show | 48 | HG00140.hp1 HG00140.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.199-2736_199-2735i others(145): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(172): Show |
1 | a0001c0001t0001g0222 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(181): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(208): Show |
1 | a0001c0001t0002g0219 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(217): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(93): Show |
1 | a0001c0001t0002g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(102): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(102): Show |
1 | a0001c0001t0002g0229 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(111): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(138): Show |
1 | a0001c0001t0005g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(147): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(93): Show |
1 | a0001c0001t0002g0214 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(102): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(172): Show |
1 | a0001c0001t0001g0127 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(181): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(126): Show |
1 | a0001c0001t0003g0149 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(135): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(134): Show |
1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(143): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(59): Show |
1 | a0001c0001t0002g0024 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(68): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(64): Show |
1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(73): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATATTA others(120): Show |
1 | a0001c0001t0001g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.199-2736_199-2735i others(129): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATATTATA others(46): Show |
1 | a0001c0001t0002g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-2738_199-2737i others(55): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATTATATA others(3): Show |
5 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(2): Show | 5 | HG02559.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2740_199-2739i others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATTT | 36 | a0001c0001t0001g0111a0001c0001t0001g0131a0001c0001t0001g0155others(33): Show | 36 | HG00558.hp1 HG00735.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.199-2740_199-2739i others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATTTTATA others(66): Show |
2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.199-2740_199-2739i others(75): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | ATTTTATA others(32): Show |
8 | a0001c0001t0001g0027a0001c0001t0002g0259a0001c0001t0003g0267others(5): Show | 8 | HG00323.hp1 HG03130.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-2740_199-2739i others(41): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023557 | |||||
| chr6:105023557
|
A | T | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0004g0003others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2741A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023557 | ||||||
| chr6:105023560
|
T | TA | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2737dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023560 | |||||
| chr6:105023561
|
A | AT | 21 | a0001c0001t0001g0002a0001c0001t0001g0117a0001c0001t0001g0125others(18): Show | 22 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.199-2736dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023561 | |||||
| chr6:105023561
|
A | ATTATATA others(346): Show |
1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-2736_199-2735i others(355): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023561 | |||||
| chr6:105023561
|
A | G | 3 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0052 | 3 | HG01891.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.199-2737A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023561 | ||||||
| chr6:105023561
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199-2737A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023561 | ||||||
| chr6:105023562
|
T | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2736T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023562 | ||||||
| chr6:105023562
|
TATATAAT others(28): Show |
T | 2 | a0001c0001t0001g0018a0001c0001t0001g0042 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-2735_199-2701d others(37): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023562 | ||||||
| chr6:105023565
|
A | T | 9 | a0001c0001t0001g0256a0001c0001t0002g0062a0001c0001t0002g0063others(6): Show | 9 | HG01358.hp2 HG02965.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-2733A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023565 | ||||||
| chr6:105023567
|
A | ATTATATA others(29): Show |
1 | a0001c0001t0002g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.199-2731_199-2730i others(38): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023567 | ||||||
| chr6:105023567
|
A | T | 9 | a0001c0001t0001g0256a0001c0001t0002g0062a0001c0001t0002g0063others(6): Show | 9 | HG01358.hp2 HG02965.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-2731A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023567 | ||||||
| chr6:105023568
|
A | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0117a0001c0001t0001g0125others(23): Show | 27 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.199-2730A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023568 | ||||||
| chr6:105023569
|
T | A | 147 | a0001c0001t0001g0015a0001c0001t0001g0111a0001c0001t0001g0115others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.199-2729T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023569 | ||||||
| chr6:105023570
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199-2728A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023570 | ||||||
| chr6:105023575
|
T | A | 3 | a0001c0001t0002g0021a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02572.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.199-2723T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023575 | ||||||
| chr6:105023578
|
T | A | 1 | a0001c0001t0002g0239 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.199-2720T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023578 | ||||||
| chr6:105023584
|
T | C | 1 | a0001c0001t0004g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-2714T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023584 | ||||||
| chr6:105023584
|
T | TTA | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(1): Show | 4 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-2706_199-2705d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023584 | |||||
| chr6:105023585
|
T | A | 1 | a0001c0001t0002g0239 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.199-2713T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023585 | ||||||
| chr6:105023585
|
T | TATATATT others(54): Show |
2 | a0001c0001t0002g0047a0001c0001t0007g0048 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.199-2707_199-2706i others(63): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023585 | |||||
| chr6:105023585
|
T | TATATATT others(56): Show |
11 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0004g0001others(8): Show | 12 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-2707_199-2706i others(65): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023585 | |||||
| chr6:105023585
|
T | TATATATT others(164): Show |
4 | a0001c0001t0006g0172a0001c0001t0006g0173a0001c0001t0006g0174others(1): Show | 4 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2707_199-2706i others(173): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023585 | |||||
| chr6:105023592
|
A | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0115others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.199-2706A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023592 | ||||||
| chr6:105023594
|
T | A | 3 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171 | 3 | HG02976.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.199-2704T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023594 | ||||||
| chr6:105023595
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199-2703A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023595 | ||||||
| chr6:105023596
|
T | A | 3 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171 | 3 | HG02976.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.199-2702T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023596 | ||||||
| chr6:105023598
|
T | C | 2 | a0001c0001t0004g0113a0001c0001t0004g0114 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.199-2700T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023598 | ||||||
| chr6:105023601
|
A | ATAAAATA others(60): Show |
1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.199-2642_199-2641i others(69): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023601 | |||||
| chr6:105023601
|
A | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0117a0001c0001t0001g0125 | 3 | HG02027.hp2 HG03654.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.199-2697A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023601 | ||||||
| chr6:105023603
|
A | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0117a0001c0001t0001g0125others(12): Show | 16 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.199-2695A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023603 | ||||||
| chr6:105023604
|
A | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0007g0057others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-2694A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023604 | ||||||
| chr6:105023605
|
A | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0042others(54): Show | 57 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.199-2693A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023605 | ||||||
| chr6:105023614
|
T | A | 16 | a0001c0001t0002g0239a0001c0001t0002g0249a0001c0001t0002g0250others(13): Show | 17 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.199-2684T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023614 | ||||||
| chr6:105023621
|
T | A | 16 | a0001c0001t0002g0239a0001c0001t0002g0249a0001c0001t0002g0250others(13): Show | 17 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.199-2677T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023621 | ||||||
| chr6:105023621
|
T | TATATATA others(20): Show |
3 | a0001c0001t0002g0242a0001c0001t0004g0254a0001c0001t0007g0255 | 3 | HG01358.hp2 HG02965.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.199-2671_199-2670i others(29): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023621 | |||||
| chr6:105023626
|
A | ATTTTATA others(136): Show |
1 | a0001c0001t0001g0125 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.199-2643_199-2642i others(145): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023626 | |||||
| chr6:105023628
|
T | A | 71 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0001g0232others(68): Show | 72 | HG00323.hp2 HG00423.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.199-2670T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023628 | ||||||
| chr6:105023628
|
T | TTTATATA others(92): Show |
3 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171 | 3 | HG02976.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.199-2662_199-2661i others(101): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023628 | |||||
| chr6:105023629
|
T | A | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-2669T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023629 | ||||||
| chr6:105023635
|
A | G | 2 | a0001c0001t0004g0113a0001c0001t0004g0114 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.199-2663A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023635 | ||||||
| chr6:105023637
|
A | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0004g0097 | 3 | HG01891.hp2 HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.199-2661A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023637 | ||||||
| chr6:105023638
|
TAAAA | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0004g0097 | 3 | HG01891.hp2 HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.199-2659_199-2656d others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023638 | ||||||
| chr6:105023641
|
A | T | 5 | a0001c0001t0003g0075a0001c0001t0003g0079a0001c0001t0005g0040others(2): Show | 5 | HG00423.hp2 HG01243.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2657A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023641 | ||||||
| chr6:105023649
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.199-2649A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023649 | ||||||
| chr6:105023650
|
T | TATATAAT others(162): Show |
1 | a0001c0001t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.199-2643_199-2642i others(171): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105023650 | |||||
| chr6:105023659
|
A | T | 1 | a0001c0001t0002g0064 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.199-2639A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023659 | ||||||
| chr6:105023661
|
T | A | 5 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0007g0057others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2637T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023661 | ||||||
| chr6:105023710
|
G | A | 7 | a0001c0001t0004g0170a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-2588G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023710 | ||||||
| chr6:105023793
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.199-2505G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105023793 | ||||||
| chr6:105024058
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.199-2240C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024058 | ||||||
| chr6:105024138
|
G | A | 25 | a0001c0001t0002g0082a0001c0001t0002g0122a0001c0001t0002g0124others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.199-2160G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024138 | ||||||
| chr6:105024194
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0003g0274 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.199-2104G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024194 | ||||||
| chr6:105024246
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.199-2052C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024246 | ||||||
| chr6:105024298
|
T | TA | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.199-1999dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105024298 | |||||
| chr6:105024353
|
A | T | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-1945A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024353 | ||||||
| chr6:105024445
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0116others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.199-1853G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024445 | ||||||
| chr6:105024501
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.199-1797G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024501 | ||||||
| chr6:105024525
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.199-1773A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024525 | ||||||
| chr6:105024716
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.199-1582C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024716 | ||||||
| chr6:105024895
|
A | G | 1 | a0001c0001t0004g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199-1403A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105024895 | ||||||
| chr6:105025032
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0042 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-1266C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105025032 | ||||||
| chr6:105025050
|
C | T | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199-1248C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105025050 | ||||||
| chr6:105025464
|
T | A | 1 | a0001c0001t0003g0096 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.199-834T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105025464 | ||||||
| chr6:105025543
|
A | G | 3 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0052 | 3 | HG01891.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.199-755A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105025543 | ||||||
| chr6:105025608
|
T | C | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-690T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105025608 | ||||||
| chr6:105025695
|
T | C | 1 | a0001c0001t0005g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.199-603T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105025695 | ||||||
| chr6:105025771
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0011g0076 | 2 | NA18946.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.199-527C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105025771 | ||||||
| chr6:105025807
|
CT | C | 5 | a0001c0001t0002g0110a0001c0001t0003g0070a0001c0001t0003g0269others(2): Show | 5 | HG01167.hp1 NA18939.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-480delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 105025807 | |||||
| chr6:105026064
|
T | A | 8 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(5): Show | 8 | HG01515.hp2 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-234T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 2/3 | chr6 | 105026064 | ||||||
| chr6:105026558
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.383+76G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105026558 | ||||||
| chr6:105026763
|
A | C | 5 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG03195.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+281A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105026763 | ||||||
| chr6:105026765
|
G | A | 1 | a0001c0001t0003g0080 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.383+283G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105026765 | ||||||
| chr6:105027022
|
A | G | 9 | a0001c0001t0001g0118a0001c0001t0001g0125a0001c0001t0001g0137others(6): Show | 9 | HG00558.hp1 HG02027.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+540A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027022 | ||||||
| chr6:105027198
|
G | A | 2 | a0001c0001t0003g0070a0001c0001t0003g0073 | 2 | NA18957.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.383+716G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027198 | ||||||
| chr6:105027234
|
C | T | 23 | a0001c0001t0002g0239a0001c0001t0002g0242a0001c0001t0002g0249others(20): Show | 24 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+752C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027234 | ||||||
| chr6:105027379
|
T | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0091a0001c0001t0001g0115others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.383+897T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027379 | ||||||
| chr6:105027390
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383+908T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027390 | ||||||
| chr6:105027561
|
A | G | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.383+1079A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027561 | ||||||
| chr6:105027599
|
A | C | 1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.383+1117A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027599 | ||||||
| chr6:105027699
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.383+1217C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027699 | ||||||
| chr6:105027755
|
A | G | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.383+1273A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027755 | ||||||
| chr6:105027811
|
A | G | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.383+1329A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105027811 | ||||||
| chr6:105028025
|
G | A | 2 | a0001c0001t0004g0240a0001c0001t0004g0245 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.383+1543G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105028025 | ||||||
| chr6:105028059
|
C | A | 1 | a0001c0001t0014g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.383+1577C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105028059 | ||||||
| chr6:105028073
|
T | C | 1 | a0001c0001t0027g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.383+1591T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105028073 | ||||||
| chr6:105028516
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.383+2034G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105028516 | ||||||
| chr6:105028740
|
G | C | 1 | a0001c0001t0004g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.383+2258G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105028740 | ||||||
| chr6:105028878
|
C | G | 5 | a0001c0001t0003g0086a0001c0001t0003g0093a0001c0001t0011g0076others(2): Show | 5 | HG02027.hp1 HG02074.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+2396C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105028878 | ||||||
| chr6:105029007
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.383+2525A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105029007 | ||||||
| chr6:105029408
|
T | C | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+2926T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105029408 | ||||||
| chr6:105029505
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.383+3023G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105029505 | ||||||
| chr6:105029821
|
A | G | 9 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(6): Show | 9 | HG01515.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+3339A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105029821 | ||||||
| chr6:105029922
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.383+3440C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105029922 | ||||||
| chr6:105029926
|
G | A | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+3444G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105029926 | ||||||
| chr6:105029985
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.383+3503G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105029985 | ||||||
| chr6:105030008
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.383+3526A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030008 | ||||||
| chr6:105030239
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.383+3757A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030239 | ||||||
| chr6:105030290
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.383+3808C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030290 | ||||||
| chr6:105030416
|
A | C | 1 | a0001c0001t0003g0073 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.383+3934A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030416 | ||||||
| chr6:105030520
|
C | A | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383+4038C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030520 | ||||||
| chr6:105030592
|
C | CT | 19 | a0001c0001t0001g0026a0001c0001t0001g0125a0001c0001t0001g0146others(16): Show | 19 | HG01074.hp2 HG01255.hp2 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.383+4131dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105030592 | |||||
| chr6:105030592
|
CT | C | 61 | a0001c0001t0001g0039a0001c0001t0001g0167a0001c0001t0001g0181others(58): Show | 62 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.383+4131delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105030592 | |||||
| chr6:105030612
|
T | C | 11 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0002g0236others(8): Show | 11 | HG01515.hp2 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.383+4130T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030612 | ||||||
| chr6:105030618
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.383+4136A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030618 | ||||||
| chr6:105030635
|
C | T | 5 | a0001c0001t0003g0086a0001c0001t0003g0093a0001c0001t0011g0076others(2): Show | 5 | HG02027.hp1 HG02074.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+4153C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030635 | ||||||
| chr6:105030781
|
A | T | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.383+4299A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105030781 | ||||||
| chr6:105031028
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383+4546G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105031028 | ||||||
| chr6:105031052
|
C | A | 76 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0001g0223others(73): Show | 77 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.383+4570C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105031052 | ||||||
| chr6:105031134
|
T | G | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.383+4652T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105031134 | ||||||
| chr6:105031146
|
AT | A | 39 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0001g0223others(36): Show | 39 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.383+4668delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105031146 | |||||
| chr6:105031542
|
T | C | 14 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(11): Show | 14 | HG00735.hp1 HG01243.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.383+5060T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105031542 | ||||||
| chr6:105031546
|
T | C | 1 | a0001c0001t0004g0254 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.383+5064T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105031546 | ||||||
| chr6:105031653
|
C | T | 18 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(15): Show | 18 | HG00735.hp1 HG01243.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.383+5171C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105031653 | ||||||
| chr6:105031683
|
A | G | 64 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0001g0223others(61): Show | 65 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.383+5201A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105031683 | ||||||
| chr6:105031777
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0009g0017 | 3 | HG02976.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.383+5295C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105031777 | ||||||
| chr6:105032038
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.383+5556A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032038 | ||||||
| chr6:105032148
|
A | G | 4 | a0001c0001t0007g0057a0001c0001t0013g0056a0001c0001t0013g0058others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+5666A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032148 | ||||||
| chr6:105032433
|
T | A | 3 | a0001c0001t0008g0132a0001c0001t0008g0147a0001c0001t0008g0157 | 3 | NA18948.hp2 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.383+5951T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032433 | ||||||
| chr6:105032574
|
A | T | 23 | a0001c0001t0002g0239a0001c0001t0002g0242a0001c0001t0002g0249others(20): Show | 24 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+6092A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032574 | ||||||
| chr6:105032728
|
A | G | 1 | a0001c0001t0003g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.383+6246A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032728 | ||||||
| chr6:105032732
|
A | T | 23 | a0001c0001t0002g0239a0001c0001t0002g0242a0001c0001t0002g0249others(20): Show | 24 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+6250A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032732 | ||||||
| chr6:105032733
|
T | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0256a0001c0001t0002g0110others(12): Show | 15 | HG00423.hp2 HG02074.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.383+6251T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032733 | ||||||
| chr6:105032734
|
T | A | 1 | a0001c0001t0003g0101 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.383+6252T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032734 | ||||||
| chr6:105032809
|
A | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | NA18950.hp1 NA18965.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+6327A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032809 | ||||||
| chr6:105032819
|
A | T | 255 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.383+6337A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032819 | ||||||
| chr6:105032850
|
T | C | 23 | a0001c0001t0002g0239a0001c0001t0002g0242a0001c0001t0002g0249others(20): Show | 24 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+6368T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032850 | ||||||
| chr6:105032941
|
G | A | 23 | a0001c0001t0002g0239a0001c0001t0002g0242a0001c0001t0002g0249others(20): Show | 24 | HG00323.hp2 HG01074.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+6459G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032941 | ||||||
| chr6:105032962
|
A | G | 1 | a0001c0001t0003g0104 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.383+6480A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032962 | ||||||
| chr6:105032996
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.383+6514C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105032996 | ||||||
| chr6:105033045
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.383+6563A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033045 | ||||||
| chr6:105033419
|
T | A | 1 | a0001c0001t0015g0162 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.383+6937T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033419 | ||||||
| chr6:105033507
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.383+7025C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033507 | ||||||
| chr6:105033540
|
G | C | 1 | a0001c0001t0005g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383+7058G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033540 | ||||||
| chr6:105033651
|
C | G | 1 | a0001c0001t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.383+7169C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033651 | ||||||
| chr6:105033661
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.383+7179A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033661 | ||||||
| chr6:105033667
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383+7185A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033667 | ||||||
| chr6:105033680
|
A | G | 3 | a0001c0001t0002g0236a0001c0001t0004g0003a0001c0001t0004g0004 | 3 | HG01515.hp2 HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.383+7198A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033680 | ||||||
| chr6:105033773
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.383+7291T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033773 | ||||||
| chr6:105033818
|
T | A | 6 | a0001c0001t0002g0007a0001c0001t0002g0021a0001c0001t0002g0047others(3): Show | 6 | HG02615.hp1 HG03225.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+7336T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105033818 | ||||||
| chr6:105034193
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0002g0064 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.383+7711T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105034193 | ||||||
| chr6:105034252
|
A | G | 1 | a0001c0001t0003g0268 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.383+7770A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105034252 | ||||||
| chr6:105034343
|
C | G | 3 | a0001c0001t0013g0056a0001c0001t0013g0058a0001c0001t0014g0059 | 3 | HG02055.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.383+7861C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105034343 | ||||||
| chr6:105034374
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.383+7892C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105034374 | ||||||
| chr6:105034617
|
C | A | 1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.383+8135C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105034617 | ||||||
| chr6:105034662
|
AC | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | NA18950.hp1 NA18965.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+8182delC | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105034662 | |||||
| chr6:105034718
|
A | C | 3 | a0001c0001t0013g0056a0001c0001t0013g0058a0001c0001t0014g0059 | 3 | HG02055.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.383+8236A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105034718 | ||||||
| chr6:105034783
|
A | G | 2 | a0001c0001t0003g0088a0001c0001t0003g0096 | 2 | NA19011.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.383+8301A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105034783 | ||||||
| chr6:105034959
|
G | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.383+8477G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105034959 | ||||||
| chr6:105035052
|
A | C | 2 | a0001c0001t0013g0056a0001c0001t0013g0058 | 2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.383+8570A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105035052 | ||||||
| chr6:105035337
|
C | T | 1 | a0001c0001t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.383+8855C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105035337 | ||||||
| chr6:105035452
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.383+8970A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105035452 | ||||||
| chr6:105035755
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.383+9273G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105035755 | ||||||
| chr6:105036000
|
G | A | 1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.383+9518G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036000 | ||||||
| chr6:105036134
|
C | T | 3 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215 | 3 | HG02132.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.383+9652C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036134 | ||||||
| chr6:105036323
|
A | G | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+9841A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036323 | ||||||
| chr6:105036628
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.383+10146C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036628 | ||||||
| chr6:105036638
|
G | A | 1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.383+10156G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036638 | ||||||
| chr6:105036652
|
C | CTT | 216 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.383+10170_383+1017 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036652 | ||||||
| chr6:105036652
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.383+10170C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036652 | ||||||
| chr6:105036688
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.383+10206G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036688 | ||||||
| chr6:105036922
|
T | C | 1 | a0001c0001t0003g0268 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.383+10440T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105036922 | ||||||
| chr6:105036958
|
TTAAG | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0042others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.383+10479_383+1048 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105036958 | |||||
| chr6:105037022
|
C | T | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+10540C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037022 | ||||||
| chr6:105037023
|
G | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.383+10541G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037023 | ||||||
| chr6:105037138
|
A | G | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+10656A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037138 | ||||||
| chr6:105037162
|
TTTTGTTA others(27): Show |
T | 1 | a0001c0001t0003g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.383+10715_383+1074 others(38): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105037162 | |||||
| chr6:105037205
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.383+10723T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037205 | ||||||
| chr6:105037468
|
C | T | 2 | a0001c0001t0004g0060a0001c0001t0025g0112 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.383+10986C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037468 | ||||||
| chr6:105037512
|
T | C | 1 | a0001c0001t0023g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.383+11030T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037512 | ||||||
| chr6:105037520
|
C | CT | 8 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(5): Show | 8 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.383+11048dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105037520 | |||||
| chr6:105037684
|
AT | A | 8 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0002g0021others(5): Show | 8 | HG02615.hp1 HG02615.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.383+11211delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105037684 | |||||
| chr6:105037769
|
C | T | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0208 | 3 | HG01928.hp1 HG01928.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.383+11287C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037769 | ||||||
| chr6:105037802
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG02723.hp1 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+11320C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037802 | ||||||
| chr6:105037927
|
A | G | 20 | a0001c0001t0001g0051a0001c0001t0001g0111a0001c0001t0001g0167others(17): Show | 20 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.383+11445A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037927 | ||||||
| chr6:105037928
|
T | C | 37 | a0001c0001t0001g0181a0001c0001t0001g0223a0001c0001t0002g0032others(34): Show | 37 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.383+11446T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105037928 | ||||||
| chr6:105038418
|
C | T | 8 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(5): Show | 8 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.383+11936C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105038418 | ||||||
| chr6:105038538
|
G | C | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+12056G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105038538 | ||||||
| chr6:105038568
|
T | C | 2 | a0001c0001t0004g0060a0001c0001t0025g0112 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.383+12086T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105038568 | ||||||
| chr6:105038645
|
G | A | 1 | a0001c0001t0022g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.383+12163G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105038645 | ||||||
| chr6:105038773
|
A | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0111a0001c0001t0001g0167others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+12291A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105038773 | ||||||
| chr6:105038774
|
C | G | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+12292C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105038774 | ||||||
| chr6:105039587
|
C | G | 1 | a0001c0001t0002g0200 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.383+13105C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105039587 | ||||||
| chr6:105039588
|
A | AGCCACTT others(71): Show |
1 | a0001c0001t0002g0200 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.383+13106_383+1310 others(82): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105039588 | ||||||
| chr6:105039648
|
T | A | 1 | a0001c0001t0003g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.383+13166T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105039648 | ||||||
| chr6:105040128
|
G | A | 1 | a0001c0001t0003g0109 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.383+13646G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105040128 | ||||||
| chr6:105040131
|
A | G | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.383+13649A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105040131 | ||||||
| chr6:105040415
|
TCTC | T | 8 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(5): Show | 8 | HG02559.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.383+13937_383+1393 others(7): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105040415 | |||||
| chr6:105040607
|
CA | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0139a0001c0001t0003g0088others(1): Show | 4 | HG02027.hp2 NA19011.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+14133delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105040607 | |||||
| chr6:105040745
|
A | G | 1 | a0001c0001t0003g0267 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.383+14263A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105040745 | ||||||
| chr6:105040844
|
AAAG | A | 6 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(3): Show | 6 | HG02559.hp2 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+14367_383+1436 others(7): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105040844 | |||||
| chr6:105040860
|
TA | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.383+14379delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105040860 | ||||||
| chr6:105040907
|
C | A | 217 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.383+14425C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105040907 | ||||||
| chr6:105041077
|
A | AT | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+14609dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105041077 | |||||
| chr6:105041191
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.383+14709T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105041191 | ||||||
| chr6:105041192
|
G | A | 26 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0111others(23): Show | 26 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.383+14710G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105041192 | ||||||
| chr6:105041281
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG02723.hp1 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+14799G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105041281 | ||||||
| chr6:105041309
|
T | C | 41 | a0001c0001t0001g0055a0001c0001t0001g0181a0001c0001t0001g0223others(38): Show | 41 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.383+14827T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105041309 | ||||||
| chr6:105041334
|
T | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0095a0001c0001t0004g0240others(8): Show | 12 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.383+14852T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105041334 | ||||||
| chr6:105041885
|
C | T | 97 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0041others(94): Show | 98 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.383+15403C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105041885 | ||||||
| chr6:105041926
|
C | T | 4 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0014others(1): Show | 4 | HG02559.hp2 HG02886.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+15444C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105041926 | ||||||
| chr6:105042100
|
A | C | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+15618A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042100 | ||||||
| chr6:105042269
|
A | T | 61 | a0001c0001t0001g0051a0001c0001t0001g0111a0001c0001t0001g0115others(58): Show | 62 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.383+15787A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042269 | ||||||
| chr6:105042280
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.383+15798A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042280 | ||||||
| chr6:105042319
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383+15837C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042319 | ||||||
| chr6:105042638
|
T | G | 3 | a0001c0001t0007g0006a0001c0001t0007g0057a0001c0001t0007g0255 | 3 | HG02109.hp1 HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.383+16156T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042638 | ||||||
| chr6:105042734
|
T | G | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+16252T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042734 | ||||||
| chr6:105042824
|
C | T | 8 | a0001c0001t0001g0123a0001c0001t0001g0152a0001c0001t0001g0158others(5): Show | 8 | HG00140.hp1 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.383+16342C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042824 | ||||||
| chr6:105042865
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.383+16383T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042865 | ||||||
| chr6:105042933
|
T | C | 3 | a0001c0001t0001g0055a0001c0001t0004g0003a0001c0001t0004g0053 | 3 | HG03041.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.383+16451T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105042933 | ||||||
| chr6:105043036
|
G | A | 1 | a0001c0001t0004g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.383+16554G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043036 | ||||||
| chr6:105043090
|
T | C | 8 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0103others(5): Show | 8 | NA18939.hp2 NA18947.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.383+16608T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043090 | ||||||
| chr6:105043278
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.383+16796C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043278 | ||||||
| chr6:105043279
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0168a0001c0001t0001g0216 | 3 | HG00140.hp2 HG01069.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.383+16797G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043279 | ||||||
| chr6:105043341
|
C | CA | 9 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(6): Show | 9 | HG00323.hp2 HG01074.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.383+16890dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CA | C | 25 | a0001c0001t0002g0016a0001c0001t0002g0020a0001c0001t0002g0021others(22): Show | 25 | HG01169.hp2 HG01515.hp2 HG02293.hp1 others(22): Show |
intron_variant | MODIFIER | c.383+16890delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CAAA | C | 10 | a0001c0001t0001g0138a0001c0001t0004g0028a0001c0001t0004g0053others(7): Show | 10 | HG01891.hp1 HG02083.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.383+16888_383+1689 others(7): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CAAAA | C | 44 | a0001c0001t0001g0055a0001c0001t0001g0098a0001c0001t0001g0111others(41): Show | 45 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.383+16887_383+1689 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CAAAAA | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.383+16886_383+1689 others(9): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CAAAAAA | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0181others(4): Show | 7 | HG00735.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+16885_383+1689 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CAAAAAAA others(4): Show |
C | 12 | a0001c0001t0002g0145a0001c0001t0002g0209a0001c0001t0002g0210others(9): Show | 12 | HG00423.hp1 HG00558.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.383+16880_383+1689 others(15): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.383+16879_383+1689 others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CAAAAAAA others(10): Show |
C | 60 | a0001c0001t0001g0258a0001c0001t0003g0065a0001c0001t0003g0066others(57): Show | 60 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.383+16874_383+1689 others(21): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043341
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+16871_383+1689 others(24): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105043341 | |||||
| chr6:105043367
|
A | G | 3 | a0001c0001t0008g0132a0001c0001t0008g0147a0001c0001t0008g0157 | 3 | NA18948.hp2 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.383+16885A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043367 | ||||||
| chr6:105043376
|
A | G | 4 | a0001c0001t0004g0097a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+16894A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043376 | ||||||
| chr6:105043388
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.383+16906A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043388 | ||||||
| chr6:105043388
|
A | T | 5 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+16906A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043388 | ||||||
| chr6:105043443
|
A | T | 1 | a0001c0001t0004g0004 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.383+16961A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043443 | ||||||
| chr6:105043501
|
C | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.383+17019C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043501 | ||||||
| chr6:105043649
|
C | G | 2 | a0001c0001t0004g0060a0001c0001t0025g0112 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.383+17167C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043649 | ||||||
| chr6:105043766
|
A | C | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+17284A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043766 | ||||||
| chr6:105043880
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.383+17398G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043880 | ||||||
| chr6:105043928
|
A | G | 1 | a0001c0001t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.383+17446A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043928 | ||||||
| chr6:105043983
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.383+17501A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105043983 | ||||||
| chr6:105044058
|
C | T | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+17576C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105044058 | ||||||
| chr6:105044131
|
T | A | 1 | a0001c0001t0004g0004 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.383+17649T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105044131 | ||||||
| chr6:105044330
|
A | G | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+17848A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105044330 | ||||||
| chr6:105044588
|
A | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0023g0050others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+18106A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105044588 | ||||||
| chr6:105044594
|
A | G | 1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.383+18112A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105044594 | ||||||
| chr6:105044852
|
T | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(181): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.383+18370T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105044852 | ||||||
| chr6:105044862
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(181): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.383+18380A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105044862 | ||||||
| chr6:105045180
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(181): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.383+18698A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045180 | ||||||
| chr6:105045200
|
A | G | 1 | a0001c0001t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.383+18718A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045200 | ||||||
| chr6:105045284
|
G | GT | 27 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0055others(24): Show | 27 | HG00642.hp2 HG00735.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.383+18821dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105045284 | |||||
| chr6:105045284
|
G | GTT | 14 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(11): Show | 14 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.383+18820_383+1882 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105045284 | |||||
| chr6:105045373
|
G | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.383+18891G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045373 | ||||||
| chr6:105045478
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.383+18996G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045478 | ||||||
| chr6:105045547
|
A | T | 61 | a0001c0001t0001g0258a0001c0001t0002g0124a0001c0001t0003g0065others(58): Show | 61 | HG00423.hp2 HG01069.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.383+19065A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045547 | ||||||
| chr6:105045854
|
T | C | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+19372T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045854 | ||||||
| chr6:105045885
|
TG | T | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0208 | 3 | HG01928.hp1 HG01928.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.383+19404delG | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045885 | ||||||
| chr6:105045887
|
T | C | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0208 | 3 | HG01928.hp1 HG01928.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.383+19405T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045887 | ||||||
| chr6:105045888
|
G | A | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0208 | 3 | HG01928.hp1 HG01928.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.383+19406G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105045888 | ||||||
| chr6:105046124
|
A | G | 1 | a0001c0001t0004g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.383+19642A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046124 | ||||||
| chr6:105046155
|
A | G | 3 | a0001c0001t0008g0132a0001c0001t0008g0147a0001c0001t0008g0157 | 3 | NA18948.hp2 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.383+19673A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046155 | ||||||
| chr6:105046183
|
C | T | 2 | a0001c0001t0014g0059a0001c0001t0014g0235 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383+19701C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046183 | ||||||
| chr6:105046280
|
C | G | 20 | a0001c0001t0001g0167a0001c0001t0004g0001a0001c0001t0004g0003others(17): Show | 21 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.383+19798C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046280 | ||||||
| chr6:105046339
|
C | A | 1 | a0001c0001t0003g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.383+19857C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046339 | ||||||
| chr6:105046494
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | NA18959.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.383+20012T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046494 | ||||||
| chr6:105046825
|
G | A | 4 | a0001c0001t0004g0097a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+20343G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046825 | ||||||
| chr6:105046903
|
G | C | 1 | a0001c0001t0003g0087 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.383+20421G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046903 | ||||||
| chr6:105046958
|
T | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0140a0001c0001t0001g0163 | 3 | HG01074.hp2 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.383+20476T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046958 | ||||||
| chr6:105046959
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0140a0001c0001t0001g0163 | 3 | HG01074.hp2 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.383+20477C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046959 | ||||||
| chr6:105046960
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0140a0001c0001t0001g0163 | 3 | HG01074.hp2 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.383+20478C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105046960 | ||||||
| chr6:105047130
|
C | T | 2 | a0001c0001t0004g0003a0001c0001t0004g0053 | 2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.383+20648C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047130 | ||||||
| chr6:105047149
|
A | T | 1 | a0001c0001t0004g0004 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.383+20667A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047149 | ||||||
| chr6:105047194
|
A | C | 12 | a0001c0001t0004g0001a0001c0001t0004g0095a0001c0001t0004g0226others(9): Show | 13 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.383+20712A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047194 | ||||||
| chr6:105047230
|
G | A | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+20748G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047230 | ||||||
| chr6:105047230
|
G | C | 2 | a0001c0001t0014g0059a0001c0001t0014g0235 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383+20748G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047230 | ||||||
| chr6:105047307
|
T | C | 1 | a0001c0001t0004g0004 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.383+20825T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047307 | ||||||
| chr6:105047308
|
G | A | 1 | a0001c0001t0004g0004 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.383+20826G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047308 | ||||||
| chr6:105047375
|
G | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(184): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.383+20893G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047375 | ||||||
| chr6:105047380
|
C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.383+20898C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047380 | ||||||
| chr6:105047679
|
C | T | 1 | a0001c0001t0007g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.383+21197C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047679 | ||||||
| chr6:105047849
|
G | A | 3 | a0001c0001t0008g0132a0001c0001t0008g0147a0001c0001t0008g0157 | 3 | NA18948.hp2 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.383+21367G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047849 | ||||||
| chr6:105047926
|
G | T | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+21444G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047926 | ||||||
| chr6:105047930
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.383+21448T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047930 | ||||||
| chr6:105047948
|
A | G | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+21466A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105047948 | ||||||
| chr6:105048280
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(179): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.383+21798G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105048280 | ||||||
| chr6:105048328
|
T | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+21846T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105048328 | ||||||
| chr6:105048391
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.383+21909G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105048391 | ||||||
| chr6:105048492
|
T | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+22010T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105048492 | ||||||
| chr6:105048703
|
C | T | 1 | a0001c0001t0008g0132 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.383+22221C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105048703 | ||||||
| chr6:105048809
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.383+22327T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105048809 | ||||||
| chr6:105048852
|
T | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(185): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.383+22370T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105048852 | ||||||
| chr6:105048864
|
C | G | 1 | a0001c0001t0004g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.383+22382C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105048864 | ||||||
| chr6:105049110
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.383+22628G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049110 | ||||||
| chr6:105049143
|
C | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.383+22661C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049143 | ||||||
| chr6:105049143
|
C | T | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.383+22661C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049143 | ||||||
| chr6:105049433
|
A | G | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.383+22951A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049433 | ||||||
| chr6:105049470
|
G | T | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+22988G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049470 | ||||||
| chr6:105049486
|
G | T | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+23004G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049486 | ||||||
| chr6:105049520
|
G | A | 29 | a0001c0001t0002g0082a0001c0001t0002g0124a0001c0001t0002g0129others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.383+23038G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049520 | ||||||
| chr6:105049651
|
T | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.383+23169T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049651 | ||||||
| chr6:105049668
|
T | G | 11 | a0001c0001t0002g0182a0001c0001t0002g0199a0001c0001t0002g0200others(8): Show | 11 | NA18942.hp2 NA18947.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.383+23186T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049668 | ||||||
| chr6:105049775
|
A | G | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+23293A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049775 | ||||||
| chr6:105049815
|
G | A | 1 | a0001c0001t0004g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.383+23333G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049815 | ||||||
| chr6:105049885
|
CTA | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.383+23405_383+2340 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105049885 | |||||
| chr6:105049940
|
C | T | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+23458C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049940 | ||||||
| chr6:105049967
|
T | C | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+23485T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105049967 | ||||||
| chr6:105050028
|
T | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(186): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.383+23546T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050028 | ||||||
| chr6:105050059
|
T | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(181): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.383+23577T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050059 | ||||||
| chr6:105050069
|
G | A | 1 | a0001c0001t0007g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.383+23587G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050069 | ||||||
| chr6:105050192
|
G | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(170): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.383+23710G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050192 | ||||||
| chr6:105050258
|
T | C | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+23776T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050258 | ||||||
| chr6:105050303
|
T | A | 1 | a0001c0001t0003g0101 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.383+23821T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050303 | ||||||
| chr6:105050331
|
G | A | 1 | a0001c0001t0003g0268 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.383+23849G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050331 | ||||||
| chr6:105050368
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.383+23886C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050368 | ||||||
| chr6:105050458
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.383+23976C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050458 | ||||||
| chr6:105050474
|
T | C | 4 | a0001c0001t0004g0097a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+23992T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050474 | ||||||
| chr6:105050481
|
A | G | 4 | a0001c0001t0004g0097a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+23999A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050481 | ||||||
| chr6:105050519
|
G | A | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+24037G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050519 | ||||||
| chr6:105050526
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383+24044C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050526 | ||||||
| chr6:105050559
|
G | C | 1 | a0001c0001t0004g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.383+24077G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050559 | ||||||
| chr6:105050575
|
GTCCAGCC others(823): Show |
G | 3 | a0001c0001t0009g0017a0001c0001t0009g0061a0001c0001t0009g0227 | 3 | HG02615.hp2 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.383+24126_383+2495 others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050575 | |||||
| chr6:105050596
|
G | A | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.383+24114G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050596 | ||||||
| chr6:105050604
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.383+24122G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050604 | ||||||
| chr6:105050608
|
C | CA | 59 | a0001c0001t0002g0007a0001c0001t0002g0016a0001c0001t0002g0020others(56): Show | 59 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.383+24152dupA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
C | CAA | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(15): Show | 18 | HG01255.hp1 HG01517.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.383+24151_383+2415 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
C | CAAA | 74 | a0001c0001t0002g0124a0001c0001t0003g0065a0001c0001t0003g0066others(71): Show | 75 | HG00423.hp2 HG01069.hp1 HG01167.hp1 others(72): Show |
intron_variant | MODIFIER | c.383+24150_383+2415 others(7): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
C | CAAAA | 31 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(28): Show | 31 | HG00735.hp1 HG01106.hp2 HG01981.hp2 others(28): Show |
intron_variant | MODIFIER | c.383+24149_383+2415 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
C | CAAAAA | 40 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(37): Show | 40 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.383+24148_383+2415 others(9): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
C | CAAAAAA | 22 | a0001c0001t0001g0026a0001c0001t0001g0091a0001c0001t0001g0134others(19): Show | 22 | HG00140.hp1 HG00642.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.383+24147_383+2415 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
C | CAAAAAAA | 8 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0130others(5): Show | 8 | HG00099.hp2 HG01255.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.383+24146_383+2415 others(11): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0144 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.383+24141_383+2415 others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
CAAAAAAA others(3): Show |
C | 10 | a0001c0001t0001g0118a0001c0001t0001g0125a0001c0001t0001g0137others(7): Show | 10 | HG00558.hp1 HG02027.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.383+24143_383+2415 others(14): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050608
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0002g0122a0001c0001t0002g0239 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.383+24141_383+2415 others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105050608 | |||||
| chr6:105050782
|
A | G | 1 | a0001c0001t0003g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.383+24300A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105050782 | ||||||
| chr6:105051206
|
C | A | 1 | a0001c0001t0019g0202 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.383+24724C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051206 | ||||||
| chr6:105051209
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.383+24727G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051209 | ||||||
| chr6:105051307
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(170): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.383+24825C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051307 | ||||||
| chr6:105051356
|
T | C | 1 | a0001c0001t0003g0148 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.383+24874T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051356 | ||||||
| chr6:105051422
|
G | A | 1 | a0001c0001t0014g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.383+24940G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051422 | ||||||
| chr6:105051434
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(1): Show | 4 | HG00735.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+24952G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051434 | ||||||
| chr6:105051658
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.383+25176A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051658 | ||||||
| chr6:105051734
|
C | CA | 204 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.383+25252_383+2525 others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051734 | ||||||
| chr6:105051837
|
T | C | 4 | a0001c0001t0004g0097a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+25355T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051837 | ||||||
| chr6:105051843
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.383+25361C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105051843 | ||||||
| chr6:105052049
|
G | A | 1 | a0001c0001t0003g0073 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.383+25567G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105052049 | ||||||
| chr6:105052141
|
C | A | 1 | a0001c0001t0011g0076 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.383+25659C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105052141 | ||||||
| chr6:105052215
|
G | A | 1 | a0001c0001t0002g0242 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.383+25733G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105052215 | ||||||
| chr6:105052258
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383+25776T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105052258 | ||||||
| chr6:105052321
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.383+25839C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105052321 | ||||||
| chr6:105052557
|
C | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-25857C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105052557 | ||||||
| chr6:105052877
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.384-25537C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105052877 | ||||||
| chr6:105052888
|
G | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(179): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.384-25526G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105052888 | ||||||
| chr6:105053049
|
A | G | 1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-25365A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053049 | ||||||
| chr6:105053310
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.384-25104T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053310 | ||||||
| chr6:105053382
|
G | GGT | 18 | a0001c0001t0002g0229a0001c0001t0003g0087a0001c0001t0004g0060others(15): Show | 18 | HG02109.hp1 HG02647.hp1 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.384-25002_384-2500 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053382 | |||||
| chr6:105053382
|
G | GGTGT | 86 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.384-25004_384-2500 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053382 | |||||
| chr6:105053382
|
G | GGTGTGT | 22 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0111others(19): Show | 22 | HG01243.hp1 HG01433.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.384-25006_384-2500 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053382 | |||||
| chr6:105053382
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0014g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.384-25010_384-2500 others(14): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053382 | |||||
| chr6:105053382
|
GGT | G | 3 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0033 | 3 | HG02723.hp2 NA18942.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.384-25002_384-2500 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053382 | |||||
| chr6:105053382
|
GGTGTGT | G | 40 | a0001c0001t0002g0016a0001c0001t0002g0021a0001c0001t0002g0062others(37): Show | 40 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.384-25006_384-2500 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053382 | |||||
| chr6:105053546
|
G | A | 1 | a0001c0001t0003g0224 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.384-24868G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053546 | ||||||
| chr6:105053714
|
C | CATGTGT | 3 | a0001c0001t0001g0018a0001c0001t0001g0276a0001c0001t0004g0187 | 3 | HG01891.hp2 HG01943.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.384-24700_384-2469 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CATGTGTG others(1): Show |
14 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0125others(11): Show | 14 | HG01243.hp1 HG02027.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.384-24700_384-2469 others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CATGTGTG others(3): Show |
63 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0026others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.384-24700_384-2469 others(14): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CATGTGTG others(5): Show |
14 | a0001c0001t0001g0027a0001c0001t0001g0051a0001c0001t0001g0111others(11): Show | 14 | HG00323.hp1 HG00558.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.384-24700_384-2469 others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CATGTGTG others(7): Show |
2 | a0001c0001t0001g0137a0001c0001t0025g0112 | 2 | HG02132.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.384-24700_384-2469 others(18): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CATGTGTG others(9): Show |
2 | a0001c0001t0006g0169a0001c0001t0006g0171 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.384-24700_384-2469 others(20): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CATGTGTG others(11): Show |
2 | a0001c0001t0006g0172a0001c0002t0007g0005 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.384-24700_384-2469 others(22): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CATGTGTG others(13): Show |
5 | a0001c0001t0004g0153a0001c0001t0006g0154a0001c0001t0006g0173others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-24700_384-2469 others(24): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CATTGTGT others(4): Show |
1 | a0001c0001t0001g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.384-24700_384-2469 others(15): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053714 | ||||||
| chr6:105053714
|
C | CGT | 56 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(53): Show | 56 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.384-24671_384-2467 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053714 | |||||
| chr6:105053714
|
C | CGTGT | 8 | a0001c0001t0002g0020a0001c0001t0002g0031a0001c0001t0005g0036others(5): Show | 8 | HG01243.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.384-24673_384-2467 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053714 | |||||
| chr6:105053714
|
C | CGTGTGT | 6 | a0001c0001t0001g0167a0001c0001t0004g0003a0001c0001t0004g0053others(3): Show | 6 | HG02717.hp2 HG03041.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.384-24675_384-2467 others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053714 | |||||
| chr6:105053714
|
C | CGTGTGTG others(1): Show |
15 | a0001c0001t0004g0001a0001c0001t0004g0095a0001c0001t0004g0226others(12): Show | 16 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.384-24677_384-2467 others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053714 | |||||
| chr6:105053714
|
C | CGTGTGTG others(3): Show |
7 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0052others(4): Show | 7 | HG01891.hp1 HG02896.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-24679_384-2467 others(14): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053714 | |||||
| chr6:105053714
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0005g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384-24681_384-2467 others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053714 | |||||
| chr6:105053714
|
CGT | C | 47 | a0001c0001t0001g0258a0001c0001t0002g0007a0001c0001t0002g0252others(44): Show | 47 | HG01106.hp2 HG01167.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.384-24671_384-2467 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053714 | |||||
| chr6:105053714
|
CGTGT | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-24673_384-2467 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105053714 | |||||
| chr6:105053715
|
G | A | 17 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0074others(14): Show | 17 | HG00423.hp2 HG01928.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.384-24699G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053715 | ||||||
| chr6:105053717
|
G | A | 42 | a0001c0001t0001g0258a0001c0001t0003g0067a0001c0001t0003g0068others(39): Show | 42 | HG01106.hp2 HG01167.hp2 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.384-24697G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053717 | ||||||
| chr6:105053719
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-24695G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053719 | ||||||
| chr6:105053900
|
C | T | 1 | a0001c0001t0004g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.384-24514C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053900 | ||||||
| chr6:105053925
|
G | A | 16 | a0001c0001t0001g0167a0001c0001t0004g0001a0001c0001t0004g0028others(13): Show | 17 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.384-24489G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053925 | ||||||
| chr6:105053978
|
A | T | 2 | a0001c0001t0004g0060a0001c0001t0025g0112 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.384-24436A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105053978 | ||||||
| chr6:105054004
|
A | G | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.384-24410A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054004 | ||||||
| chr6:105054005
|
A | G | 4 | a0001c0001t0001g0115a0001c0001t0001g0168a0001c0001t0001g0216others(1): Show | 4 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-24409A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054005 | ||||||
| chr6:105054041
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.384-24373G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054041 | ||||||
| chr6:105054046
|
CTGTT | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(179): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.384-24358_384-2435 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105054046 | |||||
| chr6:105054674
|
A | G | 19 | a0001c0001t0001g0167a0001c0001t0004g0001a0001c0001t0004g0003others(16): Show | 20 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.384-23740A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054674 | ||||||
| chr6:105054781
|
C | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(179): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.384-23633C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054781 | ||||||
| chr6:105054794
|
G | T | 2 | a0001c0001t0001g0151a0001c0001t0003g0149 | 2 | NA18940.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.384-23620G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054794 | ||||||
| chr6:105054812
|
C | T | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.384-23602C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054812 | ||||||
| chr6:105054815
|
T | C | 1 | a0001c0001t0004g0004 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.384-23599T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054815 | ||||||
| chr6:105054845
|
C | CT | 53 | a0001c0001t0001g0276a0001c0001t0002g0016a0001c0001t0002g0021others(50): Show | 53 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.384-23551dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105054845 | |||||
| chr6:105054845
|
CT | C | 23 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(20): Show | 23 | HG00735.hp1 HG01243.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.384-23551delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105054845 | |||||
| chr6:105054916
|
C | T | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-23498C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054916 | ||||||
| chr6:105054930
|
G | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-23484G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105054930 | ||||||
| chr6:105055106
|
G | T | 5 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0052others(2): Show | 5 | HG01891.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-23308G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105055106 | ||||||
| chr6:105055332
|
A | G | 1 | a0001c0001t0011g0076 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.384-23082A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105055332 | ||||||
| chr6:105055387
|
T | C | 1 | a0001c0001t0003g0184 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.384-23027T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105055387 | ||||||
| chr6:105055645
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.384-22769C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105055645 | ||||||
| chr6:105055919
|
C | CT | 167 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(164): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.384-22474dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105055919 | |||||
| chr6:105055919
|
C | CTT | 28 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0117others(25): Show | 28 | HG00558.hp1 HG01433.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.384-22475_384-2247 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105055919 | |||||
| chr6:105055990
|
G | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(181): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.384-22424G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105055990 | ||||||
| chr6:105056039
|
G | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-22375G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105056039 | ||||||
| chr6:105056204
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.384-22210G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105056204 | ||||||
| chr6:105056261
|
A | ATTTT | 149 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(146): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.384-22149_384-2214 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105056261 | |||||
| chr6:105056301
|
A | G | 13 | a0001c0001t0001g0167a0001c0001t0004g0001a0001c0001t0004g0095others(10): Show | 14 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.384-22113A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105056301 | ||||||
| chr6:105056691
|
C | T | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.384-21723C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105056691 | ||||||
| chr6:105056741
|
A | G | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-21673A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105056741 | ||||||
| chr6:105057000
|
T | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(1): Show | 4 | HG00735.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-21414T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057000 | ||||||
| chr6:105057060
|
C | A | 2 | a0001c0001t0003g0066a0001c0001t0003g0208 | 2 | HG01928.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.384-21354C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057060 | ||||||
| chr6:105057064
|
T | C | 8 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0103others(5): Show | 8 | NA18939.hp2 NA18947.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.384-21350T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057064 | ||||||
| chr6:105057113
|
C | T | 2 | a0001c0001t0004g0060a0001c0001t0025g0112 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.384-21301C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057113 | ||||||
| chr6:105057304
|
T | A | 1 | a0001c0001t0003g0093 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.384-21110T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057304 | ||||||
| chr6:105057375
|
G | T | 3 | a0001c0001t0009g0017a0001c0001t0009g0061a0001c0001t0009g0227 | 3 | HG02615.hp2 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.384-21039G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057375 | ||||||
| chr6:105057703
|
T | C | 1 | a0001c0001t0003g0269 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.384-20711T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057703 | ||||||
| chr6:105057730
|
T | G | 1 | a0001c0001t0004g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.384-20684T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057730 | ||||||
| chr6:105057744
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.384-20670A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057744 | ||||||
| chr6:105057954
|
G | A | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-20460G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057954 | ||||||
| chr6:105057976
|
C | G | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.384-20438C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105057976 | ||||||
| chr6:105058091
|
T | C | 1 | a0001c0001t0003g0072 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.384-20323T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058091 | ||||||
| chr6:105058094
|
C | T | 17 | a0001c0001t0001g0167a0001c0001t0004g0001a0001c0001t0004g0028others(14): Show | 18 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.384-20320C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058094 | ||||||
| chr6:105058244
|
C | T | 1 | a0001c0001t0009g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.384-20170C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058244 | ||||||
| chr6:105058277
|
C | T | 5 | a0001c0001t0001g0258a0001c0001t0003g0264a0001c0001t0003g0265others(2): Show | 5 | HG02135.hp2 NA18940.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-20137C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058277 | ||||||
| chr6:105058304
|
T | C | 3 | a0001c0001t0009g0017a0001c0001t0009g0061a0001c0001t0009g0227 | 3 | HG02615.hp2 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.384-20110T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058304 | ||||||
| chr6:105058345
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0042others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-20069T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058345 | ||||||
| chr6:105058367
|
G | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(202): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.384-20047G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058367 | ||||||
| chr6:105058401
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0216 | 2 | HG01069.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.384-20013G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058401 | ||||||
| chr6:105058466
|
A | G | 1 | a0001c0001t0023g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.384-19948A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058466 | ||||||
| chr6:105058611
|
T | A | 1 | a0001c0001t0003g0080 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.384-19803T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105058611 | ||||||
| chr6:105059004
|
C | T | 2 | a0001c0001t0013g0056a0001c0001t0013g0058 | 2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.384-19410C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059004 | ||||||
| chr6:105059036
|
G | A | 2 | a0001c0001t0005g0040a0001c0001t0005g0043 | 2 | HG01243.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.384-19378G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059036 | ||||||
| chr6:105059036
|
G | C | 59 | a0001c0001t0001g0151a0001c0001t0001g0258a0001c0001t0003g0065others(56): Show | 59 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.384-19378G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059036 | ||||||
| chr6:105059037
|
C | T | 59 | a0001c0001t0001g0151a0001c0001t0001g0258a0001c0001t0003g0065others(56): Show | 59 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.384-19377C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059037 | ||||||
| chr6:105059139
|
T | C | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.384-19275T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059139 | ||||||
| chr6:105059219
|
AT | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(171): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.384-19184delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105059219 | |||||
| chr6:105059262
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.384-19152T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059262 | ||||||
| chr6:105059291
|
A | G | 1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-19123A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059291 | ||||||
| chr6:105059481
|
G | T | 1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-18933G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059481 | ||||||
| chr6:105059725
|
A | G | 1 | a0001c0001t0003g0087 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.384-18689A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059725 | ||||||
| chr6:105059741
|
A | G | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-18673A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059741 | ||||||
| chr6:105059840
|
T | A | 5 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-18574T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059840 | ||||||
| chr6:105059841
|
T | G | 1 | a0001c0001t0003g0203 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.384-18573T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059841 | ||||||
| chr6:105059907
|
AT | A | 15 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0042others(12): Show | 15 | HG00423.hp1 HG00558.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.384-18494delT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105059907 | |||||
| chr6:105059907
|
ATT | A | 57 | a0001c0001t0001g0191a0001c0001t0001g0258a0001c0001t0003g0065others(54): Show | 57 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.384-18495_384-1849 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105059907 | |||||
| chr6:105059945
|
C | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-18469C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059945 | ||||||
| chr6:105059989
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.384-18425C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105059989 | ||||||
| chr6:105060524
|
T | G | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.384-17890T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105060524 | ||||||
| chr6:105060997
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.384-17417A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105060997 | ||||||
| chr6:105061047
|
A | T | 3 | a0001c0001t0004g0004a0001c0001t0004g0060a0001c0001t0025g0112 | 3 | HG02145.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.384-17367A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105061047 | ||||||
| chr6:105061113
|
G | T | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.384-17301G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105061113 | ||||||
| chr6:105061167
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0111a0001c0001t0001g0241 | 3 | HG02451.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.384-17247T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105061167 | ||||||
| chr6:105061342
|
G | A | 15 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0125others(12): Show | 15 | HG00558.hp1 HG02027.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.384-17072G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105061342 | ||||||
| chr6:105061557
|
A | G | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.384-16857A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105061557 | ||||||
| chr6:105061610
|
G | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.384-16804G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105061610 | ||||||
| chr6:105061617
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.384-16797A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105061617 | ||||||
| chr6:105061712
|
T | C | 1 | a0001c0001t0014g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.384-16702T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105061712 | ||||||
| chr6:105062061
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.384-16353C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105062061 | ||||||
| chr6:105062276
|
G | A | 1 | a0001c0001t0009g0017 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.384-16138G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105062276 | ||||||
| chr6:105062557
|
ACT | A | 14 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(11): Show | 14 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.384-15855_384-1585 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105062557 | |||||
| chr6:105063519
|
C | T | 1 | a0001c0001t0024g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.384-14895C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063519 | ||||||
| chr6:105063635
|
CG | C | 70 | a0001c0001t0001g0183a0001c0001t0002g0009a0001c0001t0002g0010others(67): Show | 70 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.384-14766delG | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105063635 | |||||
| chr6:105063641
|
G | T | 14 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(11): Show | 14 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.384-14773G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063641 | ||||||
| chr6:105063644
|
G | T | 16 | a0001c0001t0004g0001a0001c0001t0004g0028a0001c0001t0004g0029others(13): Show | 17 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.384-14770G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063644 | ||||||
| chr6:105063646
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(77): Show | 80 | HG00140.hp1 HG00558.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.384-14768G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063646 | ||||||
| chr6:105063647
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.384-14767G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063647 | ||||||
| chr6:105063647
|
G | GA | 8 | a0001c0001t0001g0151a0001c0001t0003g0073a0001c0001t0003g0077others(5): Show | 8 | HG01167.hp2 HG03540.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.384-14767_384-1476 others(5): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063647 | ||||||
| chr6:105063648
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.384-14766G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063648 | ||||||
| chr6:105063649
|
A | G | 25 | a0001c0001t0002g0032a0001c0001t0002g0110a0001c0001t0002g0166others(22): Show | 26 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.384-14765A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063649 | ||||||
| chr6:105063650
|
A | G | 3 | a0001c0001t0002g0166a0001c0001t0004g0003a0001c0001t0004g0053 | 3 | HG03041.hp2 NA18954.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.384-14764A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063650 | ||||||
| chr6:105063801
|
C | A | 1 | a0001c0001t0003g0096 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.384-14613C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063801 | ||||||
| chr6:105063844
|
A | AT | 9 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0164others(6): Show | 9 | HG00323.hp1 HG02109.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.384-14559dupT | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105063844 | |||||
| chr6:105063844
|
A | ATT | 179 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(176): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.384-14560_384-1455 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105063844 | |||||
| chr6:105063906
|
T | A | 3 | a0001c0001t0009g0017a0001c0001t0009g0061a0001c0001t0009g0227 | 3 | HG02615.hp2 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.384-14508T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105063906 | ||||||
| chr6:105064009
|
AAG | A | 3 | a0001c0001t0004g0004a0001c0001t0004g0060a0001c0001t0025g0112 | 3 | HG02145.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.384-14403_384-1440 others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105064009 | |||||
| chr6:105064187
|
T | G | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-14227T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105064187 | ||||||
| chr6:105064257
|
G | T | 5 | a0001c0001t0003g0086a0001c0001t0003g0100a0001c0001t0003g0150others(2): Show | 5 | HG02027.hp1 NA18962.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-14157G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105064257 | ||||||
| chr6:105064304
|
A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(185): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.384-14110A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105064304 | ||||||
| chr6:105064717
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0042others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-13697C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105064717 | ||||||
| chr6:105064747
|
A | G | 1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-13667A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105064747 | ||||||
| chr6:105065010
|
G | A | 1 | a0001c0001t0014g0059 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.384-13404G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105065010 | ||||||
| chr6:105065236
|
T | A | 1 | a0002c0003t0002g0237 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.384-13178T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105065236 | ||||||
| chr6:105065363
|
A | G | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-13051A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105065363 | ||||||
| chr6:105065496
|
G | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(202): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.384-12918G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105065496 | ||||||
| chr6:105065541
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.384-12873A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105065541 | ||||||
| chr6:105065695
|
T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.384-12719T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105065695 | ||||||
| chr6:105065845
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.384-12569G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105065845 | ||||||
| chr6:105065931
|
C | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0111a0001c0001t0001g0241 | 3 | HG02451.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.384-12483C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105065931 | ||||||
| chr6:105066001
|
G | A | 1 | a0001c0001t0003g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.384-12413G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105066001 | ||||||
| chr6:105066200
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.384-12214G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105066200 | ||||||
| chr6:105066259
|
A | G | 1 | a0001c0001t0007g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.384-12155A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105066259 | ||||||
| chr6:105066285
|
T | G | 3 | a0001c0001t0009g0017a0001c0001t0009g0061a0001c0001t0009g0227 | 3 | HG02615.hp2 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.384-12129T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105066285 | ||||||
| chr6:105066417
|
C | T | 2 | a0001c0001t0003g0088a0001c0001t0003g0096 | 2 | NA19011.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.384-11997C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105066417 | ||||||
| chr6:105066518
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.384-11896G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105066518 | ||||||
| chr6:105066613
|
T | C | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-11801T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105066613 | ||||||
| chr6:105066703
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.384-11711A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105066703 | ||||||
| chr6:105067089
|
G | T | 1 | a0001c0001t0003g0094 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.384-11325G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105067089 | ||||||
| chr6:105067242
|
T | C | 3 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0208 | 3 | HG01928.hp1 HG01928.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.384-11172T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105067242 | ||||||
| chr6:105067621
|
GTTGT | G | 17 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0028others(14): Show | 18 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.384-10790_384-1078 others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105067621 | |||||
| chr6:105067708
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.384-10706C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105067708 | ||||||
| chr6:105067948
|
A | G | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-10466A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105067948 | ||||||
| chr6:105068028
|
G | T | 1 | a0001c0001t0009g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.384-10386G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105068028 | ||||||
| chr6:105068030
|
T | A | 5 | a0001c0001t0002g0021a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-10384T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105068030 | ||||||
| chr6:105068031
|
G | T | 5 | a0001c0001t0002g0021a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-10383G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105068031 | ||||||
| chr6:105068364
|
C | A | 1 | a0001c0001t0004g0004 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.384-10050C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105068364 | ||||||
| chr6:105068448
|
T | A | 6 | a0001c0001t0001g0138a0001c0001t0004g0095a0001c0001t0004g0244others(3): Show | 6 | HG01516.hp2 HG01517.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.384-9966T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105068448 | ||||||
| chr6:105068578
|
C | T | 19 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0028others(16): Show | 20 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.384-9836C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105068578 | ||||||
| chr6:105068597
|
A | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG00558.hp1 HG02083.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-9817A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105068597 | ||||||
| chr6:105069287
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0111a0001c0001t0001g0241 | 3 | HG02451.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.384-9127C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105069287 | ||||||
| chr6:105069409
|
G | A | 1 | a0001c0001t0004g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.384-9005G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105069409 | ||||||
| chr6:105069463
|
GC | G | 5 | a0001c0001t0002g0021a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-8949delC | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105069463 | |||||
| chr6:105069554
|
G | A | 1 | a0001c0001t0003g0100 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.384-8860G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105069554 | ||||||
| chr6:105069569
|
T | TA | 21 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0028others(18): Show | 22 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.384-8845_384-8844i others(3): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105069569 | ||||||
| chr6:105069570
|
T | A | 248 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.384-8844T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105069570 | ||||||
| chr6:105069688
|
CA | C | 8 | a0001c0001t0001g0125a0001c0001t0001g0139a0001c0001t0001g0167others(5): Show | 8 | HG01516.hp1 HG02027.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.384-8712delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105069688 | |||||
| chr6:105069993
|
T | A | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.384-8421T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105069993 | ||||||
| chr6:105070105
|
G | A | 13 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0024others(10): Show | 13 | HG00642.hp1 HG02723.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.384-8309G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070105 | ||||||
| chr6:105070255
|
T | C | 1 | a0001c0001t0014g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-8159T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070255 | ||||||
| chr6:105070405
|
C | A | 2 | a0001c0001t0004g0003a0001c0001t0004g0053 | 2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.384-8009C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070405 | ||||||
| chr6:105070478
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-7936G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070478 | ||||||
| chr6:105070588
|
A | C | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.384-7826A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070588 | ||||||
| chr6:105070590
|
A | C | 1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.384-7824A>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070590 | ||||||
| chr6:105070592
|
C | CACACACA others(4): Show |
1 | a0001c0001t0017g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.384-7822_384-7821i others(13): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070592 | ||||||
| chr6:105070592
|
C | CACACACA others(12): Show |
1 | a0001c0001t0004g0240 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.384-7822_384-7821i others(21): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070592 | ||||||
| chr6:105070592
|
C | CACACACA others(14): Show |
2 | a0001c0001t0001g0131a0001c0001t0007g0048 | 2 | HG03225.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.384-7822_384-7821i others(23): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070592 | ||||||
| chr6:105070592
|
C | CCA | 36 | a0001c0001t0001g0091a0001c0001t0002g0007a0001c0001t0002g0016others(33): Show | 36 | HG00423.hp1 HG00558.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.384-7774_384-7773d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACA | 18 | a0001c0001t0001g0133a0001c0001t0001g0138a0001c0001t0001g0276others(15): Show | 18 | HG01069.hp1 HG01978.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.384-7776_384-7773d others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACA | 14 | a0001c0001t0001g0111a0001c0001t0001g0139a0001c0001t0001g0152others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.384-7778_384-7773d others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(1): Show |
11 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0125others(8): Show | 11 | HG02027.hp2 HG02970.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.384-7780_384-7773d others(10): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(3): Show |
20 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(17): Show | 20 | HG00558.hp1 HG00735.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.384-7782_384-7773d others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(5): Show |
16 | a0001c0001t0001g0002a0001c0001t0001g0181a0001c0001t0001g0207others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.384-7784_384-7773d others(14): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(7): Show |
22 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0130others(19): Show | 22 | HG00099.hp2 HG01074.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.384-7786_384-7773d others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(9): Show |
18 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0115others(15): Show | 19 | HG00140.hp2 HG00323.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.384-7788_384-7773d others(18): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(11): Show |
15 | a0001c0001t0001g0026a0001c0001t0001g0098a0001c0001t0001g0140others(12): Show | 15 | HG01167.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.384-7790_384-7773d others(20): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(13): Show |
3 | a0001c0001t0001g0194a0001c0001t0004g0226a0001c0001t0006g0169 | 3 | HG02683.hp1 HG03516.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.384-7792_384-7773d others(22): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(15): Show |
5 | a0001c0001t0001g0015a0001c0001t0001g0232a0001c0001t0004g0254others(2): Show | 5 | HG01358.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-7794_384-7773d others(24): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(17): Show |
3 | a0001c0001t0001g0144a0001c0001t0001g0192a0001c0001t0001g0223 | 3 | HG00642.hp2 HG02698.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.384-7796_384-7773d others(26): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
C | CCACACAC others(21): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0216a0001c0002t0007g0005 | 3 | HG01069.hp2 HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.384-7800_384-7773d others(30): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
CCA | C | 42 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0033others(39): Show | 42 | HG00423.hp2 HG01167.hp2 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.384-7774_384-7773d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
CCACA | C | 4 | a0001c0001t0002g0236a0001c0001t0003g0090a0001c0001t0003g0267others(1): Show | 4 | HG01515.hp2 HG02145.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-7776_384-7773d others(6): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
CCACACA | C | 8 | a0001c0001t0003g0070a0001c0001t0003g0073a0001c0001t0003g0099others(5): Show | 8 | HG01516.hp1 HG02135.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.384-7778_384-7773d others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
CCACACAC others(3): Show |
C | 1 | a0001c0001t0003g0148 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.384-7782_384-7773d others(12): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
CCACACAC others(7): Show |
C | 4 | a0001c0001t0001g0055a0001c0001t0003g0088a0001c0001t0003g0096others(1): Show | 4 | HG03041.hp1 HG06807.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-7786_384-7773d others(16): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070592
|
CCACACAC others(13): Show |
C | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.384-7792_384-7773d others(22): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105070592 | |||||
| chr6:105070756
|
C | G | 1 | a0001c0001t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.384-7658C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070756 | ||||||
| chr6:105070824
|
A | G | 1 | a0001c0001t0007g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.384-7590A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070824 | ||||||
| chr6:105070899
|
C | T | 2 | a0001c0001t0004g0060a0001c0001t0025g0112 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.384-7515C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105070899 | ||||||
| chr6:105071080
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.384-7334T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105071080 | ||||||
| chr6:105071319
|
G | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(203): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.384-7095G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105071319 | ||||||
| chr6:105071374
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.384-7040A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105071374 | ||||||
| chr6:105071377
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(180): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.384-7037A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105071377 | ||||||
| chr6:105071593
|
G | C | 1 | a0001c0001t0018g0190 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.384-6821G>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105071593 | ||||||
| chr6:105071799
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.384-6615T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105071799 | ||||||
| chr6:105072088
|
C | CTG | 34 | a0001c0001t0002g0082a0001c0001t0002g0124a0001c0001t0002g0129others(31): Show | 34 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.384-6306_384-6305d others(4): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105072088 | |||||
| chr6:105072088
|
C | CTGTGTG | 5 | a0001c0001t0004g0003a0001c0001t0004g0053a0001c0001t0007g0006others(2): Show | 5 | HG02109.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-6310_384-6305d others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105072088 | |||||
| chr6:105072088
|
C | G | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-6326C>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105072088 | ||||||
| chr6:105072154
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.384-6260A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105072154 | ||||||
| chr6:105072427
|
TTAAAAG | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | NA18950.hp1 NA18965.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-5978_384-5973d others(8): Show |
LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105072427 | |||||
| chr6:105072639
|
G | A | 12 | a0001c0001t0005g0008a0001c0001t0005g0019a0001c0001t0005g0034others(9): Show | 12 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.384-5775G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105072639 | ||||||
| chr6:105072755
|
G | A | 59 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(56): Show | 59 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.384-5659G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105072755 | ||||||
| chr6:105072954
|
G | A | 5 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0013others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-5460G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105072954 | ||||||
| chr6:105073452
|
G | A | 7 | a0001c0001t0002g0182a0001c0001t0002g0259a0001c0001t0002g0260others(4): Show | 7 | NA18942.hp2 NA18948.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-4962G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105073452 | ||||||
| chr6:105073472
|
G | A | 2 | a0001c0001t0006g0173a0001c0001t0006g0174 | 2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.384-4942G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105073472 | ||||||
| chr6:105074236
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.384-4178C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105074236 | ||||||
| chr6:105074284
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0048a0001c0001t0007g0057others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-4130G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105074284 | ||||||
| chr6:105074322
|
C | T | 1 | a0001c0002t0007g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.384-4092C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105074322 | ||||||
| chr6:105074333
|
G | T | 2 | a0001c0001t0014g0059a0001c0001t0014g0235 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.384-4081G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105074333 | ||||||
| chr6:105074449
|
C | T | 7 | a0001c0001t0006g0154a0001c0001t0006g0169a0001c0001t0006g0171others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-3965C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105074449 | ||||||
| chr6:105075313
|
C | A | 2 | a0001c0001t0007g0006a0001c0001t0007g0057 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.384-3101C>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105075313 | ||||||
| chr6:105075434
|
T | C | 6 | a0001c0001t0003g0069a0001c0001t0003g0092a0001c0001t0003g0094others(3): Show | 6 | HG01516.hp1 HG02698.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-2980T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105075434 | ||||||
| chr6:105075804
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(179): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.384-2610C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105075804 | ||||||
| chr6:105076012
|
A | G | 1 | a0001c0001t0002g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.384-2402A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105076012 | ||||||
| chr6:105076053
|
A | G | 1 | a0001c0001t0003g0073 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.384-2361A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105076053 | ||||||
| chr6:105076412
|
A | G | 5 | a0001c0001t0003g0149a0001c0001t0003g0264a0001c0001t0003g0265others(2): Show | 5 | HG02135.hp2 NA18940.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-2002A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105076412 | ||||||
| chr6:105076418
|
G | T | 1 | a0001c0001t0004g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.384-1996G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105076418 | ||||||
| chr6:105076614
|
G | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.384-1800G>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105076614 | ||||||
| chr6:105076627
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.384-1787G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105076627 | ||||||
| chr6:105076843
|
A | G | 1 | a0001c0001t0023g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.384-1571A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105076843 | ||||||
| chr6:105076846
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.384-1568C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105076846 | ||||||
| chr6:105077157
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.384-1257G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077157 | ||||||
| chr6:105077229
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.384-1185A>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077229 | ||||||
| chr6:105077231
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.384-1183T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077231 | ||||||
| chr6:105077246
|
T | C | 3 | a0001c0001t0004g0004a0001c0001t0004g0060a0001c0001t0025g0112 | 3 | HG02145.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.384-1168T>C | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077246 | ||||||
| chr6:105077363
|
T | A | 2 | a0001c0001t0004g0060a0001c0001t0025g0112 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.384-1051T>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077363 | ||||||
| chr6:105077416
|
A | G | 3 | a0001c0001t0004g0004a0001c0001t0004g0060a0001c0001t0025g0112 | 3 | HG02145.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.384-998A>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077416 | ||||||
| chr6:105077457
|
GA | G | 59 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(56): Show | 59 | HG00423.hp2 HG01106.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.384-953delA | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr6 | 105077457 | |||||
| chr6:105077686
|
C | T | 4 | a0001c0001t0004g0097a0001c0001t0004g0113a0001c0001t0004g0114others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-728C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077686 | ||||||
| chr6:105077693
|
C | T | 1 | a0001c0001t0004g0012 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.384-721C>T | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077693 | ||||||
| chr6:105077890
|
T | G | 2 | a0001c0001t0014g0059a0001c0001t0014g0235 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.384-524T>G | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105077890 | ||||||
| chr6:105078085
|
G | A | 2 | a0001c0001t0004g0003a0001c0001t0004g0053 | 2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.384-329G>A | LIN28B | ENSG00000187772.8 | transcript | ENST00000345080.5 | protein_coding | 3/3 | chr6 | 105078085 |