| geneid | 54790 |
|---|---|
| ensemblid | ENSG00000168769.14 |
| hgncid | 25941 |
| symbol | TET2 |
| name | tet methylcytosine dioxygenase 2 |
| refseq_nuc | NM_001127208.3 |
| refseq_prot | NP_001120680.1 |
| ensembl_nuc | ENST00000380013.9 |
| ensembl_prot | ENSP00000369351.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 105146876 |
| end | 105279803 |
| strand | + |
| ver | v1.2 |
| region | chr4:105146876-105279803 |
| region5000 | chr4:105141876-105284803 |
| regionname0 | TET2_chr4_105146876_105279803 |
| regionname5000 | TET2_chr4_105141876_105284803 |
| 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 | 1/0 | 2002 | 133 | 23 | 33 | 51 | 9 | 16 | 39 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002 | 0/0 | 2002 | 60 | 2 | 10 | 32 | 4 | 12 | 26 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003 | 0/0 | 2002 | 45 | 26 | 4 | 14 | 0 | 1 | 13 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004 | 0/0 | 2002 | 45 | 0 | 5 | 38 | 1 | 1 | 31 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0005 | 0/1 | 2002 | 20 | 7 | 7 | 3 | 0 | 2 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006 | 0/0 | 2002 | 17 | 16 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0007 | 0/0 | 2002 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0008 | 0/0 | 2002 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0009 | 0/0 | 2002 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0010 | 0/0 | 2002 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0011 | 0/0 | 2002 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0012 | 0/0 | 2002 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0013 | 0/0 | 2002 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0014 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0015 | 0/0 | 1459 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0016 | 0/0 | 2002 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0017 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0018 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0019 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0020 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0021 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| 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 | 1/0 | 6009 | 123 | 16 | 31 | 50 | 9 | 16 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0002 | 0/0 | 6009 | 59 | 2 | 10 | 31 | 4 | 12 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0003 | 0/0 | 6009 | 44 | 0 | 5 | 37 | 1 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0004 | 0/0 | 6009 | 33 | 16 | 3 | 14 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0005 | 0/1 | 6009 | 20 | 7 | 7 | 3 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0006 | 0/0 | 6009 | 17 | 16 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0007 | 0/0 | 6009 | 7 | 6 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0008 | 0/0 | 6009 | 6 | 5 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0009 | 0/0 | 6009 | 4 | 1 | 1 | 0 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0010 | 0/0 | 6009 | 4 | 4 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0011 | 0/0 | 6009 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0012 | 0/0 | 6009 | 3 | 0 | 0 | 3 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0013 | 0/0 | 6009 | 3 | 0 | 0 | 2 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0014 | 0/0 | 6009 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0015 | 0/0 | 6009 | 2 | 0 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0016 | 0/0 | 6009 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0017 | 0/0 | 6009 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0018 | 0/0 | 6009 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0019 | 0/0 | 6009 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0020 | 0/0 | 5959 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0021 | 0/0 | 6009 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0022 | 0/0 | 6009 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0023 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0024 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0025 | 0/0 | 6009 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0026 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0027 | 0/0 | 6009 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0028 | 0/0 | 6009 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0029 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0030 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0031 | 0/0 | 6009 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| c0032 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3581 | 45 | 2 | 4 | 27 | 2 | 9 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0002 | 0/0 | 3578 | 36 | 0 | 3 | 33 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0003 | 0/0 | 3581 | 31 | 2 | 5 | 18 | 2 | 4 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0004 | 0/0 | 3583 | 18 | 1 | 4 | 11 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0005 | 0/1 | 3579 | 18 | 2 | 11 | 3 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0006 | 0/0 | 3585 | 10 | 0 | 6 | 0 | 3 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0007 | 0/0 | 3584 | 9 | 1 | 3 | 4 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0008 | 0/0 | 3585 | 9 | 0 | 2 | 5 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0009 | 0/0 | 3583 | 8 | 2 | 0 | 4 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0010 | 0/0 | 3580 | 6 | 0 | 0 | 6 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0011 | 0/0 | 3582 | 6 | 5 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0012 | 0/0 | 3577 | 5 | 5 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0013 | 0/0 | 3580 | 5 | 0 | 0 | 4 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0014 | 0/0 | 3587 | 4 | 0 | 3 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0015 | 0/0 | 3583 | 4 | 0 | 3 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0016 | 0/0 | 3590 | 4 | 1 | 1 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0017 | 0/0 | 3588 | 4 | 0 | 0 | 4 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0018 | 0/0 | 3584 | 4 | 0 | 0 | 4 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0019 | 0/0 | 3590 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0020 | 0/0 | 3586 | 3 | 0 | 1 | 1 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0021 | 0/0 | 3593 | 3 | 2 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0022 | 0/0 | 3587 | 3 | 0 | 1 | 1 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0023 | 0/0 | 3587 | 3 | 0 | 0 | 1 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0024 | 0/0 | 3581 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0025 | 0/0 | 3581 | 3 | 1 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0026 | 0/0 | 3579 | 3 | 1 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0027 | 0/0 | 3581 | 3 | 0 | 0 | 3 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0028 | 0/0 | 3581 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0029 | 0/0 | 3589 | 2 | 1 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0030 | 0/0 | 3582 | 2 | 1 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0031 | 0/0 | 3582 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0032 | 0/0 | 3596 | 2 | 1 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0033 | 0/0 | 3594 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0034 | 0/0 | 3599 | 2 | 1 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0035 | 0/0 | 3591 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0036 | 0/0 | 3583 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0037 | 0/0 | 3580 | 2 | 0 | 1 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0038 | 0/0 | 3576 | 2 | 1 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0039 | 0/0 | 3585 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0040 | 0/0 | 3581 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0041 | 0/0 | 3591 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0042 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0043 | 0/0 | 3579 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0044 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0045 | 0/0 | 3581 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0046 | 0/0 | 3577 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0047 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0048 | 0/0 | 3577 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0049 | 0/0 | 3589 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0050 | 0/0 | 3602 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0051 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0052 | 0/0 | 3594 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0053 | 0/0 | 3590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0054 | 0/0 | 3590 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0055 | 0/0 | 3588 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0056 | 0/0 | 3593 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0057 | 0/0 | 3596 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0058 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0059 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0060 | 0/0 | 3591 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0061 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0062 | 0/0 | 3584 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0063 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0064 | 0/0 | 3590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0065 | 0/0 | 3588 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0066 | 0/0 | 3588 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0067 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0068 | 0/0 | 3584 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0069 | 0/0 | 3631 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0070 | 0/0 | 3602 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0071 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0072 | 0/0 | 3598 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0073 | 0/0 | 3602 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0074 | 0/0 | 3604 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0075 | 0/0 | 3606 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0076 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0077 | 0/0 | 3601 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0078 | 0/0 | 3595 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0079 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0080 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0081 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0082 | 0/0 | 3585 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0083 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0084 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0085 | 0/0 | 3582 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0086 | 0/0 | 3581 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0087 | 0/0 | 3580 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0088 | 0/0 | 3577 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0089 | 0/0 | 3585 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0090 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0091 | 0/0 | 3598 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0092 | 0/0 | 3592 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0093 | 0/0 | 3590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0094 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0095 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0096 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0097 | 0/0 | 3578 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0098 | 0/0 | 3584 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0099 | 0/0 | 3598 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0100 | 0/0 | 3589 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0101 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0102 | 0/0 | 3601 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0103 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0104 | 0/0 | 3586 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0105 | 0/0 | 3585 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0106 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0107 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| t0108 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| 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 | 1/0 | 6009 | 123 | 16 | 31 | 50 | 9 | 16 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0007 | 0/0 | 6009 | 7 | 6 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0022 | 0/0 | 6009 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0028 | 0/0 | 6009 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0029 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002 | 0/0 | 6009 | 59 | 2 | 10 | 31 | 4 | 12 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0023 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004 | 0/0 | 6009 | 33 | 16 | 3 | 14 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0008 | 0/0 | 6009 | 6 | 5 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0011 | 0/0 | 6009 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0018 | 0/0 | 6009 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0019 | 0/0 | 6009 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0031 | 0/0 | 6009 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003 | 0/0 | 6009 | 44 | 0 | 5 | 37 | 1 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0032 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0005c0005 | 0/1 | 6009 | 20 | 7 | 7 | 3 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006 | 0/0 | 6009 | 17 | 16 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0007c0009 | 0/0 | 6009 | 4 | 1 | 1 | 0 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0008c0010 | 0/0 | 6009 | 4 | 4 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0009c0013 | 0/0 | 6009 | 3 | 0 | 0 | 2 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0010c0012 | 0/0 | 6009 | 3 | 0 | 0 | 3 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0011c0015 | 0/0 | 6009 | 2 | 0 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0012c0014 | 0/0 | 6009 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0013c0016 | 0/0 | 6009 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0014c0017 | 0/0 | 6009 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0015c0020 | 0/0 | 5959 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0016c0021 | 0/0 | 6009 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0017c0027 | 0/0 | 6009 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0018c0025 | 0/0 | 6009 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0019c0024 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0020c0026 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0021c0030 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 9589 | 40 | 0 | 3 | 27 | 2 | 7 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0002 | 0/0 | 9586 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0003 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0004 | 0/0 | 9591 | 13 | 0 | 4 | 8 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0005 | 0/0 | 9587 | 6 | 1 | 4 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0006 | 0/0 | 9593 | 10 | 0 | 6 | 0 | 3 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0007 | 0/0 | 9592 | 7 | 0 | 2 | 4 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0008 | 0/0 | 9593 | 7 | 0 | 2 | 4 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0009 | 0/0 | 9591 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0011 | 0/0 | 9590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0013 | 0/0 | 9588 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0014 | 0/0 | 9595 | 4 | 0 | 3 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0015 | 0/0 | 9591 | 3 | 0 | 2 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0022 | 0/0 | 9595 | 2 | 0 | 0 | 1 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0030 | 0/0 | 9590 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0034 | 0/0 | 9607 | 2 | 1 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0038 | 0/0 | 9584 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0040 | 0/0 | 9589 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0043 | 0/0 | 9587 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0054 | 0/0 | 9598 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0056 | 0/0 | 9601 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0061 | 0/0 | 9597 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0070 | 0/0 | 9610 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0072 | 0/0 | 9606 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0073 | 0/0 | 9610 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0074 | 0/0 | 9612 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0075 | 0/0 | 9614 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0076 | 0/0 | 9620 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0078 | 0/0 | 9603 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0080 | 0/0 | 9597 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0085 | 0/0 | 9590 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0087 | 0/0 | 9588 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0088 | 0/0 | 9585 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0092 | 0/0 | 9600 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0094 | 0/0 | 9590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0001t0108 | 0/0 | 9602 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0007t0032 | 0/0 | 9604 | 2 | 1 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0007t0033 | 0/0 | 9602 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0007t0057 | 0/0 | 9604 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0007t0071 | 0/0 | 9608 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0007t0090 | 0/0 | 9608 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0022t0062 | 0/0 | 9592 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0028t0001 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0001c0029t0004 | 0/0 | 9591 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0001 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0003 | 0/0 | 9589 | 27 | 0 | 5 | 16 | 2 | 4 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0008 | 0/0 | 9593 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0009 | 0/0 | 9591 | 3 | 0 | 0 | 1 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0010 | 0/0 | 9588 | 5 | 0 | 0 | 5 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0020 | 0/0 | 9594 | 3 | 0 | 1 | 1 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0023 | 0/0 | 9595 | 3 | 0 | 0 | 1 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0025 | 0/0 | 9589 | 3 | 1 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0026 | 0/0 | 9587 | 3 | 1 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0027 | 0/0 | 9589 | 3 | 0 | 0 | 3 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0031 | 0/0 | 9590 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0037 | 0/0 | 9588 | 2 | 0 | 1 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0063 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0084 | 0/0 | 9591 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0086 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0002t0089 | 0/0 | 9593 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0002c0023t0003 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0004 | 0/0 | 9591 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0016 | 0/0 | 9598 | 4 | 1 | 1 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0017 | 0/0 | 9596 | 4 | 0 | 0 | 4 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0018 | 0/0 | 9592 | 4 | 0 | 0 | 4 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0021 | 0/0 | 9601 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0030 | 0/0 | 9590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0035 | 0/0 | 9599 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0039 | 0/0 | 9593 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0041 | 0/0 | 9599 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0044 | 0/0 | 9595 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0058 | 0/0 | 9611 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0083 | 0/0 | 9591 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0093 | 0/0 | 9598 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0098 | 0/0 | 9592 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0099 | 0/0 | 9606 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0100 | 0/0 | 9597 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0101 | 0/0 | 9605 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0102 | 0/0 | 9609 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0103 | 0/0 | 9602 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0104 | 0/0 | 9594 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0004t0105 | 0/0 | 9593 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0008t0007 | 0/0 | 9592 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0008t0019 | 0/0 | 9598 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0008t0059 | 0/0 | 9601 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0008t0066 | 0/0 | 9596 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0008t0067 | 0/0 | 9594 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0011t0007 | 0/0 | 9592 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0011t0042 | 0/0 | 9602 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0011t0049 | 0/0 | 9597 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0018t0019 | 0/0 | 9598 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0019t0079 | 0/0 | 9601 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0003c0031t0091 | 0/0 | 9606 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003t0002 | 0/0 | 9586 | 33 | 0 | 3 | 30 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003t0004 | 0/0 | 9591 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003t0011 | 0/0 | 9590 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003t0013 | 0/0 | 9588 | 4 | 0 | 0 | 3 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003t0021 | 0/0 | 9601 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003t0038 | 0/0 | 9584 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003t0095 | 0/0 | 9587 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0003t0097 | 0/0 | 9586 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0004c0032t0002 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0005c0005t0005 | 0/1 | 9587 | 12 | 1 | 7 | 3 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0005c0005t0012 | 0/0 | 9585 | 5 | 5 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0005c0005t0029 | 0/0 | 9597 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0005c0005t0050 | 0/0 | 9610 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0005c0005t0051 | 0/0 | 9605 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0024 | 0/0 | 9589 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0028 | 0/0 | 9589 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0036 | 0/0 | 9591 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0047 | 0/0 | 9587 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0048 | 0/0 | 9585 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0065 | 0/0 | 9596 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0068 | 0/0 | 9592 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0081 | 0/0 | 9595 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0082 | 0/0 | 9593 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0096 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0106 | 0/0 | 9591 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0006c0006t0107 | 0/0 | 9591 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0007c0009t0029 | 0/0 | 9597 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0007c0009t0052 | 0/0 | 9602 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0007c0009t0053 | 0/0 | 9598 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0007c0009t0055 | 0/0 | 9596 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0008c0010t0011 | 0/0 | 9590 | 4 | 4 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0009c0013t0001 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0009c0013t0008 | 0/0 | 9593 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0009c0013t0077 | 0/0 | 9609 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0010c0012t0003 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0010c0012t0009 | 0/0 | 9591 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0011c0015t0045 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0011c0015t0046 | 0/0 | 9585 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0012c0014t0060 | 0/0 | 9599 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0012c0014t0064 | 0/0 | 9598 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0013c0016t0001 | 0/0 | 9589 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0014c0017t0003 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0015c0020t0069 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0016c0021t0004 | 0/0 | 9591 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0017c0027t0022 | 0/0 | 9595 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0018c0025t0015 | 0/0 | 9591 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0019c0024t0031 | 0/0 | 9590 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0020c0026t0009 | 0/0 | 9591 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| a0021c0030t0010 | 0/0 | 9588 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | copy fasta | chr4 | 105141876 | 105284803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0007g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0008g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0008g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0008g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0008g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0013g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0014g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0014g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0014g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0014g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0015g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0015g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0015g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0022g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0022g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0030g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0034g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0034g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0038g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0040g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0040g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0043g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0054g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0056g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0061g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0070g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0072g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0073g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0074g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0075g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0076g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0078g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0080g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0085g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0087g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0088g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0092g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0094g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0001t0108g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0007t0032g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0007t0032g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0007t0033g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0007t0033g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0007t0057g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0007t0071g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0007t0090g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0022t0062g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0028t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0001c0029t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0008g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0009g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0009g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0010g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0010g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0020g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0020g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0020g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0023g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0023g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0023g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0025g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0025g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0025g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0026g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0026g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0026g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0027g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0027g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0027g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0031g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0037g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0037g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0063g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0084g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0086g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0002t0089g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0002c0023t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0016g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0016g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0016g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0017g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0017g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0017g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0018g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0018g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0018g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0018g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0021g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0021g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0030g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0035g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0035g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0039g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0039g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0041g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0044g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0058g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0083g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0093g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0098g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0099g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0100g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0101g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0102g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0103g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0104g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0004t0105g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0008t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0008t0019g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0008t0019g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0008t0059g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0008t0066g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0008t0067g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0011t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0011t0042g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0011t0049g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0018t0019g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0019t0079g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0003c0031t0091g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0011g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0013g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0013g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0013g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0021g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0038g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0095g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0003t0097g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0004c0032t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0012g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0012g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0029g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0050g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0005c0005t0051g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0024g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0024g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0024g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0028g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0028g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0028g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0036g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0036g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0047g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0048g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0065g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0068g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0081g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0082g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0096g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0106g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0006c0006t0107g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0007c0009t0029g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0007c0009t0052g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0007c0009t0053g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0007c0009t0055g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0008c0010t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0008c0010t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0008c0010t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0008c0010t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0009c0013t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0009c0013t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0009c0013t0077g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0010c0012t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0010c0012t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0010c0012t0009g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0011c0015t0045g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0011c0015t0046g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0012c0014t0060g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0012c0014t0064g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0013c0016t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0013c0016t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0014c0017t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0015c0020t0069g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0016c0021t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0017c0027t0022g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0018c0025t0015g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0019c0024t0031g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0020c0026t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| a0021c0030t0010g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0128 | EUR | GBR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00280 | hp1 | a0001 | c0001 | t0080 | g0298 | EUR | FIN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00280 | hp2 | a0002 | c0002 | t0020 | g0171 | EUR | FIN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00323 | hp1 | a0002 | c0002 | t0003 | g0142 | EUR | FIN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0206 | EUR | FIN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00423 | hp1 | a0009 | c0013 | t0077 | g0261 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00423 | hp2 | a0004 | c0003 | t0002 | g0026 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00438 | hp1 | a0004 | c0003 | t0002 | g0108 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00544 | hp1 | a0004 | c0003 | t0002 | g0085 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0178 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00558 | hp1 | a0001 | c0001 | t0088 | g0278 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00558 | hp2 | a0002 | c0002 | t0010 | g0149 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00609 | hp1 | a0002 | c0002 | t0023 | g0160 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00609 | hp2 | a0004 | c0003 | t0002 | g0314 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0205 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00642 | hp2 | a0001 | c0001 | t0056 | g0194 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00673 | hp2 | a0019 | c0024 | t0031 | g0139 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00735 | hp1 | a0002 | c0002 | t0020 | g0172 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00735 | hp2 | a0001 | c0007 | t0032 | g0116 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00738 | hp1 | a0002 | c0002 | t0025 | g0131 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00738 | hp2 | a0007 | c0009 | t0029 | g0057 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0196 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01070 | hp1 | a0004 | c0003 | t0021 | g0117 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01070 | hp2 | a0005 | c0005 | t0005 | g0041 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01071 | hp1 | a0005 | c0005 | t0005 | g0040 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01071 | hp2 | a0004 | c0003 | t0002 | g0248 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01074 | hp2 | a0004 | c0003 | t0002 | g0118 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01081 | hp1 | a0004 | c0003 | t0038 | g0107 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01081 | hp2 | a0001 | c0001 | t0072 | g0022 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01099 | hp2 | a0011 | c0015 | t0046 | g0347 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01106 | hp1 | a0001 | c0001 | t0014 | g0215 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01106 | hp2 | a0005 | c0005 | t0005 | g0058 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01109 | hp1 | a0003 | c0004 | t0041 | g0074 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0319 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0265 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01169 | hp2 | a0002 | c0002 | t0086 | g0166 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01175 | hp1 | a0003 | c0008 | t0007 | g0046 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0212 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01192 | hp1 | a0006 | c0006 | t0048 | g0003 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01192 | hp2 | a0003 | c0004 | t0099 | g0064 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01243 | hp2 | a0003 | c0004 | t0016 | g0073 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0200 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0247 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01256 | hp1 | a0001 | c0001 | t0014 | g0210 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01256 | hp2 | a0002 | c0002 | t0003 | g0132 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0204 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01257 | hp2 | a0005 | c0005 | t0005 | g0051 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01258 | hp1 | a0001 | c0001 | t0014 | g0208 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01258 | hp2 | a0005 | c0005 | t0005 | g0052 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0187 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01261 | hp2 | a0002 | c0002 | t0037 | g0136 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01346 | hp2 | a0002 | c0002 | t0003 | g0145 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01358 | hp1 | a0005 | c0005 | t0005 | g0059 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0177 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01361 | hp1 | a0001 | c0001 | t0087 | g0028 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01361 | hp2 | a0002 | c0002 | t0084 | g0075 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01496 | hp1 | a0001 | c0028 | t0001 | g0239 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01496 | hp2 | a0017 | c0027 | t0022 | g0255 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0264 | EUR | IBS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01516 | hp2 | a0002 | c0002 | t0037 | g0148 | EUR | IBS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0263 | EUR | IBS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0211 | EUR | IBS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01884 | hp1 | a0001 | c0001 | t0108 | g0002 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01884 | hp2 | a0001 | c0001 | t0078 | g0061 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01891 | hp1 | a0003 | c0004 | t0021 | g0034 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01891 | hp2 | a0007 | c0009 | t0053 | g0056 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01928 | hp2 | a0018 | c0025 | t0015 | g0249 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01943 | hp1 | a0004 | c0003 | t0002 | g0088 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0300 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0191 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01975 | hp2 | a0005 | c0005 | t0005 | g0030 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0190 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0195 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0168 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02004 | hp1 | a0001 | c0001 | t0015 | g0291 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02004 | hp2 | a0001 | c0001 | t0073 | g0025 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02015 | hp1 | a0004 | c0003 | t0002 | g0079 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0308 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02027 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02055 | hp1 | a0006 | c0006 | t0024 | g0336 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02055 | hp2 | a0001 | c0007 | t0071 | g0180 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02056 | hp1 | a0002 | c0002 | t0026 | g0137 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02071 | hp1 | a0002 | c0002 | t0031 | g0165 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02071 | hp2 | a0003 | c0004 | t0017 | g0320 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0306 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02080 | hp2 | a0004 | c0003 | t0002 | g0089 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0293 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02135 | hp2 | a0004 | c0003 | t0002 | g0102 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02145 | hp1 | a0008 | c0010 | t0011 | g0011 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02145 | hp2 | a0003 | c0004 | t0101 | g0066 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02155 | hp1 | a0001 | c0001 | t0007 | g0305 | EAS | CDX | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02155 | hp2 | a0005 | c0005 | t0005 | g0295 | EAS | CDX | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CDX | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02257 | hp1 | a0014 | c0017 | t0003 | g0146 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02257 | hp2 | a0003 | c0004 | t0100 | g0042 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02258 | hp1 | a0001 | c0001 | t0040 | g0184 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02258 | hp2 | a0002 | c0002 | t0025 | g0138 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02280 | hp1 | a0005 | c0005 | t0012 | g0344 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02280 | hp2 | a0001 | c0001 | t0076 | g0023 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02300 | hp1 | a0001 | c0001 | t0015 | g0271 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0214 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02451 | hp1 | a0006 | c0006 | t0068 | g0013 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02451 | hp2 | a0013 | c0016 | t0001 | g0018 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02572 | hp1 | a0006 | c0006 | t0081 | g0338 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02572 | hp2 | a0003 | c0008 | t0067 | g0045 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0270 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02602 | hp2 | a0011 | c0015 | t0045 | g0348 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02615 | hp1 | a0003 | c0004 | t0035 | g0119 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02615 | hp2 | a0005 | c0005 | t0012 | g0343 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02622 | hp1 | a0001 | c0007 | t0033 | g0036 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02622 | hp2 | a0005 | c0005 | t0005 | g0150 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02647 | hp1 | a0008 | c0010 | t0011 | g0010 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02647 | hp2 | a0003 | c0004 | t0102 | g0065 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02698 | hp2 | a0016 | c0021 | t0004 | g0346 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02723 | hp1 | a0006 | c0006 | t0036 | g0334 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02735 | hp1 | a0005 | c0005 | t0050 | g0054 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0345 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02809 | hp1 | a0001 | c0007 | t0057 | g0038 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02809 | hp2 | a0003 | c0018 | t0019 | g0325 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02818 | hp1 | a0006 | c0006 | t0082 | g0335 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02818 | hp2 | a0006 | c0006 | t0028 | g0006 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02886 | hp1 | a0003 | c0004 | t0021 | g0120 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02886 | hp2 | a0006 | c0006 | t0065 | g0341 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02922 | hp1 | a0008 | c0010 | t0011 | g0007 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0151 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02965 | hp1 | a0006 | c0006 | t0047 | g0121 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02965 | hp2 | a0001 | c0001 | t0094 | g0140 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02970 | hp1 | a0006 | c0006 | t0107 | g0005 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02970 | hp2 | a0005 | c0005 | t0012 | g0069 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0129 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02976 | hp2 | a0003 | c0004 | t0016 | g0072 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03017 | hp1 | a0004 | c0003 | t0013 | g0091 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03017 | hp2 | a0002 | c0002 | t0009 | g0143 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03041 | hp1 | a0003 | c0004 | t0030 | g0202 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03041 | hp2 | a0001 | c0001 | t0092 | g0179 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03098 | hp1 | a0005 | c0005 | t0012 | g0070 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03098 | hp2 | a0006 | c0006 | t0106 | g0001 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03130 | hp1 | a0012 | c0014 | t0064 | g0048 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03130 | hp2 | a0001 | c0001 | t0070 | g0032 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03139 | hp1 | a0006 | c0006 | t0036 | g0337 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03139 | hp2 | a0003 | c0004 | t0044 | g0063 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03195 | hp1 | a0003 | c0004 | t0035 | g0062 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03195 | hp2 | a0001 | c0001 | t0040 | g0183 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03209 | hp1 | a0003 | c0011 | t0007 | g0326 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03209 | hp2 | a0003 | c0004 | t0105 | g0050 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03225 | hp1 | a0003 | c0011 | t0042 | g0329 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0185 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03239 | hp2 | a0001 | c0001 | t0022 | g0230 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03453 | hp1 | a0005 | c0005 | t0029 | g0068 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03453 | hp2 | a0012 | c0014 | t0060 | g0049 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03486 | hp1 | a0002 | c0002 | t0026 | g0173 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03486 | hp2 | a0006 | c0006 | t0096 | g0044 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03490 | hp2 | a0005 | c0005 | t0051 | g0053 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03492 | hp1 | a0001 | c0001 | t0054 | g0188 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03540 | hp1 | a0003 | c0019 | t0079 | g0043 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03540 | hp2 | a0001 | c0022 | t0062 | g0037 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03579 | hp1 | a0001 | c0007 | t0090 | g0115 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03579 | hp2 | a0003 | c0004 | t0004 | g0033 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0299 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03654 | hp2 | a0001 | c0001 | t0034 | g0197 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03669 | hp1 | a0002 | c0002 | t0089 | g0141 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03669 | hp2 | a0007 | c0009 | t0055 | g0039 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0135 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0231 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0133 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03710 | hp1 | a0015 | c0020 | t0069 | g0156 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0199 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03831 | hp2 | a0003 | c0031 | t0091 | g0019 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03927 | hp1 | a0002 | c0002 | t0008 | g0317 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03942 | hp1 | a0002 | c0002 | t0025 | g0147 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0242 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG04115 | hp1 | a0007 | c0009 | t0052 | g0031 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG04115 | hp2 | a0001 | c0001 | t0014 | g0216 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG04184 | hp1 | a0009 | c0013 | t0001 | g0322 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG04184 | hp2 | a0002 | c0002 | t0009 | g0174 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG04199 | hp1 | a0002 | c0002 | t0023 | g0122 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG04199 | hp2 | a0001 | c0001 | t0085 | g0029 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG04228 | hp1 | a0002 | c0002 | t0023 | g0123 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18522 | hp1 | a0006 | c0006 | t0024 | g0342 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18522 | hp2 | a0003 | c0004 | t0083 | g0047 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18747 | hp1 | a0005 | c0005 | t0005 | g0294 | EAS | CHB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0276 | EAS | CHB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18906 | hp1 | a0003 | c0008 | t0066 | g0328 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18906 | hp2 | a0006 | c0006 | t0028 | g0009 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18941 | hp2 | a0004 | c0003 | t0002 | g0082 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18942 | hp1 | a0004 | c0003 | t0002 | g0110 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18942 | hp2 | a0002 | c0002 | t0010 | g0035 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18944 | hp1 | a0004 | c0003 | t0002 | g0080 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18944 | hp2 | a0003 | c0004 | t0039 | g0225 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18946 | hp2 | a0004 | c0003 | t0002 | g0113 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18947 | hp2 | a0004 | c0003 | t0002 | g0112 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18948 | hp2 | a0004 | c0003 | t0002 | g0097 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18950 | hp2 | a0004 | c0003 | t0013 | g0095 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18951 | hp1 | a0003 | c0004 | t0016 | g0222 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18951 | hp2 | a0004 | c0003 | t0002 | g0099 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18956 | hp1 | a0004 | c0003 | t0011 | g0103 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18959 | hp1 | a0004 | c0003 | t0002 | g0090 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18959 | hp2 | a0002 | c0023 | t0003 | g0144 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0301 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18960 | hp2 | a0003 | c0004 | t0018 | g0221 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18963 | hp1 | a0001 | c0001 | t0030 | g0280 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18963 | hp2 | a0004 | c0003 | t0002 | g0076 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18965 | hp1 | a0004 | c0003 | t0002 | g0105 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18969 | hp2 | a0002 | c0002 | t0010 | g0162 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18973 | hp1 | a0002 | c0002 | t0003 | g0176 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18973 | hp2 | a0003 | c0004 | t0017 | g0229 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18978 | hp1 | a0004 | c0003 | t0002 | g0092 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18978 | hp2 | a0010 | c0012 | t0009 | g0236 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0152 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18980 | hp1 | a0004 | c0003 | t0002 | g0094 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18980 | hp2 | a0005 | c0005 | t0005 | g0304 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0127 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18983 | hp1 | a0004 | c0003 | t0002 | g0084 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18983 | hp2 | a0004 | c0003 | t0002 | g0101 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18985 | hp2 | a0002 | c0002 | t0063 | g0012 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18986 | hp1 | a0002 | c0002 | t0026 | g0161 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18986 | hp2 | a0004 | c0003 | t0002 | g0087 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18987 | hp1 | a0004 | c0003 | t0002 | g0096 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18987 | hp2 | a0003 | c0004 | t0017 | g0227 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18988 | hp1 | a0004 | c0003 | t0095 | g0098 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18989 | hp1 | a0002 | c0002 | t0003 | g0153 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18989 | hp2 | a0001 | c0001 | t0008 | g0302 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18993 | hp1 | a0003 | c0004 | t0018 | g0014 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18993 | hp2 | a0001 | c0001 | t0007 | g0292 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18997 | hp1 | a0004 | c0003 | t0004 | g0315 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18998 | hp1 | a0003 | c0004 | t0017 | g0228 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19001 | hp1 | a0002 | c0002 | t0003 | g0316 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19003 | hp1 | a0002 | c0002 | t0003 | g0124 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19004 | hp1 | a0001 | c0001 | t0015 | g0269 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0126 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19007 | hp1 | a0010 | c0012 | t0009 | g0218 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19007 | hp2 | a0004 | c0003 | t0002 | g0081 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19009 | hp1 | a0002 | c0002 | t0010 | g0170 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19009 | hp2 | a0001 | c0001 | t0008 | g0303 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19010 | hp1 | a0004 | c0003 | t0002 | g0083 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19012 | hp1 | a0003 | c0004 | t0098 | g0016 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19030 | hp1 | a0003 | c0004 | t0058 | g0313 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19030 | hp2 | a0008 | c0010 | t0011 | g0008 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19043 | hp1 | a0003 | c0008 | t0019 | g0330 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19043 | hp2 | a0001 | c0001 | t0038 | g0027 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19054 | hp1 | a0002 | c0002 | t0027 | g0157 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19054 | hp2 | a0009 | c0013 | t0008 | g0220 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19056 | hp1 | a0001 | c0001 | t0022 | g0238 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19056 | hp2 | a0003 | c0004 | t0039 | g0015 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19057 | hp1 | a0004 | c0003 | t0002 | g0234 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19057 | hp2 | a0002 | c0002 | t0020 | g0201 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19058 | hp1 | a0003 | c0004 | t0018 | g0224 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19058 | hp2 | a0002 | c0002 | t0003 | g0244 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19062 | hp1 | a0004 | c0003 | t0002 | g0077 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19062 | hp2 | a0002 | c0002 | t0003 | g0245 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0243 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19064 | hp2 | a0003 | c0004 | t0104 | g0285 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19070 | hp2 | a0002 | c0002 | t0010 | g0167 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19072 | hp1 | a0004 | c0003 | t0013 | g0106 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19072 | hp2 | a0002 | c0002 | t0003 | g0318 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19075 | hp2 | a0004 | c0003 | t0004 | g0181 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19079 | hp1 | a0004 | c0003 | t0002 | g0104 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19079 | hp2 | a0002 | c0002 | t0003 | g0134 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19080 | hp1 | a0010 | c0012 | t0003 | g0182 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19080 | hp2 | a0004 | c0003 | t0002 | g0100 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19082 | hp1 | a0020 | c0026 | t0009 | g0163 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19083 | hp1 | a0003 | c0004 | t0016 | g0223 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19083 | hp2 | a0004 | c0003 | t0013 | g0086 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19084 | hp1 | a0002 | c0002 | t0003 | g0125 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19086 | hp1 | a0002 | c0002 | t0027 | g0158 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19087 | hp1 | a0004 | c0003 | t0002 | g0093 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19087 | hp2 | a0001 | c0029 | t0004 | g0277 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19088 | hp2 | a0004 | c0032 | t0002 | g0078 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19089 | hp1 | a0001 | c0001 | t0013 | g0331 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19089 | hp2 | a0003 | c0004 | t0018 | g0226 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19090 | hp2 | a0002 | c0002 | t0009 | g0164 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19091 | hp2 | a0021 | c0030 | t0010 | g0154 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19240 | hp1 | a0003 | c0011 | t0049 | g0327 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA19240 | hp2 | a0006 | c0006 | t0028 | g0004 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA20129 | hp1 | a0001 | c0001 | t0075 | g0024 | AFR | ASW | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA20129 | hp2 | a0003 | c0004 | t0093 | g0020 | AFR | ASW | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA20752 | hp1 | a0004 | c0003 | t0097 | g0109 | EUR | TSI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA20752 | hp2 | a0001 | c0001 | t0074 | g0021 | EUR | TSI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA20805 | hp2 | a0001 | c0001 | t0061 | g0213 | EUR | TSI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01123 | hp1 | a0001 | c0001 | t0043 | g0198 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0207 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02559 | hp1 | a0006 | c0006 | t0024 | g0339 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG02559 | hp2 | a0001 | c0001 | t0034 | g0060 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03471 | hp1 | a0001 | c0007 | t0033 | g0114 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG03471 | hp2 | a0005 | c0005 | t0012 | g0071 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG06807 | hp1 | a0003 | c0008 | t0019 | g0333 | AFR | USA | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| HG06807 | hp2 | a0001 | c0007 | t0032 | g0340 | AFR | USA | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA18955 | hp2 | a0002 | c0002 | t0027 | g0169 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA20300 | hp1 | a0003 | c0004 | t0103 | g0067 | AFR | USA | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | USA | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA21309 | hp1 | a0013 | c0016 | t0001 | g0017 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| NA21309 | hp2 | a0003 | c0008 | t0059 | g0324 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| homoSapiens_chm13v2 | hp1 | a0005 | c0005 | t0005 | g0055 | REF | REF | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0217 | REF | REF | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105234028
|
C | G | 2 | a0004a0008 | 49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
missense_variant | MODERATE | c.86C>G | p.Pro29Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 382/9589 | 86/6009 | 29/2002 | chr4 | 105234028 | ||
| chr4:105234042
|
C | T | 1 | a0011 | 2 | HG01099.hp2 HG02602.hp2 |
missense_variant | MODERATE | c.100C>T | p.Leu34Phe | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 396/9589 | 100/6009 | 34/2002 | chr4 | 105234042 | ||
| chr4:105234463
|
C | A | 1 | a0014 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.521C>A | p.Pro174His | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 817/9589 | 521/6009 | 174/2002 | chr4 | 105234463 | ||
| chr4:105234594
|
G | A | 3 | a0003a0011a0012 | 49 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(46): Show |
missense_variant | MODERATE | c.652G>A | p.Val218Met | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 948/9589 | 652/6009 | 218/2002 | chr4 | 105234594 | ||
| chr4:105235006
|
G | A | 1 | a0015 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1064G>A | p.Gly355Asp | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 1360/9589 | 1064/6009 | 355/2002 | chr4 | 105235006 | ||
| chr4:105235030
|
C | T | 1 | a0007 | 4 | HG00738.hp2 HG01891.hp2 HG03669.hp2 others(1): Show |
missense_variant | MODERATE | c.1088C>T | p.Pro363Leu | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 1384/9589 | 1088/6009 | 363/2002 | chr4 | 105235030 | ||
| chr4:105235666
|
C | T | 1 | a0021 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.1724C>T | p.Ala575Val | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2020/9589 | 1724/6009 | 575/2002 | chr4 | 105235666 | ||
| chr4:105236371
|
A | G | 1 | a0012 | 2 | HG03130.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.2429A>G | p.Gln810Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2725/9589 | 2429/6009 | 810/2002 | chr4 | 105236371 | ||
| chr4:105236541
|
T | C | 1 | a0016 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.2599T>C | p.Tyr867His | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2895/9589 | 2599/6009 | 867/2002 | chr4 | 105236541 | ||
| chr4:105236546
|
T | G | 1 | a0010 | 3 | NA18978.hp2 NA19007.hp1 NA19080.hp1 |
missense_variant | MODERATE | c.2604T>G | p.Phe868Leu | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2900/9589 | 2604/6009 | 868/2002 | chr4 | 105236546 | ||
| chr4:105236713
|
A | G | 1 | a0008 | 4 | HG02145.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.2771A>G | p.His924Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3067/9589 | 2771/6009 | 924/2002 | chr4 | 105236713 | ||
| chr4:105237058
|
C | T | 1 | a0009 | 3 | HG00423.hp1 HG04184.hp1 NA19054.hp2 |
missense_variant | MODERATE | c.3116C>T | p.Ser1039Leu | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3412/9589 | 3116/6009 | 1039/2002 | chr4 | 105237058 | ||
| chr4:105237193
|
A | C | 1 | a0017 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.3251A>C | p.Gln1084Pro | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3547/9589 | 3251/6009 | 1084/2002 | chr4 | 105237193 | ||
| chr4:105243754
|
A | G | 1 | a0020 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.3779A>G | p.Asn1260Ser | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/11 | 4075/9589 | 3779/6009 | 1260/2002 | chr4 | 105243754 | ||
| chr4:105272679
|
AAGCTCAG others(43): Show |
A | 1 | a0015 | 1 | HG03710.hp1 | frameshift_variant | HIGH | c.4299_4348delAGCTCA others(44): Show |
p.Glu1433fs | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/11 | 4595/9589 | 4299/6009 | 1433/2002 | chr4 | 105272679 | ||
| chr4:105275251
|
A | G | 1 | a0018 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.4741A>G | p.Asn1581Asp | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5037/9589 | 4741/6009 | 1581/2002 | chr4 | 105275251 | ||
| chr4:105275672
|
T | G | 2 | a0005a0007 | 24 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
missense_variant | MODERATE | c.5162T>G | p.Leu1721Trp | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5458/9589 | 5162/6009 | 1721/2002 | chr4 | 105275672 | ||
| chr4:105275677
|
C | T | 1 | a0016 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.5167C>T | p.Pro1723Ser | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5463/9589 | 5167/6009 | 1723/2002 | chr4 | 105275677 | ||
| chr4:105275794
|
A | G | 7 | a0002a0010a0014others(4): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
missense_variant | MODERATE | c.5284A>G | p.Ile1762Val | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5580/9589 | 5284/6009 | 1762/2002 | chr4 | 105275794 | ||
| chr4:105275843
|
A | G | 4 | a0006a0011a0013others(1): Show | 22 | HG01099.hp2 HG01192.hp1 HG02055.hp1 others(19): Show |
missense_variant | MODERATE | c.5333A>G | p.His1778Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5629/9589 | 5333/6009 | 1778/2002 | chr4 | 105275843 | ||
| chr4:105275927
|
A | G | 1 | a0019 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.5417A>G | p.His1806Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5713/9589 | 5417/6009 | 1806/2002 | chr4 | 105275927 | ||
| chr4:105275959
|
C | A | 1 | a0013 | 2 | HG02451.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.5449C>A | p.His1817Asn | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5745/9589 | 5449/6009 | 1817/2002 | chr4 | 105275959 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105233979
|
A | C | 1 | a0013c0016 | 2 | HG02451.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.37A>C | p.Arg13Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 333/9589 | 37/6009 | 13/2002 | chr4 | 105233979 | ||
| chr4:105234548
|
C | T | 1 | a0003c0031 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.606C>T | p.Asn202Asn | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 902/9589 | 606/6009 | 202/2002 | chr4 | 105234548 | ||
| chr4:105235826
|
G | A | 2 | a0003c0011a0003c0018 | 4 | HG02809.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.1884G>A | p.Glu628Glu | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2180/9589 | 1884/6009 | 628/2002 | chr4 | 105235826 | ||
| chr4:105236726
|
T | C | 1 | a0004c0032 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.2784T>C | p.Phe928Phe | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3080/9589 | 2784/6009 | 928/2002 | chr4 | 105236726 | ||
| chr4:105236978
|
A | G | 1 | a0001c0029 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.3036A>G | p.Pro1012Pro | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3332/9589 | 3036/6009 | 1012/2002 | chr4 | 105236978 | ||
| chr4:105237032
|
G | A | 1 | a0003c0008 | 6 | HG01175.hp1 HG02572.hp2 HG06807.hp1 others(3): Show |
synonymous_variant | LOW | c.3090G>A | p.Gln1030Gln | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3386/9589 | 3090/6009 | 1030/2002 | chr4 | 105237032 | ||
| chr4:105237059
|
G | A | 5 | a0003c0004a0003c0008a0003c0011others(2): Show | 45 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(42): Show |
synonymous_variant | LOW | c.3117G>A | p.Ser1039Ser | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3413/9589 | 3117/6009 | 1039/2002 | chr4 | 105237059 | ||
| chr4:105237176
|
C | T | 1 | a0001c0028 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.3234C>T | p.Thr1078Thr | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3530/9589 | 3234/6009 | 1078/2002 | chr4 | 105237176 | ||
| chr4:105269705
|
T | C | 7 | a0001c0007a0001c0022a0003c0004others(4): Show | 52 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(49): Show |
synonymous_variant | LOW | c.4140T>C | p.His1380His | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/11 | 4436/9589 | 4140/6009 | 1380/2002 | chr4 | 105269705 | ||
| chr4:105275820
|
G | A | 1 | a0001c0022 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.5310G>A | p.Pro1770Pro | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5606/9589 | 5310/6009 | 1770/2002 | chr4 | 105275820 | ||
| chr4:105276039
|
C | T | 1 | a0003c0018 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.5529C>T | p.Asn1843Asn | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5825/9589 | 5529/6009 | 1843/2002 | chr4 | 105276039 | ||
| chr4:105276495
|
A | G | 1 | a0002c0023 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.5985A>G | p.Thr1995Thr | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 6281/9589 | 5985/6009 | 1995/2002 | chr4 | 105276495 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105146960
|
G | A | 1 | a0003c0004t0041 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/11 | 86983 | chr4 | 105146960 | |||||
| chr4:105146972
|
A | C | 4 | a0001c0001t0108a0006c0006t0028a0006c0006t0106others(1): Show | 6 | HG01884.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-200A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/11 | 86971 | chr4 | 105146972 | |||||
| chr4:105190388
|
T | C | 1 | a0003c0011t0042 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-164T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | 43555 | chr4 | 105190388 | |||||
| chr4:105190394
|
T | C | 1 | a0001c0001t0043 | 1 | HG01123.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-158T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | chr4 | 105190394 | ||||||
| chr4:105190420
|
A | G | 1 | a0003c0004t0105 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | 43523 | chr4 | 105190420 | |||||
| chr4:105190424
|
A | G | 1 | a0001c0001t0040 | 2 | HG02258.hp1 HG03195.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | chr4 | 105190424 | ||||||
| chr4:105190466
|
G | C | 1 | a0003c0004t0044 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | 43477 | chr4 | 105190466 | |||||
| chr4:105276593
|
G | A | 7 | a0006c0006t0028a0006c0006t0047a0006c0006t0048others(4): Show | 9 | HG01099.hp2 HG01192.hp1 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*74G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 74 | chr4 | 105276593 | |||||
| chr4:105276681
|
T | A | 1 | a0003c0011t0049 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 162 | chr4 | 105276681 | |||||
| chr4:105276779
|
C | T | 5 | a0006c0006t0028a0006c0006t0047a0006c0006t0048others(2): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*260C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 260 | chr4 | 105276779 | |||||
| chr4:105276804
|
T | A | 1 | a0003c0011t0049 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*285T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 285 | chr4 | 105276804 | |||||
| chr4:105276807
|
T | C | 1 | a0003c0011t0049 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*288T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 288 | chr4 | 105276807 | |||||
| chr4:105276837
|
A | ATC | 3 | a0003c0004t0039a0003c0004t0099a0003c0004t0100 | 4 | HG01192.hp2 HG02257.hp2 NA18944.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*320dupTC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 321 | INFO_REALIGN_3_PRIME | chr4 | 105276837 | ||||
| chr4:105276838
|
T | TC | 19 | a0001c0001t0007a0001c0001t0030a0001c0001t0108others(16): Show | 32 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*330dupC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276838
|
T | TCC | 11 | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(8): Show | 25 | HG00323.hp2 HG01106.hp1 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*329_*330dupCC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276838
|
T | TCCCCCCC others(3): Show |
1 | a0001c0001t0056 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321_*330dupCCCCCC others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276838
|
T | TCCCCCCC others(4): Show |
2 | a0001c0001t0054a0007c0009t0055 | 2 | HG03492.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*320_*330dupCCCCCC others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276838
|
T | TCCCCCCC others(5): Show |
2 | a0005c0005t0029a0007c0009t0029 | 2 | HG00738.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330_*331insCCCCCC others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276838
|
T | TCCCCCCC others(6): Show |
2 | a0007c0009t0052a0007c0009t0053 | 2 | HG01891.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330_*331insCCCCCC others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276838
|
T | TCCCCCCC others(13): Show |
1 | a0005c0005t0051 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330_*331insCCCCCC others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276838
|
T | TCCCCCCC others(18): Show |
1 | a0005c0005t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330_*331insCCCCCC others(19): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276838
|
TC | T | 18 | a0001c0001t0002a0001c0001t0011a0001c0001t0013others(15): Show | 58 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*330delC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 330 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | ||||
| chr4:105276839
|
C | CT | 8 | a0003c0004t0016a0003c0004t0017a0003c0004t0018others(5): Show | 17 | HG01243.hp2 HG02071.hp2 HG02145.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*320_*321insT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 321 | chr4 | 105276839 | |||||
| chr4:105276846
|
C | A | 1 | a0003c0004t0098 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 327 | chr4 | 105276846 | |||||
| chr4:105277168
|
A | T | 1 | a0001c0007t0090 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 649 | chr4 | 105277168 | |||||
| chr4:105277179
|
A | G | 2 | a0002c0002t0027a0002c0002t0089 | 4 | HG03669.hp1 NA18955.hp2 NA19054.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*660A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 660 | chr4 | 105277179 | |||||
| chr4:105277601
|
C | T | 2 | a0011c0015t0045a0011c0015t0046 | 2 | HG01099.hp2 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1082C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1082 | chr4 | 105277601 | |||||
| chr4:105278071
|
A | ATAAAGAA others(43): Show |
1 | a0015c0020t0069 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1554_*1603dupAAAG others(46): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1604 | INFO_REALIGN_3_PRIME | chr4 | 105278071 | ||||
| chr4:105278171
|
C | CAT | 27 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(24): Show | 67 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1683_*1684dupAT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATACATA others(5): Show |
3 | a0001c0001t0108a0001c0007t0033a0001c0007t0057 | 4 | HG01884.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1655_*1656insCATA others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATACATA others(7): Show |
1 | a0001c0007t0032 | 2 | HG00735.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1655_*1656insCATA others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATACATA others(11): Show |
2 | a0001c0007t0071a0001c0007t0090 | 2 | HG02055.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1655_*1656insCATA others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATACATA others(13): Show |
1 | a0001c0001t0070 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1655_*1656insCATA others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATAT | 10 | a0001c0001t0008a0001c0001t0014a0002c0002t0008others(7): Show | 21 | HG00280.hp2 HG00735.hp1 HG01106.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1681_*1684dupATAT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATATAT | 10 | a0001c0001t0022a0001c0001t0061a0002c0002t0023others(7): Show | 16 | HG00609.hp1 HG01496.hp2 HG02071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1679_*1684dupATAT others(2): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATATATA others(1): Show |
7 | a0001c0001t0080a0003c0004t0016a0003c0008t0019others(4): Show | 11 | HG00280.hp1 HG01243.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1677_*1684dupATAT others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATATATA others(3): Show |
4 | a0003c0004t0035a0003c0004t0041a0003c0004t0093others(1): Show | 5 | HG01109.hp1 HG02615.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1675_*1684dupATAT others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATATATA others(5): Show |
6 | a0001c0001t0092a0003c0004t0021a0003c0004t0103others(3): Show | 7 | HG01070.hp1 HG01891.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1673_*1684dupATAT others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATATATA others(7): Show |
1 | a0001c0001t0078 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1671_*1684dupATAT others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATATATA others(11): Show |
2 | a0001c0001t0034a0003c0031t0091 | 3 | HG02559.hp2 HG03654.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1667_*1684dupATAT others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
C | CATATATA others(13): Show |
2 | a0003c0004t0058a0009c0013t0077 | 2 | HG00423.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1665_*1684dupATAT others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
CAT | C | 16 | a0001c0001t0002a0001c0001t0005a0001c0001t0043others(13): Show | 71 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1683_*1684delAT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1683 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278171
|
CATAT | C | 12 | a0001c0001t0038a0001c0001t0088a0004c0003t0038others(9): Show | 16 | HG00558.hp1 HG00738.hp2 HG01081.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1681_*1684delATAT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1681 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | ||||
| chr4:105278203
|
T | TATATATA others(8): Show |
2 | a0003c0004t0099a0003c0004t0101 | 2 | HG01192.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | |||||
| chr4:105278203
|
T | TATATATA others(10): Show |
1 | a0001c0001t0072 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(13): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | |||||
| chr4:105278203
|
T | TATATATA others(12): Show |
1 | a0003c0004t0102 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(15): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | |||||
| chr4:105278203
|
T | TATATATA others(14): Show |
1 | a0001c0001t0073 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(17): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | |||||
| chr4:105278203
|
T | TATATATA others(16): Show |
1 | a0001c0001t0074 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(19): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | |||||
| chr4:105278203
|
T | TATATATA others(18): Show |
1 | a0001c0001t0075 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(21): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | |||||
| chr4:105278203
|
T | TATATATA others(24): Show |
1 | a0001c0001t0076 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(27): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | |||||
| chr4:105278276
|
A | G | 1 | a0002c0002t0086 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1757A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1757 | chr4 | 105278276 | |||||
| chr4:105278348
|
A | T | 25 | a0001c0001t0003a0001c0001t0009a0001c0001t0094others(22): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1829A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1829 | chr4 | 105278348 | |||||
| chr4:105278358
|
A | G | 1 | a0001c0001t0092 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1839A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1839 | chr4 | 105278358 | |||||
| chr4:105278405
|
T | TA | 10 | a0001c0001t0070a0001c0001t0085a0001c0001t0087others(7): Show | 12 | HG00735.hp2 HG01361.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1896dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1897 | INFO_REALIGN_3_PRIME | chr4 | 105278405 | ||||
| chr4:105278631
|
A | G | 1 | a0004c0003t0097 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2112A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2112 | chr4 | 105278631 | |||||
| chr4:105279048
|
C | G | 1 | a0003c0031t0091 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2529C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2529 | chr4 | 105279048 | |||||
| chr4:105279077
|
T | C | 8 | a0006c0006t0024a0006c0006t0036a0006c0006t0065others(5): Show | 11 | HG02055.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2558T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2558 | chr4 | 105279077 | |||||
| chr4:105279478
|
A | G | 2 | a0002c0002t0025a0002c0002t0084 | 4 | HG00738.hp1 HG01361.hp2 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2959A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2959 | chr4 | 105279478 | |||||
| chr4:105279511
|
C | T | 6 | a0003c0004t0058a0003c0004t0083a0003c0004t0105others(3): Show | 6 | HG03130.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2992C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2992 | chr4 | 105279511 | |||||
| chr4:105279571
|
C | T | 1 | a0001c0001t0088 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3052C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 3052 | chr4 | 105279571 | |||||
| chr4:105279624
|
C | T | 2 | a0006c0006t0028a0006c0006t0107 | 4 | HG02818.hp2 HG02970.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3105C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 3105 | chr4 | 105279624 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105146998
|
T | C | 11 | a0001c0001t0108g0002a0006c0006t0028g0004a0006c0006t0028g0006others(8): Show | 11 | HG01192.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+19T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105146998 | ||||||
| chr4:105147297
|
T | G | 1 | a0002c0002t0063g0012 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-193+318T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147297 | ||||||
| chr4:105147341
|
C | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+362C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147341 | ||||||
| chr4:105147342
|
A | G | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+363A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147342 | ||||||
| chr4:105147343
|
C | T | 1 | a0002c0002t0003g0345 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-193+364C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147343 | ||||||
| chr4:105147489
|
C | T | 11 | a0001c0007t0032g0340a0005c0005t0012g0343a0005c0005t0012g0344others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+510C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147489 | ||||||
| chr4:105147545
|
A | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+566A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147545 | ||||||
| chr4:105147574
|
G | GT | 11 | a0001c0001t0001g0332a0001c0001t0013g0331a0003c0008t0019g0330others(8): Show | 11 | HG02145.hp1 HG02809.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+605dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105147574 | |||||
| chr4:105147584
|
T | C | 1 | a0006c0006t0068g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-193+605T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147584 | ||||||
| chr4:105147797
|
T | C | 3 | a0003c0004t0018g0014a0003c0004t0039g0015a0003c0004t0098g0016 | 3 | NA18993.hp1 NA19012.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-193+818T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147797 | ||||||
| chr4:105147841
|
A | AG | 12 | a0001c0001t0001g0321a0001c0001t0004g0323a0001c0001t0006g0319others(9): Show | 12 | HG00609.hp2 HG01109.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.-193+867dupG | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105147841 | |||||
| chr4:105147856
|
G | T | 103 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(100): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-193+877G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147856 | ||||||
| chr4:105147873
|
G | GA | 347 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(344): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.-193+894_-193+895i others(3): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147873 | ||||||
| chr4:105147898
|
G | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-193+919G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147898 | ||||||
| chr4:105148059
|
T | TAC | 10 | a0001c0001t0001g0219a0001c0001t0072g0022a0001c0001t0073g0025others(7): Show | 10 | HG00423.hp2 HG01081.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-193+1103_-193+110 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105148059 | |||||
| chr4:105148082
|
A | C | 16 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+1103A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148082 | ||||||
| chr4:105148155
|
T | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+1176T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148155 | ||||||
| chr4:105148648
|
T | G | 2 | a0003c0004t0093g0020a0003c0031t0091g0019 | 2 | HG03831.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-193+1669T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148648 | ||||||
| chr4:105148715
|
T | A | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-193+1736T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148715 | ||||||
| chr4:105148754
|
G | A | 2 | a0001c0001t0085g0029a0001c0001t0087g0028 | 2 | HG01361.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-193+1775G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148754 | ||||||
| chr4:105148762
|
C | T | 1 | a0002c0002t0020g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-193+1783C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148762 | ||||||
| chr4:105148814
|
G | A | 1 | a0005c0005t0005g0030 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-193+1835G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148814 | ||||||
| chr4:105148848
|
T | C | 1 | a0007c0009t0052g0031 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-193+1869T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148848 | ||||||
| chr4:105148970
|
C | A | 1 | a0001c0001t0070g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-193+1991C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148970 | ||||||
| chr4:105149048
|
C | G | 1 | a0003c0004t0098g0016 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-193+2069C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149048 | ||||||
| chr4:105149069
|
G | A | 8 | a0003c0008t0019g0330a0003c0008t0019g0333a0003c0008t0059g0324others(5): Show | 8 | HG02809.hp2 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.-193+2090G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149069 | ||||||
| chr4:105149092
|
A | C | 1 | a0002c0002t0003g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-193+2113A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149092 | ||||||
| chr4:105149105
|
G | A | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-193+2126G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149105 | ||||||
| chr4:105149116
|
G | T | 1 | a0003c0004t0098g0016 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-193+2137G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149116 | ||||||
| chr4:105149143
|
A | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+2164A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149143 | ||||||
| chr4:105149179
|
T | C | 1 | a0002c0002t0010g0035 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-193+2200T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149179 | ||||||
| chr4:105149283
|
T | G | 4 | a0001c0001t0038g0027a0003c0031t0091g0019a0011c0015t0045g0348others(1): Show | 4 | HG01099.hp2 HG02602.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+2304T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149283 | ||||||
| chr4:105149474
|
A | G | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0004g0309others(1): Show | 4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+2495A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149474 | ||||||
| chr4:105149573
|
T | C | 3 | a0001c0007t0033g0036a0001c0007t0057g0038a0001c0022t0062g0037 | 3 | HG02622.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+2594T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149573 | ||||||
| chr4:105149907
|
A | G | 137 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(134): Show | 137 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-193+2928A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149907 | ||||||
| chr4:105150231
|
G | A | 1 | a0009c0013t0008g0220 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-193+3252G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150231 | ||||||
| chr4:105150440
|
T | A | 46 | a0001c0001t0034g0060a0001c0001t0072g0022a0001c0001t0073g0025others(43): Show | 46 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.-193+3461T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150440 | ||||||
| chr4:105150570
|
G | A | 13 | a0003c0004t0016g0222a0003c0004t0016g0223a0003c0004t0017g0227others(10): Show | 13 | HG02071.hp2 NA18944.hp2 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-193+3591G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150570 | ||||||
| chr4:105150702
|
C | G | 1 | a0004c0003t0004g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-193+3723C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150702 | ||||||
| chr4:105150704
|
A | C | 1 | a0004c0003t0004g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-193+3725A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150704 | ||||||
| chr4:105150863
|
C | G | 346 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(343): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.-193+3884C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150863 | ||||||
| chr4:105150952
|
G | A | 1 | a0003c0004t0004g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-193+3973G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150952 | ||||||
| chr4:105150999
|
G | T | 15 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(12): Show | 15 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.-193+4020G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150999 | ||||||
| chr4:105151045
|
C | T | 1 | a0008c0010t0011g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-193+4066C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151045 | ||||||
| chr4:105151046
|
G | A | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+4067G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151046 | ||||||
| chr4:105151107
|
C | T | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+4128C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151107 | ||||||
| chr4:105151142
|
G | T | 1 | a0001c0007t0071g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-193+4163G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151142 | ||||||
| chr4:105151179
|
G | T | 1 | a0003c0004t0017g0320 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-193+4200G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151179 | ||||||
| chr4:105151299
|
C | T | 17 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(14): Show | 17 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-193+4320C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151299 | ||||||
| chr4:105151328
|
G | A | 49 | a0001c0001t0001g0111a0001c0001t0013g0331a0001c0007t0032g0116others(46): Show | 49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-193+4349G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151328 | ||||||
| chr4:105151426
|
C | T | 16 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+4447C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151426 | ||||||
| chr4:105151791
|
G | A | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-193+4812G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151791 | ||||||
| chr4:105151837
|
C | T | 1 | a0003c0004t0004g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-193+4858C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151837 | ||||||
| chr4:105151838
|
G | A | 16 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+4859G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151838 | ||||||
| chr4:105151849
|
T | C | 1 | a0007c0009t0052g0031 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-193+4870T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151849 | ||||||
| chr4:105151900
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+4921C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151900 | ||||||
| chr4:105151932
|
G | A | 10 | a0004c0003t0002g0076a0004c0003t0002g0077a0004c0003t0002g0079others(7): Show | 10 | HG00544.hp1 HG02015.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.-193+4953G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151932 | ||||||
| chr4:105151958
|
C | G | 16 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+4979C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151958 | ||||||
| chr4:105151959
|
C | A | 1 | a0001c0001t0022g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-193+4980C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151959 | ||||||
| chr4:105151982
|
C | T | 1 | a0001c0001t0008g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-193+5003C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151982 | ||||||
| chr4:105152094
|
A | G | 6 | a0001c0007t0032g0340a0005c0005t0012g0343a0005c0005t0012g0344others(3): Show | 6 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-193+5115A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152094 | ||||||
| chr4:105152205
|
C | T | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-193+5226C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152205 | ||||||
| chr4:105152352
|
A | G | 105 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(102): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-193+5373A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152352 | ||||||
| chr4:105152513
|
A | G | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+5534A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152513 | ||||||
| chr4:105152546
|
G | GA | 51 | a0001c0001t0001g0111a0001c0001t0013g0331a0001c0007t0032g0116others(48): Show | 51 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.-193+5576dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105152546 | |||||
| chr4:105152578
|
TTTTC | T | 72 | a0001c0001t0001g0111a0001c0001t0001g0233a0001c0001t0004g0309others(69): Show | 72 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.-193+5619_-193+562 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105152578 | |||||
| chr4:105152595
|
TTTC | T | 171 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0219others(168): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-193+5619_-193+562 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105152595 | |||||
| chr4:105152817
|
G | A | 2 | a0001c0001t0001g0235a0004c0003t0002g0234 | 2 | NA19057.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-193+5838G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152817 | ||||||
| chr4:105152910
|
A | G | 3 | a0001c0007t0033g0036a0001c0007t0057g0038a0001c0022t0062g0037 | 3 | HG02622.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+5931A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152910 | ||||||
| chr4:105153084
|
T | C | 52 | a0001c0001t0001g0111a0001c0001t0013g0331a0001c0007t0032g0116others(49): Show | 52 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.-193+6105T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153084 | ||||||
| chr4:105153114
|
A | G | 8 | a0003c0008t0019g0330a0003c0008t0019g0333a0003c0008t0059g0324others(5): Show | 8 | HG02809.hp2 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.-193+6135A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153114 | ||||||
| chr4:105153375
|
T | C | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+6396T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153375 | ||||||
| chr4:105153420
|
TCTTGTGA others(6): Show |
T | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+6442_-193+645 others(17): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153420 | ||||||
| chr4:105153444
|
T | C | 3 | a0001c0007t0033g0036a0001c0007t0057g0038a0001c0022t0062g0037 | 3 | HG02622.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+6465T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153444 | ||||||
| chr4:105153588
|
A | G | 1 | a0002c0002t0003g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-193+6609A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153588 | ||||||
| chr4:105153669
|
T | G | 278 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(275): Show | 278 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.-193+6690T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153669 | ||||||
| chr4:105153886
|
G | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+6907G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153886 | ||||||
| chr4:105153934
|
A | G | 2 | a0001c0001t0014g0215a0001c0001t0014g0216 | 2 | HG01106.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-193+6955A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153934 | ||||||
| chr4:105154027
|
G | T | 1 | a0003c0004t0041g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-193+7048G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154027 | ||||||
| chr4:105154031
|
C | A | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-193+7052C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154031 | ||||||
| chr4:105154104
|
G | T | 1 | a0003c0004t0105g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-193+7125G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154104 | ||||||
| chr4:105154183
|
A | G | 13 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0035g0062others(10): Show | 13 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-193+7204A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154183 | ||||||
| chr4:105154341
|
T | G | 201 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0219others(198): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-193+7362T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154341 | ||||||
| chr4:105154477
|
G | T | 1 | a0001c0001t0073g0025 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-193+7498G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154477 | ||||||
| chr4:105154601
|
A | G | 55 | a0001c0001t0001g0111a0001c0001t0013g0331a0001c0007t0032g0116others(52): Show | 55 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-193+7622A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154601 | ||||||
| chr4:105154659
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+7680A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154659 | ||||||
| chr4:105154752
|
C | T | 12 | a0001c0001t0092g0179a0001c0007t0032g0340a0005c0005t0012g0343others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-193+7773C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154752 | ||||||
| chr4:105154844
|
G | A | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+7865G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154844 | ||||||
| chr4:105155000
|
G | A | 44 | a0001c0001t0001g0111a0001c0001t0013g0331a0004c0003t0002g0026others(41): Show | 44 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.-193+8021G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155000 | ||||||
| chr4:105155017
|
C | G | 14 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0035g0062others(11): Show | 14 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-193+8038C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155017 | ||||||
| chr4:105155349
|
A | G | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+8370A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155349 | ||||||
| chr4:105155372
|
G | A | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+8393G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155372 | ||||||
| chr4:105155569
|
T | A | 51 | a0001c0001t0001g0111a0001c0001t0013g0331a0001c0007t0032g0116others(48): Show | 51 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.-193+8590T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155569 | ||||||
| chr4:105155592
|
A | G | 121 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(118): Show | 121 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-193+8613A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155592 | ||||||
| chr4:105155596
|
C | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+8617C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155596 | ||||||
| chr4:105155791
|
A | G | 16 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+8812A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155791 | ||||||
| chr4:105155885
|
T | G | 1 | a0004c0003t0004g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-193+8906T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155885 | ||||||
| chr4:105156161
|
C | T | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+9182C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156161 | ||||||
| chr4:105156258
|
G | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+9279G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156258 | ||||||
| chr4:105156543
|
G | C | 1 | a0001c0001t0073g0025 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-193+9564G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156543 | ||||||
| chr4:105156752
|
A | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-193+9773A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156752 | ||||||
| chr4:105156827
|
A | G | 2 | a0004c0003t0002g0112a0004c0003t0002g0113 | 2 | NA18946.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-193+9848A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156827 | ||||||
| chr4:105156888
|
T | G | 3 | a0010c0012t0003g0182a0010c0012t0009g0218a0010c0012t0009g0236 | 3 | NA18978.hp2 NA19007.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-193+9909T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156888 | ||||||
| chr4:105156924
|
C | G | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+9945C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156924 | ||||||
| chr4:105156940
|
A | G | 43 | a0001c0001t0034g0060a0001c0001t0072g0022a0001c0001t0073g0025others(40): Show | 43 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.-193+9961A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156940 | ||||||
| chr4:105156958
|
C | T | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0004g0309others(1): Show | 4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+9979C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156958 | ||||||
| chr4:105157078
|
T | G | 1 | a0005c0005t0005g0030 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-193+10099T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157078 | ||||||
| chr4:105157083
|
A | C | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+10104A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157083 | ||||||
| chr4:105157158
|
A | G | 2 | a0003c0004t0093g0020a0003c0031t0091g0019 | 2 | HG03831.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-193+10179A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157158 | ||||||
| chr4:105157187
|
ATAT | A | 44 | a0001c0001t0034g0060a0001c0001t0072g0022a0001c0001t0073g0025others(41): Show | 44 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.-193+10211_-193+10 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105157187 | |||||
| chr4:105157330
|
T | G | 3 | a0001c0001t0001g0237a0001c0001t0022g0238a0001c0028t0001g0239 | 3 | HG01496.hp1 NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-193+10351T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157330 | ||||||
| chr4:105157521
|
C | T | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-193+10542C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157521 | ||||||
| chr4:105157650
|
A | G | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+10671A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157650 | ||||||
| chr4:105157802
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-193+10823G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157802 | ||||||
| chr4:105157846
|
T | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+10867T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157846 | ||||||
| chr4:105157955
|
G | C | 1 | a0004c0003t0002g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-193+10976G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157955 | ||||||
| chr4:105157999
|
C | T | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-193+11020C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157999 | ||||||
| chr4:105158092
|
G | T | 3 | a0003c0004t0083g0047a0012c0014t0060g0049a0012c0014t0064g0048 | 3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-193+11113G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158092 | ||||||
| chr4:105158112
|
C | T | 1 | a0001c0001t0043g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-193+11133C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158112 | ||||||
| chr4:105158143
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-193+11164G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158143 | ||||||
| chr4:105158177
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+11198C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158177 | ||||||
| chr4:105158228
|
T | A | 11 | a0001c0007t0032g0340a0005c0005t0012g0343a0005c0005t0012g0344others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+11249T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158228 | ||||||
| chr4:105158291
|
G | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+11312G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158291 | ||||||
| chr4:105158301
|
G | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+11322G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158301 | ||||||
| chr4:105158576
|
C | G | 3 | a0003c0004t0058g0313a0003c0004t0100g0042a0003c0019t0079g0043 | 3 | HG02257.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-193+11597C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158576 | ||||||
| chr4:105158596
|
G | T | 1 | a0003c0004t0021g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-193+11617G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158596 | ||||||
| chr4:105158597
|
G | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+11618G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158597 | ||||||
| chr4:105158811
|
GA | G | 7 | a0001c0001t0004g0323a0001c0001t0034g0060a0001c0001t0078g0061others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-193+11843delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105158811 | |||||
| chr4:105158929
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-193+11950C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158929 | ||||||
| chr4:105159122
|
T | C | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0004g0309others(1): Show | 4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+12143T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159122 | ||||||
| chr4:105159251
|
C | CT | 30 | a0001c0001t0001g0307a0001c0001t0001g0312a0001c0001t0001g0332others(27): Show | 30 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-193+12290dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105159251 | |||||
| chr4:105159255
|
T | C | 2 | a0003c0008t0059g0324a0003c0008t0067g0045 | 2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-193+12276T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159255 | ||||||
| chr4:105159325
|
G | A | 3 | a0001c0007t0033g0036a0001c0007t0057g0038a0001c0022t0062g0037 | 3 | HG02622.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+12346G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159325 | ||||||
| chr4:105159339
|
T | C | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+12360T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159339 | ||||||
| chr4:105159368
|
G | T | 1 | a0001c0001t0007g0306 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-193+12389G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159368 | ||||||
| chr4:105159507
|
G | C | 1 | a0001c0001t0006g0242 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-193+12528G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159507 | ||||||
| chr4:105159599
|
A | G | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-193+12620A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159599 | ||||||
| chr4:105159823
|
G | A | 1 | a0002c0002t0003g0316 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-193+12844G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159823 | ||||||
| chr4:105159970
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-193+12991C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159970 | ||||||
| chr4:105160017
|
T | A | 3 | a0002c0002t0003g0243a0002c0002t0003g0244a0002c0002t0003g0245 | 3 | NA19058.hp2 NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-193+13038T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160017 | ||||||
| chr4:105160161
|
C | T | 1 | a0003c0004t0100g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-193+13182C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160161 | ||||||
| chr4:105160401
|
G | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+13422G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160401 | ||||||
| chr4:105160411
|
T | A | 4 | a0001c0001t0001g0321a0001c0001t0004g0246a0001c0001t0008g0247others(1): Show | 4 | HG01071.hp2 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+13432T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160411 | ||||||
| chr4:105160479
|
T | C | 124 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(121): Show | 124 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-193+13500T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160479 | ||||||
| chr4:105160579
|
G | A | 3 | a0006c0006t0036g0334a0006c0006t0081g0338a0006c0006t0082g0335 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-193+13600G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160579 | ||||||
| chr4:105160633
|
C | T | 1 | a0001c0001t0014g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-193+13654C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160633 | ||||||
| chr4:105160715
|
C | A | 5 | a0001c0007t0032g0116a0001c0007t0033g0114a0001c0007t0071g0180others(2): Show | 5 | HG00735.hp2 HG01070.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+13736C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160715 | ||||||
| chr4:105160774
|
G | T | 5 | a0001c0001t0092g0179a0003c0004t0017g0227a0003c0004t0017g0228others(2): Show | 5 | HG02071.hp2 HG03041.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+13795G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160774 | ||||||
| chr4:105160774
|
GGTTT | G | 11 | a0001c0007t0032g0340a0005c0005t0012g0343a0005c0005t0012g0344others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+13812_-193+13 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105160774 | |||||
| chr4:105160907
|
C | T | 1 | a0005c0005t0012g0344 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-193+13928C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160907 | ||||||
| chr4:105160963
|
G | A | 200 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0219others(197): Show | 200 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.-193+13984G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160963 | ||||||
| chr4:105160965
|
G | A | 1 | a0001c0001t0004g0203 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-193+13986G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160965 | ||||||
| chr4:105161003
|
T | C | 1 | a0006c0006t0024g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-193+14024T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161003 | ||||||
| chr4:105161145
|
A | G | 1 | a0003c0004t0030g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-193+14166A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161145 | ||||||
| chr4:105161290
|
A | G | 2 | a0003c0008t0007g0046a0003c0008t0067g0045 | 2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-193+14311A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161290 | ||||||
| chr4:105161316
|
A | G | 12 | a0001c0001t0108g0002a0006c0006t0028g0004a0006c0006t0028g0006others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-193+14337A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161316 | ||||||
| chr4:105161324
|
T | C | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-193+14345T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161324 | ||||||
| chr4:105161802
|
A | G | 2 | a0012c0014t0060g0049a0012c0014t0064g0048 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-193+14823A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161802 | ||||||
| chr4:105161898
|
G | C | 1 | a0018c0025t0015g0249 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-193+14919G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161898 | ||||||
| chr4:105161921
|
T | TGTGTGTA others(4): Show |
1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-193+14954_-193+14 others(17): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105161921 | |||||
| chr4:105162256
|
A | G | 1 | a0004c0003t0002g0110 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-193+15277A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162256 | ||||||
| chr4:105162377
|
A | T | 2 | a0003c0008t0007g0046a0003c0008t0067g0045 | 2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-193+15398A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162377 | ||||||
| chr4:105162433
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-193+15454G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162433 | ||||||
| chr4:105162619
|
C | T | 118 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(115): Show | 118 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-193+15640C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162619 | ||||||
| chr4:105162696
|
A | T | 1 | a0001c0001t0061g0213 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-193+15717A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162696 | ||||||
| chr4:105162727
|
T | A | 9 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(6): Show | 9 | HG00140.hp1 HG00741.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.-193+15748T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162727 | ||||||
| chr4:105162834
|
G | C | 5 | a0001c0001t0072g0022a0001c0001t0073g0025a0001c0001t0074g0021others(2): Show | 5 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+15855G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162834 | ||||||
| chr4:105163392
|
T | C | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+16413T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163392 | ||||||
| chr4:105163421
|
A | G | 1 | a0001c0001t0007g0305 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-193+16442A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163421 | ||||||
| chr4:105163435
|
C | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+16456C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163435 | ||||||
| chr4:105163485
|
C | A | 1 | a0001c0001t0070g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-193+16506C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163485 | ||||||
| chr4:105163486
|
G | A | 45 | a0001c0001t0034g0060a0001c0001t0072g0022a0001c0001t0073g0025others(42): Show | 45 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.-193+16507G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163486 | ||||||
| chr4:105163506
|
C | T | 1 | a0003c0011t0042g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-193+16527C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163506 | ||||||
| chr4:105163518
|
A | C | 1 | a0003c0004t0004g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-193+16539A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163518 | ||||||
| chr4:105163621
|
C | T | 102 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(99): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-193+16642C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163621 | ||||||
| chr4:105163732
|
T | C | 1 | a0002c0002t0003g0318 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-193+16753T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163732 | ||||||
| chr4:105163734
|
G | A | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+16755G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163734 | ||||||
| chr4:105163761
|
A | T | 1 | a0005c0005t0005g0304 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-193+16782A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163761 | ||||||
| chr4:105163782
|
C | G | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+16803C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163782 | ||||||
| chr4:105163806
|
C | CGA | 4 | a0002c0002t0003g0124a0002c0002t0003g0125a0002c0002t0023g0122others(1): Show | 4 | HG04199.hp1 HG04228.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+16875_-193+16 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
C | CGAGAGA | 3 | a0001c0001t0001g0251a0002c0002t0003g0175a0002c0002t0003g0316 | 3 | NA18990.hp2 NA19001.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-193+16871_-193+16 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
C | CGAGAGAG others(3): Show |
2 | a0001c0007t0033g0036a0001c0022t0062g0037 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+16867_-193+16 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
C | CGAGAGAG others(5): Show |
1 | a0001c0001t0054g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-193+16865_-193+16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGA | C | 24 | a0001c0001t0001g0232a0001c0001t0001g0307a0001c0001t0002g0253others(21): Show | 24 | HG00323.hp1 HG00558.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-193+16875_-193+16 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGA | C | 37 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(34): Show | 37 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-193+16873_-193+16 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGA | C | 70 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(67): Show | 70 | HG00558.hp1 HG00609.hp1 HG01169.hp2 others(67): Show |
intron_variant | MODIFIER | c.-193+16871_-193+16 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGAG others(1): Show |
C | 22 | a0001c0001t0001g0241a0001c0001t0001g0297a0001c0001t0004g0203others(19): Show | 22 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-193+16869_-193+16 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGAG others(3): Show |
C | 47 | a0001c0001t0001g0250a0001c0001t0004g0209a0001c0001t0006g0206others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-193+16867_-193+16 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGAG others(5): Show |
C | 8 | a0001c0001t0001g0240a0001c0001t0007g0211a0001c0001t0070g0032others(5): Show | 8 | HG01517.hp2 HG02055.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-193+16865_-193+16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGAG others(7): Show |
C | 12 | a0001c0001t0001g0111a0001c0001t0006g0212a0003c0004t0035g0062others(9): Show | 12 | HG01109.hp1 HG01175.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-193+16863_-193+16 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGAG others(9): Show |
C | 9 | a0001c0001t0006g0214a0001c0001t0006g0319a0001c0001t0061g0213others(6): Show | 9 | HG00438.hp1 HG01074.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.-193+16861_-193+16 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGAG others(11): Show |
C | 19 | a0001c0001t0073g0025a0003c0004t0083g0047a0003c0004t0099g0064others(16): Show | 19 | HG00738.hp2 HG01192.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-193+16859_-193+16 others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGAG others(13): Show |
C | 9 | a0001c0001t0072g0022a0001c0001t0074g0021a0004c0003t0097g0109others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.-193+16857_-193+16 others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163806
|
CGAGAGAG others(15): Show |
C | 5 | a0001c0001t0034g0060a0001c0001t0075g0024a0001c0001t0076g0023others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+16855_-193+16 others(28): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | |||||
| chr4:105163830
|
AGAGAGAG others(19): Show |
A | 1 | a0005c0005t0012g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-193+16853_-193+16 others(32): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163830 | |||||
| chr4:105163832
|
AGAGAGAG others(17): Show |
A | 5 | a0003c0004t0016g0073a0005c0005t0005g0051a0005c0005t0005g0052others(2): Show | 5 | HG01106.hp2 HG01243.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+16855_-193+16 others(30): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163832 | |||||
| chr4:105163834
|
AGAGAGAG others(15): Show |
A | 1 | a0003c0004t0016g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-193+16857_-193+16 others(28): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163834 | |||||
| chr4:105163836
|
AGAGAGAG others(13): Show |
A | 2 | a0003c0008t0007g0046a0003c0008t0067g0045 | 2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-193+16859_-193+16 others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163836 | |||||
| chr4:105163838
|
AGAGAGAG others(11): Show |
A | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-193+16861_-193+16 others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163838 | |||||
| chr4:105163840
|
AGAGAGAG others(9): Show |
A | 1 | a0002c0002t0009g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-193+16863_-193+16 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163840 | |||||
| chr4:105163842
|
A | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+16863A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163842 | ||||||
| chr4:105163842
|
AGAGAGAG others(7): Show |
A | 1 | a0004c0003t0013g0106 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-193+16865_-193+16 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163842 | |||||
| chr4:105163844
|
A | T | 2 | a0003c0004t0093g0020a0011c0015t0046g0347 | 2 | HG01099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-193+16865A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163844 | ||||||
| chr4:105163846
|
A | T | 3 | a0003c0004t0093g0020a0011c0015t0045g0348a0011c0015t0046g0347 | 3 | HG01099.hp2 HG02602.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-193+16867A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163846 | ||||||
| chr4:105163847
|
G | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+16868G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163847 | ||||||
| chr4:105163848
|
A | T | 4 | a0003c0004t0093g0020a0011c0015t0045g0348a0011c0015t0046g0347others(1): Show | 4 | HG01099.hp2 HG02602.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+16869A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163848 | ||||||
| chr4:105163848
|
AGAGAGAG others(1): Show |
A | 4 | a0001c0001t0001g0321a0001c0001t0004g0246a0001c0001t0008g0247others(1): Show | 4 | HG01071.hp2 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+16871_-193+16 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163848 | |||||
| chr4:105163850
|
A | T | 8 | a0003c0004t0093g0020a0006c0006t0028g0004a0006c0006t0028g0006others(5): Show | 8 | HG01099.hp2 HG01192.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-193+16871A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163850 | ||||||
| chr4:105163851
|
G | C | 1 | a0006c0006t0047g0121 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-193+16872G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163851 | ||||||
| chr4:105163852
|
A | T | 37 | a0001c0001t0001g0250a0001c0001t0001g0266a0001c0001t0001g0267others(34): Show | 37 | HG00673.hp1 HG01099.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.-193+16873A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163852 | ||||||
| chr4:105163854
|
A | AGAGAGAG others(19): Show |
1 | a0001c0001t0056g0194 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-193+16876_-193+16 others(32): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | |||||
| chr4:105163854
|
A | AGAGAGAG others(9): Show |
1 | a0001c0001t0005g0187 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-193+16876_-193+16 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | |||||
| chr4:105163854
|
A | AGAGAGAG others(11): Show |
1 | a0001c0001t0008g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-193+16876_-193+16 others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | |||||
| chr4:105163854
|
A | AGAGAGAG others(7): Show |
2 | a0001c0001t0001g0189a0001c0001t0087g0028 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-193+16876_-193+16 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | |||||
| chr4:105163854
|
A | AGAGAGAG others(5): Show |
1 | a0001c0001t0005g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-193+16876_-193+16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | |||||
| chr4:105163854
|
A | AGAGAGAG others(3): Show |
4 | a0001c0001t0001g0192a0001c0001t0005g0191a0001c0001t0043g0198others(1): Show | 4 | HG00140.hp1 HG01123.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+16876_-193+16 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | |||||
| chr4:105163854
|
A | AGAGAGAG others(5): Show |
2 | a0001c0001t0005g0190a0001c0001t0034g0197 | 2 | HG01978.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-193+16876_-193+16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | |||||
| chr4:105163854
|
A | T | 153 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(150): Show | 153 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-193+16875A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163854 | ||||||
| chr4:105163854
|
AGTGTGTG others(7): Show |
A | 1 | a0019c0024t0031g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-193+16896_-193+16 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | |||||
| chr4:105163856
|
T | A | 4 | a0002c0002t0003g0126a0002c0002t0003g0127a0002c0002t0023g0122others(1): Show | 4 | HG04199.hp1 HG04228.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+16877T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163856 | ||||||
| chr4:105163967
|
T | A | 1 | a0001c0001t0001g0251 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-193+16988T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163967 | ||||||
| chr4:105164016
|
A | T | 1 | a0004c0003t0002g0105 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-193+17037A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164016 | ||||||
| chr4:105164044
|
C | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+17065C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164044 | ||||||
| chr4:105164172
|
A | T | 2 | a0003c0004t0016g0072a0003c0004t0016g0073 | 2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-193+17193A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164172 | ||||||
| chr4:105164235
|
G | A | 2 | a0003c0004t0035g0062a0003c0004t0044g0063 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-193+17256G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164235 | ||||||
| chr4:105164247
|
G | A | 1 | a0003c0004t0099g0064 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-193+17268G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164247 | ||||||
| chr4:105164334
|
T | A | 1 | a0006c0006t0048g0003 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-193+17355T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164334 | ||||||
| chr4:105164349
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-193+17370G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164349 | ||||||
| chr4:105164367
|
C | A | 1 | a0019c0024t0031g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-193+17388C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164367 | ||||||
| chr4:105164617
|
T | C | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+17638T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164617 | ||||||
| chr4:105164624
|
T | C | 2 | a0002c0002t0020g0171a0002c0002t0020g0172 | 2 | HG00280.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-193+17645T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164624 | ||||||
| chr4:105164630
|
G | A | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-193+17651G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164630 | ||||||
| chr4:105164931
|
C | A | 1 | a0002c0002t0003g0243 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-193+17952C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164931 | ||||||
| chr4:105165028
|
T | C | 1 | a0004c0003t0097g0109 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-193+18049T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165028 | ||||||
| chr4:105165145
|
C | T | 102 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(99): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-193+18166C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165145 | ||||||
| chr4:105165203
|
C | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+18224C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165203 | ||||||
| chr4:105165237
|
G | T | 1 | a0003c0019t0079g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-193+18258G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165237 | ||||||
| chr4:105165256
|
A | T | 11 | a0001c0007t0032g0340a0005c0005t0012g0343a0005c0005t0012g0344others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+18277A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165256 | ||||||
| chr4:105165320
|
G | A | 1 | a0003c0008t0007g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-193+18341G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165320 | ||||||
| chr4:105165331
|
G | A | 4 | a0004c0003t0002g0088a0004c0003t0002g0110a0004c0003t0002g0118others(1): Show | 4 | HG01074.hp2 HG01081.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+18352G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165331 | ||||||
| chr4:105165370
|
C | T | 1 | a0003c0004t0083g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-193+18391C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165370 | ||||||
| chr4:105165371
|
G | A | 1 | a0001c0001t0007g0211 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-193+18392G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165371 | ||||||
| chr4:105165617
|
C | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+18638C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165617 | ||||||
| chr4:105166060
|
T | C | 121 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(118): Show | 121 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-193+19081T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166060 | ||||||
| chr4:105166498
|
C | A | 16 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+19519C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166498 | ||||||
| chr4:105166498
|
C | T | 3 | a0003c0004t0058g0313a0003c0004t0100g0042a0003c0019t0079g0043 | 3 | HG02257.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-193+19519C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166498 | ||||||
| chr4:105166531
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+19552C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166531 | ||||||
| chr4:105166545
|
G | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+19566G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166545 | ||||||
| chr4:105166610
|
G | GA | 45 | a0001c0001t0002g0253a0001c0001t0013g0331a0004c0003t0002g0026others(42): Show | 45 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-193+19640dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105166610 | |||||
| chr4:105166620
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-193+19641G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166620 | ||||||
| chr4:105166620
|
GAAAA | G | 5 | a0001c0001t0072g0022a0001c0001t0073g0025a0001c0001t0074g0021others(2): Show | 5 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+19647_-193+19 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105166620 | |||||
| chr4:105166621
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-193+19642A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166621 | ||||||
| chr4:105166665
|
A | G | 106 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(103): Show | 106 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-193+19686A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166665 | ||||||
| chr4:105166786
|
T | C | 1 | a0001c0001t0087g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-193+19807T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166786 | ||||||
| chr4:105166875
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-193+19896A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166875 | ||||||
| chr4:105166894
|
T | A | 118 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(115): Show | 118 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-193+19915T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166894 | ||||||
| chr4:105167001
|
C | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+20022C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167001 | ||||||
| chr4:105167135
|
T | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+20156T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167135 | ||||||
| chr4:105167326
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+20347A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167326 | ||||||
| chr4:105167342
|
A | G | 1 | a0001c0001t0004g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-193+20363A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167342 | ||||||
| chr4:105167441
|
TGTA | T | 7 | a0001c0007t0032g0340a0003c0004t0093g0020a0005c0005t0012g0343others(4): Show | 7 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-193+20466_-193+20 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105167441 | |||||
| chr4:105167511
|
A | G | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+20532A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167511 | ||||||
| chr4:105167890
|
G | A | 19 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0021g0120others(16): Show | 19 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-193+20911G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167890 | ||||||
| chr4:105167896
|
T | C | 1 | a0001c0001t0005g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-193+20917T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167896 | ||||||
| chr4:105167923
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-193+20944C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167923 | ||||||
| chr4:105167995
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-193+21016A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167995 | ||||||
| chr4:105168026
|
C | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+21047C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168026 | ||||||
| chr4:105168172
|
A | G | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-193+21193A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168172 | ||||||
| chr4:105168222
|
C | T | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+21243C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168222 | ||||||
| chr4:105168405
|
T | C | 1 | a0003c0004t0004g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-193+21426T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168405 | ||||||
| chr4:105168498
|
C | A | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-193+21519C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168498 | ||||||
| chr4:105168580
|
T | A | 1 | a0001c0001t0007g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-193+21601T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168580 | ||||||
| chr4:105168581
|
A | T | 103 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(100): Show | 103 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-193+21602A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168581 | ||||||
| chr4:105168833
|
T | C | 1 | a0003c0019t0079g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-192-21527T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168833 | ||||||
| chr4:105169398
|
G | T | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-192-20962G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169398 | ||||||
| chr4:105169488
|
C | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-20872C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169488 | ||||||
| chr4:105169892
|
T | C | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-192-20468T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169892 | ||||||
| chr4:105169925
|
C | A | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-192-20435C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169925 | ||||||
| chr4:105169925
|
C | CTG | 34 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(31): Show | 34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-192-20435_-192-20 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169925 | ||||||
| chr4:105169926
|
C | T | 34 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(31): Show | 34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-192-20434C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169926 | ||||||
| chr4:105169927
|
C | T | 34 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(31): Show | 34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-192-20433C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169927 | ||||||
| chr4:105170017
|
C | A | 2 | a0012c0014t0060g0049a0012c0014t0064g0048 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-192-20343C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170017 | ||||||
| chr4:105170067
|
T | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-20293T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170067 | ||||||
| chr4:105170095
|
T | C | 33 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(30): Show | 33 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.-192-20265T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170095 | ||||||
| chr4:105170109
|
G | A | 42 | a0001c0001t0001g0111a0001c0001t0013g0331a0004c0003t0002g0026others(39): Show | 42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-192-20251G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170109 | ||||||
| chr4:105170178
|
T | C | 1 | a0010c0012t0009g0236 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-192-20182T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170178 | ||||||
| chr4:105170299
|
C | A | 31 | a0003c0004t0016g0222a0003c0004t0016g0223a0003c0004t0017g0227others(28): Show | 31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-20061C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170299 | ||||||
| chr4:105170435
|
A | G | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-192-19925A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170435 | ||||||
| chr4:105170788
|
T | C | 1 | a0001c0001t0008g0301 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-192-19572T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170788 | ||||||
| chr4:105170789
|
T | C | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-19571T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170789 | ||||||
| chr4:105170821
|
G | A | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-192-19539G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170821 | ||||||
| chr4:105170919
|
C | T | 2 | a0001c0001t0002g0254a0001c0001t0004g0296 | 2 | NA19070.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-192-19441C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170919 | ||||||
| chr4:105170963
|
A | C | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-19397A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170963 | ||||||
| chr4:105170966
|
A | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-19394A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170966 | ||||||
| chr4:105171071
|
G | A | 6 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(3): Show | 6 | HG01192.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-192-19289G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171071 | ||||||
| chr4:105171342
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-19018A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171342 | ||||||
| chr4:105171383
|
C | T | 18 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(15): Show | 18 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-192-18977C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171383 | ||||||
| chr4:105171710
|
A | G | 2 | a0002c0002t0010g0149a0002c0002t0010g0170 | 2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-192-18650A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171710 | ||||||
| chr4:105171778
|
G | T | 2 | a0001c0001t0075g0024a0001c0001t0076g0023 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-192-18582G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171778 | ||||||
| chr4:105171865
|
T | C | 1 | a0002c0002t0003g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-192-18495T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171865 | ||||||
| chr4:105172270
|
T | G | 1 | a0001c0001t0007g0211 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-192-18090T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105172270 | ||||||
| chr4:105172321
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-18039A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105172321 | ||||||
| chr4:105172391
|
C | T | 17 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(14): Show | 17 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-192-17969C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105172391 | ||||||
| chr4:105172468
|
T | C | 1 | a0001c0001t0022g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-192-17892T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105172468 | ||||||
| chr4:105173233
|
A | C | 2 | a0001c0001t0075g0024a0001c0001t0076g0023 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-192-17127A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173233 | ||||||
| chr4:105173257
|
C | T | 2 | a0007c0009t0029g0057a0007c0009t0053g0056 | 2 | HG00738.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-192-17103C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173257 | ||||||
| chr4:105173270
|
G | A | 163 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0219others(160): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.-192-17090G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173270 | ||||||
| chr4:105173363
|
C | CA | 121 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(118): Show | 121 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-192-16982dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105173363 | |||||
| chr4:105173370
|
A | G | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-192-16990A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173370 | ||||||
| chr4:105173374
|
A | C | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-16986A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173374 | ||||||
| chr4:105173379
|
C | A | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-16981C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173379 | ||||||
| chr4:105173633
|
A | G | 1 | a0005c0005t0005g0055 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-192-16727A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173633 | ||||||
| chr4:105173662
|
G | GACATGAG others(5): Show |
1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-16687_-192-16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105173662 | |||||
| chr4:105173689
|
T | G | 18 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(15): Show | 18 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-192-16671T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173689 | ||||||
| chr4:105174062
|
T | A | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-16298T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174062 | ||||||
| chr4:105174086
|
C | T | 79 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(76): Show | 79 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-192-16274C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174086 | ||||||
| chr4:105174287
|
C | T | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-16073C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174287 | ||||||
| chr4:105174348
|
A | C | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-192-16012A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174348 | ||||||
| chr4:105174590
|
G | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-192-15770G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174590 | ||||||
| chr4:105174702
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-192-15658G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174702 | ||||||
| chr4:105174771
|
A | G | 1 | a0001c0001t0008g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-192-15589A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174771 | ||||||
| chr4:105174886
|
C | G | 1 | a0003c0004t0039g0225 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-192-15474C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174886 | ||||||
| chr4:105174903
|
A | G | 4 | a0002c0002t0027g0157a0002c0002t0027g0158a0002c0002t0027g0169others(1): Show | 4 | HG03669.hp1 NA18955.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-15457A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174903 | ||||||
| chr4:105175155
|
A | G | 4 | a0001c0007t0033g0036a0001c0007t0057g0038a0001c0022t0062g0037others(1): Show | 4 | HG02622.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192-15205A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175155 | ||||||
| chr4:105175183
|
T | G | 1 | a0001c0001t0015g0271 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-192-15177T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175183 | ||||||
| chr4:105175313
|
G | A | 1 | a0001c0001t0008g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-192-15047G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175313 | ||||||
| chr4:105175373
|
A | G | 1 | a0019c0024t0031g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-192-14987A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175373 | ||||||
| chr4:105175403
|
A | G | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-192-14957A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175403 | ||||||
| chr4:105175557
|
A | G | 9 | a0003c0004t0030g0202a0003c0008t0019g0330a0003c0008t0019g0333others(6): Show | 9 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-14803A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175557 | ||||||
| chr4:105175560
|
A | G | 9 | a0003c0004t0030g0202a0003c0008t0019g0330a0003c0008t0019g0333others(6): Show | 9 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-14800A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175560 | ||||||
| chr4:105175599
|
T | C | 11 | a0003c0004t0030g0202a0003c0008t0019g0330a0003c0008t0019g0333others(8): Show | 11 | HG02451.hp2 HG02809.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.-192-14761T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175599 | ||||||
| chr4:105175607
|
G | A | 6 | a0001c0001t0003g0159a0001c0001t0009g0129a0001c0001t0009g0151others(3): Show | 6 | HG00280.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-192-14753G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175607 | ||||||
| chr4:105175810
|
C | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-14550C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175810 | ||||||
| chr4:105175811
|
G | A | 4 | a0001c0001t0001g0321a0001c0001t0004g0246a0001c0001t0008g0247others(1): Show | 4 | HG01071.hp2 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-14549G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175811 | ||||||
| chr4:105176182
|
T | C | 278 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(275): Show | 278 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.-192-14178T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176182 | ||||||
| chr4:105176230
|
C | G | 1 | a0004c0003t0013g0106 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-192-14130C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176230 | ||||||
| chr4:105176294
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-192-14066A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176294 | ||||||
| chr4:105176295
|
A | G | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-192-14065A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176295 | ||||||
| chr4:105176445
|
A | G | 1 | a0002c0002t0003g0168 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-192-13915A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176445 | ||||||
| chr4:105176623
|
A | G | 4 | a0001c0001t0038g0027a0003c0031t0091g0019a0011c0015t0045g0348others(1): Show | 4 | HG01099.hp2 HG02602.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192-13737A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176623 | ||||||
| chr4:105177333
|
T | A | 1 | a0001c0001t0008g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-192-13027T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105177333 | ||||||
| chr4:105177875
|
G | T | 5 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(2): Show | 5 | HG02818.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-192-12485G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105177875 | ||||||
| chr4:105178004
|
C | T | 2 | a0001c0001t0007g0292a0001c0001t0008g0293 | 2 | HG02135.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-192-12356C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178004 | ||||||
| chr4:105178119
|
C | A | 1 | a0006c0006t0048g0003 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-192-12241C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178119 | ||||||
| chr4:105178154
|
G | A | 54 | a0001c0001t0001g0111a0001c0001t0013g0331a0001c0007t0032g0116others(51): Show | 54 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.-192-12206G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178154 | ||||||
| chr4:105178243
|
T | C | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-192-12117T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178243 | ||||||
| chr4:105178313
|
T | A | 4 | a0001c0001t0006g0263a0001c0001t0006g0264a0001c0001t0006g0265others(1): Show | 4 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-12047T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178313 | ||||||
| chr4:105178338
|
C | T | 2 | a0010c0012t0009g0218a0010c0012t0009g0236 | 2 | NA18978.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-192-12022C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178338 | ||||||
| chr4:105178488
|
G | T | 1 | a0004c0003t0002g0085 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-192-11872G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178488 | ||||||
| chr4:105178513
|
G | A | 1 | a0002c0002t0023g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-192-11847G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178513 | ||||||
| chr4:105178522
|
C | T | 1 | a0019c0024t0031g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-192-11838C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178522 | ||||||
| chr4:105178579
|
A | G | 4 | a0004c0003t0002g0076a0004c0003t0002g0082a0004c0003t0002g0083others(1): Show | 4 | NA18941.hp2 NA18963.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-11781A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178579 | ||||||
| chr4:105178591
|
G | A | 43 | a0001c0001t0001g0111a0001c0001t0013g0331a0004c0003t0002g0026others(40): Show | 43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-192-11769G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178591 | ||||||
| chr4:105178603
|
G | C | 1 | a0001c0007t0057g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-192-11757G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178603 | ||||||
| chr4:105178652
|
T | C | 111 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(108): Show | 111 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-192-11708T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178652 | ||||||
| chr4:105178685
|
C | G | 1 | a0002c0002t0003g0153 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-192-11675C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178685 | ||||||
| chr4:105178757
|
C | T | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-11603C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178757 | ||||||
| chr4:105179006
|
C | T | 1 | a0001c0001t0080g0298 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-192-11354C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179006 | ||||||
| chr4:105179112
|
C | T | 1 | a0001c0001t0072g0022 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-192-11248C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179112 | ||||||
| chr4:105179170
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-192-11190A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179170 | ||||||
| chr4:105179502
|
A | G | 1 | a0002c0002t0010g0167 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-192-10858A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179502 | ||||||
| chr4:105179528
|
A | G | 1 | a0001c0001t0007g0300 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-192-10832A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179528 | ||||||
| chr4:105179901
|
T | G | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-192-10459T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179901 | ||||||
| chr4:105180100
|
C | T | 1 | a0001c0001t0073g0025 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-192-10260C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105180100 | ||||||
| chr4:105180279
|
C | T | 2 | a0003c0004t0035g0062a0003c0004t0044g0063 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-192-10081C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105180279 | ||||||
| chr4:105180463
|
CTTTTAAG | C | 28 | a0001c0001t0015g0269a0005c0005t0005g0030a0005c0005t0005g0040others(25): Show | 28 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-192-9891_-192-988 others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105180463 | |||||
| chr4:105180487
|
T | G | 11 | a0001c0001t0015g0269a0005c0005t0005g0030a0005c0005t0005g0040others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-192-9873T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105180487 | ||||||
| chr4:105180642
|
A | AT | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-9705dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105180642 | |||||
| chr4:105180642
|
AT | A | 49 | a0001c0001t0002g0254a0001c0001t0004g0203a0001c0001t0004g0209others(46): Show | 49 | HG00323.hp2 HG00642.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-192-9705delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105180642 | |||||
| chr4:105180765
|
G | A | 2 | a0002c0002t0010g0149a0002c0002t0010g0170 | 2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-192-9595G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105180765 | ||||||
| chr4:105181249
|
G | C | 107 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0235others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-192-9111G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181249 | ||||||
| chr4:105181567
|
A | C | 2 | a0005c0005t0050g0054a0005c0005t0051g0053 | 2 | HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-192-8793A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181567 | ||||||
| chr4:105181618
|
T | G | 2 | a0007c0009t0052g0031a0007c0009t0055g0039 | 2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-192-8742T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181618 | ||||||
| chr4:105181783
|
T | C | 3 | a0003c0031t0091g0019a0011c0015t0045g0348a0011c0015t0046g0347 | 3 | HG01099.hp2 HG02602.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-192-8577T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181783 | ||||||
| chr4:105181785
|
C | G | 9 | a0003c0004t0030g0202a0003c0008t0019g0330a0003c0008t0019g0333others(6): Show | 9 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-8575C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181785 | ||||||
| chr4:105181834
|
T | C | 1 | a0002c0002t0089g0141 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-192-8526T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181834 | ||||||
| chr4:105181927
|
C | G | 31 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(28): Show | 31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-8433C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181927 | ||||||
| chr4:105182121
|
T | C | 1 | a0005c0005t0005g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-192-8239T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182121 | ||||||
| chr4:105182195
|
T | G | 1 | a0002c0002t0001g0130 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-192-8165T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182195 | ||||||
| chr4:105182430
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-7930T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182430 | ||||||
| chr4:105182572
|
A | G | 11 | a0001c0007t0032g0116a0001c0007t0032g0340a0001c0007t0033g0036others(8): Show | 11 | HG00735.hp2 HG01070.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-192-7788A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182572 | ||||||
| chr4:105182727
|
T | A | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-192-7633T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182727 | ||||||
| chr4:105182844
|
T | A | 1 | a0003c0004t0100g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-192-7516T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182844 | ||||||
| chr4:105182940
|
A | G | 45 | a0001c0001t0001g0111a0001c0001t0013g0331a0004c0003t0002g0026others(42): Show | 45 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-192-7420A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182940 | ||||||
| chr4:105183071
|
A | G | 1 | a0006c0006t0024g0342 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-192-7289A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105183071 | ||||||
| chr4:105183352
|
A | G | 1 | a0002c0002t0026g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-192-7008A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105183352 | ||||||
| chr4:105183900
|
A | T | 31 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(28): Show | 31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-6460A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105183900 | ||||||
| chr4:105183961
|
T | C | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-192-6399T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105183961 | ||||||
| chr4:105184102
|
C | T | 1 | a0002c0002t0086g0166 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-192-6258C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184102 | ||||||
| chr4:105184103
|
G | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-192-6257G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184103 | ||||||
| chr4:105184142
|
A | G | 278 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(275): Show | 278 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.-192-6218A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184142 | ||||||
| chr4:105184252
|
C | A | 1 | a0002c0002t0026g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-192-6108C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184252 | ||||||
| chr4:105184260
|
A | G | 1 | a0001c0001t0015g0291 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-192-6100A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184260 | ||||||
| chr4:105184462
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-192-5898G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184462 | ||||||
| chr4:105184529
|
A | G | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-192-5831A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184529 | ||||||
| chr4:105184552
|
A | T | 1 | a0002c0002t0003g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-192-5808A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184552 | ||||||
| chr4:105184594
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-5766C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184594 | ||||||
| chr4:105184718
|
G | T | 28 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(25): Show | 28 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-192-5642G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184718 | ||||||
| chr4:105184720
|
G | GGT | 34 | a0001c0001t0038g0027a0001c0001t0108g0002a0003c0004t0016g0072others(31): Show | 34 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-192-5621_-192-562 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105184720 | |||||
| chr4:105184720
|
G | GGTGT | 3 | a0003c0004t0105g0050a0003c0008t0007g0046a0003c0008t0067g0045 | 3 | HG01175.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-192-5623_-192-562 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105184720 | |||||
| chr4:105184720
|
GGTGT | G | 79 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(76): Show | 79 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-192-5623_-192-562 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105184720 | |||||
| chr4:105184832
|
A | T | 1 | a0002c0002t0003g0243 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-192-5528A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184832 | ||||||
| chr4:105184900
|
C | A | 1 | a0003c0008t0007g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-192-5460C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184900 | ||||||
| chr4:105184974
|
G | C | 79 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(76): Show | 79 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-192-5386G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184974 | ||||||
| chr4:105185055
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-5305A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185055 | ||||||
| chr4:105185119
|
G | A | 1 | a0002c0002t0025g0131 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-192-5241G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185119 | ||||||
| chr4:105185172
|
T | G | 2 | a0009c0013t0001g0322a0009c0013t0008g0220 | 2 | HG04184.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-192-5188T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185172 | ||||||
| chr4:105185196
|
C | A | 161 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0219others(158): Show | 161 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-192-5164C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185196 | ||||||
| chr4:105185197
|
G | A | 4 | a0002c0002t0027g0157a0002c0002t0027g0158a0002c0002t0027g0169others(1): Show | 4 | HG03669.hp1 NA18955.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-5163G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185197 | ||||||
| chr4:105185238
|
T | G | 10 | a0001c0007t0032g0116a0001c0007t0032g0340a0001c0007t0033g0036others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-192-5122T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185238 | ||||||
| chr4:105185544
|
G | A | 1 | a0002c0002t0084g0075 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-192-4816G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185544 | ||||||
| chr4:105185552
|
A | G | 103 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-192-4808A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185552 | ||||||
| chr4:105185568
|
C | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-4792C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185568 | ||||||
| chr4:105185643
|
G | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-192-4717G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185643 | ||||||
| chr4:105185952
|
C | T | 29 | a0001c0001t0015g0269a0004c0003t0013g0086a0005c0005t0005g0030others(26): Show | 29 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-192-4408C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185952 | ||||||
| chr4:105186334
|
C | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-192-4026C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186334 | ||||||
| chr4:105186338
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-192-4022T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186338 | ||||||
| chr4:105186347
|
C | T | 51 | a0001c0001t0013g0331a0001c0007t0032g0116a0001c0007t0032g0340others(48): Show | 51 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.-192-4013C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186347 | ||||||
| chr4:105186380
|
T | G | 1 | a0003c0004t0030g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-192-3980T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186380 | ||||||
| chr4:105186383
|
G | A | 13 | a0004c0003t0002g0076a0004c0003t0002g0077a0004c0003t0002g0079others(10): Show | 13 | HG00544.hp1 HG02015.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.-192-3977G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186383 | ||||||
| chr4:105186400
|
A | AT | 16 | a0003c0004t0016g0222a0003c0004t0016g0223a0003c0004t0017g0227others(13): Show | 16 | HG01192.hp2 HG02071.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-192-3953dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186400 | |||||
| chr4:105186400
|
A | ATT | 17 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0021g0120others(14): Show | 17 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-192-3954_-192-395 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186400 | |||||
| chr4:105186473
|
C | CT | 29 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(26): Show | 29 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-192-3867dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186473 | |||||
| chr4:105186473
|
C | CTT | 6 | a0001c0001t0006g0319a0001c0001t0014g0210a0001c0001t0014g0216others(3): Show | 6 | HG01109.hp2 HG01256.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-192-3868_-192-386 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186473 | |||||
| chr4:105186473
|
CT | C | 8 | a0002c0002t0025g0131a0003c0004t0058g0313a0003c0004t0100g0042others(5): Show | 8 | HG00738.hp1 HG02257.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-3867delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186473 | |||||
| chr4:105186562
|
G | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-192-3798G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186562 | ||||||
| chr4:105186738
|
C | T | 8 | a0001c0001t0070g0032a0006c0006t0028g0004a0006c0006t0028g0006others(5): Show | 8 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-3622C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186738 | ||||||
| chr4:105186875
|
G | C | 276 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(273): Show | 276 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.-192-3485G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186875 | ||||||
| chr4:105186900
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-3460T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186900 | ||||||
| chr4:105186922
|
C | T | 1 | a0003c0004t0017g0229 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-192-3438C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186922 | ||||||
| chr4:105186938
|
C | T | 13 | a0004c0003t0002g0099a0004c0003t0002g0100a0004c0003t0002g0101others(10): Show | 13 | HG00609.hp2 HG02135.hp2 NA18946.hp2 others(10): Show |
intron_variant | MODIFIER | c.-192-3422C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186938 | ||||||
| chr4:105187280
|
A | G | 1 | a0007c0009t0055g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-192-3080A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105187280 | ||||||
| chr4:105187482
|
T | C | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-2878T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105187482 | ||||||
| chr4:105187745
|
T | C | 29 | a0001c0001t0015g0269a0004c0003t0013g0086a0005c0005t0005g0030others(26): Show | 29 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-192-2615T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105187745 | ||||||
| chr4:105187783
|
T | C | 1 | a0001c0001t0014g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-192-2577T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105187783 | ||||||
| chr4:105188183
|
A | G | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-192-2177A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188183 | ||||||
| chr4:105188223
|
A | G | 67 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(64): Show | 67 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-192-2137A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188223 | ||||||
| chr4:105188224
|
A | G | 273 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(270): Show | 273 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.-192-2136A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188224 | ||||||
| chr4:105188283
|
A | G | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0004g0309others(1): Show | 4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192-2077A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188283 | ||||||
| chr4:105188474
|
C | T | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-192-1886C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188474 | ||||||
| chr4:105188642
|
G | A | 22 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(19): Show | 22 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-192-1718G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188642 | ||||||
| chr4:105188679
|
A | G | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-192-1681A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188679 | ||||||
| chr4:105188706
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-192-1654A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188706 | ||||||
| chr4:105188751
|
A | G | 1 | a0009c0013t0077g0261 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-192-1609A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188751 | ||||||
| chr4:105188762
|
T | G | 1 | a0009c0013t0077g0261 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-192-1598T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188762 | ||||||
| chr4:105188806
|
C | A | 1 | a0012c0014t0064g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-192-1554C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188806 | ||||||
| chr4:105188875
|
A | G | 8 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(5): Show | 8 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-1485A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188875 | ||||||
| chr4:105188895
|
G | A | 1 | a0001c0001t0005g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-192-1465G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188895 | ||||||
| chr4:105189139
|
T | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-192-1221T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189139 | ||||||
| chr4:105189204
|
GATA | G | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-1147_-192-114 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105189204 | |||||
| chr4:105189370
|
A | T | 1 | a0004c0003t0002g0076 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-192-990A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189370 | ||||||
| chr4:105189500
|
A | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-860A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189500 | ||||||
| chr4:105189504
|
TCC | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-855_-192-854d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189504 | ||||||
| chr4:105189621
|
T | A | 31 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(28): Show | 31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-739T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189621 | ||||||
| chr4:105189622
|
T | G | 1 | a0003c0011t0007g0326 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-192-738T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189622 | ||||||
| chr4:105189636
|
A | G | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-192-724A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189636 | ||||||
| chr4:105189639
|
T | C | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-721T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189639 | ||||||
| chr4:105189715
|
T | G | 1 | a0003c0008t0019g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-192-645T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189715 | ||||||
| chr4:105190114
|
G | A | 31 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(28): Show | 31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-246G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105190114 | ||||||
| chr4:105190123
|
G | T | 6 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0006g0263others(3): Show | 6 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-192-237G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105190123 | ||||||
| chr4:105190244
|
C | G | 32 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(29): Show | 32 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.-192-116C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105190244 | ||||||
| chr4:105190330
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-30T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105190330 | ||||||
| chr4:105190592
|
T | C | 34 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(31): Show | 34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-47+87T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190592 | ||||||
| chr4:105190595
|
A | G | 1 | a0010c0012t0009g0218 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47+90A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190595 | ||||||
| chr4:105190600
|
C | T | 1 | a0002c0002t0025g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-47+95C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190600 | ||||||
| chr4:105190704
|
T | C | 10 | a0001c0001t0108g0002a0006c0006t0024g0336a0006c0006t0024g0339others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+199T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190704 | ||||||
| chr4:105190821
|
A | G | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+316A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190821 | ||||||
| chr4:105191075
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0022g0230 | 2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-47+570C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191075 | ||||||
| chr4:105191103
|
T | G | 11 | a0001c0007t0032g0116a0001c0007t0032g0340a0001c0007t0033g0036others(8): Show | 11 | HG00735.hp2 HG01070.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+598T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191103 | ||||||
| chr4:105191104
|
C | T | 11 | a0001c0007t0032g0116a0001c0007t0032g0340a0001c0007t0033g0036others(8): Show | 11 | HG00735.hp2 HG01070.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+599C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191104 | ||||||
| chr4:105191179
|
G | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-47+674G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191179 | ||||||
| chr4:105191226
|
C | T | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+721C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191226 | ||||||
| chr4:105191381
|
A | C | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+876A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191381 | ||||||
| chr4:105191411
|
C | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+906C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191411 | ||||||
| chr4:105191422
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+917A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191422 | ||||||
| chr4:105191486
|
A | G | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+981A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191486 | ||||||
| chr4:105191519
|
T | G | 23 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(20): Show | 23 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47+1014T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191519 | ||||||
| chr4:105191987
|
C | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+1482C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191987 | ||||||
| chr4:105192006
|
T | G | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+1501T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192006 | ||||||
| chr4:105192411
|
T | C | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+1906T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192411 | ||||||
| chr4:105192489
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-47+1984A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192489 | ||||||
| chr4:105192526
|
T | C | 48 | a0001c0001t0001g0111a0001c0001t0013g0331a0004c0003t0002g0026others(45): Show | 48 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.-47+2021T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192526 | ||||||
| chr4:105192744
|
A | C | 1 | a0002c0002t0010g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-47+2239A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192744 | ||||||
| chr4:105192770
|
G | C | 35 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(32): Show | 35 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47+2265G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192770 | ||||||
| chr4:105192854
|
T | C | 2 | a0001c0001t0006g0206a0001c0001t0006g0207 | 2 | HG00323.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-47+2349T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192854 | ||||||
| chr4:105192914
|
A | G | 54 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(51): Show | 54 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.-47+2409A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192914 | ||||||
| chr4:105192919
|
A | G | 35 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(32): Show | 35 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47+2414A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192919 | ||||||
| chr4:105193048
|
T | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47+2543T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193048 | ||||||
| chr4:105193056
|
C | T | 1 | a0005c0005t0012g0343 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-47+2551C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193056 | ||||||
| chr4:105193218
|
G | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+2713G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193218 | ||||||
| chr4:105193543
|
G | A | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+3038G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193543 | ||||||
| chr4:105193737
|
G | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+3232G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193737 | ||||||
| chr4:105193876
|
G | A | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+3371G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193876 | ||||||
| chr4:105193994
|
C | T | 1 | a0002c0002t0003g0177 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-47+3489C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193994 | ||||||
| chr4:105194020
|
A | G | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+3515A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194020 | ||||||
| chr4:105194101
|
C | T | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-47+3596C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194101 | ||||||
| chr4:105194135
|
A | G | 33 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(30): Show | 33 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.-47+3630A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194135 | ||||||
| chr4:105194293
|
G | T | 108 | a0001c0001t0001g0111a0001c0001t0001g0219a0001c0001t0001g0233others(105): Show | 108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-47+3788G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194293 | ||||||
| chr4:105194326
|
C | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+3821C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194326 | ||||||
| chr4:105194417
|
A | C | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+3912A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194417 | ||||||
| chr4:105194551
|
A | G | 27 | a0005c0005t0005g0030a0005c0005t0005g0040a0005c0005t0005g0041others(24): Show | 27 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-47+4046A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194551 | ||||||
| chr4:105194663
|
A | C | 1 | a0007c0009t0052g0031 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47+4158A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194663 | ||||||
| chr4:105194825
|
C | T | 1 | a0003c0004t0103g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-47+4320C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194825 | ||||||
| chr4:105194938
|
C | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+4433C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194938 | ||||||
| chr4:105195019
|
A | G | 1 | a0003c0019t0079g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-47+4514A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195019 | ||||||
| chr4:105195049
|
T | C | 1 | a0001c0001t0002g0254 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-47+4544T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195049 | ||||||
| chr4:105195057
|
A | AT | 114 | a0001c0001t0001g0111a0001c0001t0001g0219a0001c0001t0001g0232others(111): Show | 114 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-47+4558dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105195057 | |||||
| chr4:105195165
|
G | A | 1 | a0004c0003t0002g0085 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-47+4660G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195165 | ||||||
| chr4:105195293
|
C | T | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+4788C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195293 | ||||||
| chr4:105195598
|
G | T | 1 | a0002c0002t0020g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+5093G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195598 | ||||||
| chr4:105195651
|
T | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+5146T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195651 | ||||||
| chr4:105195688
|
AT | A | 31 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(28): Show | 31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-47+5184delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195688 | ||||||
| chr4:105195759
|
T | C | 1 | a0002c0002t0010g0035 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-47+5254T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195759 | ||||||
| chr4:105195780
|
A | G | 1 | a0015c0020t0069g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-47+5275A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195780 | ||||||
| chr4:105195804
|
C | G | 176 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(173): Show | 176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47+5299C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195804 | ||||||
| chr4:105195967
|
C | T | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+5462C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195967 | ||||||
| chr4:105196011
|
C | G | 1 | a0001c0001t0009g0129 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-47+5506C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196011 | ||||||
| chr4:105196165
|
C | CTT | 34 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(31): Show | 34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-47+5671_-47+5672d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105196165 | |||||
| chr4:105196274
|
A | G | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47+5769A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196274 | ||||||
| chr4:105196281
|
A | G | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+5776A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196281 | ||||||
| chr4:105196377
|
GTGATGTA others(15): Show |
G | 1 | a0001c0001t0054g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-47+5873_-47+5894d others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196377 | ||||||
| chr4:105196401
|
C | A | 1 | a0001c0001t0054g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-47+5896C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196401 | ||||||
| chr4:105196625
|
C | T | 1 | a0001c0007t0071g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-47+6120C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196625 | ||||||
| chr4:105196632
|
C | G | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+6127C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196632 | ||||||
| chr4:105196762
|
C | G | 1 | a0001c0001t0054g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-47+6257C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196762 | ||||||
| chr4:105196850
|
A | G | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+6345A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196850 | ||||||
| chr4:105196900
|
T | C | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+6395T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196900 | ||||||
| chr4:105196915
|
C | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+6410C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196915 | ||||||
| chr4:105197046
|
C | A | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+6541C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197046 | ||||||
| chr4:105197114
|
T | G | 1 | a0011c0015t0045g0348 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-47+6609T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197114 | ||||||
| chr4:105197164
|
G | A | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+6659G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197164 | ||||||
| chr4:105197412
|
A | T | 1 | a0001c0001t0011g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-47+6907A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197412 | ||||||
| chr4:105197551
|
C | T | 1 | a0001c0001t0015g0291 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-47+7046C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197551 | ||||||
| chr4:105197599
|
T | C | 52 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(49): Show | 52 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-47+7094T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197599 | ||||||
| chr4:105197714
|
T | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+7209T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197714 | ||||||
| chr4:105197850
|
G | A | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+7345G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197850 | ||||||
| chr4:105198103
|
G | A | 3 | a0006c0006t0024g0339a0006c0006t0024g0342a0006c0006t0065g0341 | 3 | HG02559.hp1 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-47+7598G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198103 | ||||||
| chr4:105198680
|
G | A | 1 | a0002c0002t0020g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-47+8175G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198680 | ||||||
| chr4:105198867
|
A | G | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+8362A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198867 | ||||||
| chr4:105198873
|
A | G | 1 | a0002c0002t0003g0316 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-47+8368A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198873 | ||||||
| chr4:105198911
|
A | G | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-47+8406A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198911 | ||||||
| chr4:105199157
|
G | T | 1 | a0002c0002t0023g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-47+8652G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199157 | ||||||
| chr4:105199432
|
G | A | 6 | a0001c0007t0032g0116a0001c0007t0033g0036a0001c0007t0033g0114others(3): Show | 6 | HG00735.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+8927G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199432 | ||||||
| chr4:105199599
|
T | G | 74 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0022g0238others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-47+9094T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199599 | ||||||
| chr4:105199624
|
G | C | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+9119G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199624 | ||||||
| chr4:105199822
|
A | G | 37 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(34): Show | 37 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-47+9317A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199822 | ||||||
| chr4:105199823
|
T | C | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+9318T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199823 | ||||||
| chr4:105199920
|
G | GTT | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+9423_-47+9424d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105199920 | |||||
| chr4:105200031
|
T | C | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+9526T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200031 | ||||||
| chr4:105200259
|
T | C | 1 | a0001c0001t0040g0183 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-47+9754T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200259 | ||||||
| chr4:105200311
|
CAT | C | 10 | a0003c0004t0093g0020a0006c0006t0024g0336a0006c0006t0024g0339others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+9809_-47+9810d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105200311 | |||||
| chr4:105200388
|
ATGTT | A | 26 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(23): Show | 26 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-47+9901_-47+9904d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105200388 | |||||
| chr4:105200448
|
A | AAACTT | 39 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(36): Show | 39 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47+9943_-47+9944i others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200448 | ||||||
| chr4:105200468
|
C | G | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+9963C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200468 | ||||||
| chr4:105200628
|
GT | G | 37 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(34): Show | 37 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-47+10132delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105200628 | |||||
| chr4:105200642
|
G | GTTTTGT | 79 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-47+10166_-47+1017 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105200642 | |||||
| chr4:105200642
|
G | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+10137G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200642 | ||||||
| chr4:105200695
|
G | A | 1 | a0003c0004t0100g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-47+10190G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200695 | ||||||
| chr4:105200747
|
A | G | 39 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(36): Show | 39 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47+10242A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200747 | ||||||
| chr4:105200882
|
A | G | 1 | a0006c0006t0028g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-47+10377A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200882 | ||||||
| chr4:105200892
|
T | C | 67 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(64): Show | 67 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-47+10387T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200892 | ||||||
| chr4:105200920
|
A | G | 1 | a0002c0002t0025g0131 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-47+10415A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200920 | ||||||
| chr4:105201046
|
T | C | 8 | a0001c0007t0032g0116a0001c0007t0032g0340a0001c0007t0033g0036others(5): Show | 8 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+10541T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201046 | ||||||
| chr4:105201331
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | NA18941.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-47+10826G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201331 | ||||||
| chr4:105201381
|
G | C | 3 | a0001c0001t0015g0271a0001c0001t0015g0291a0018c0025t0015g0249 | 3 | HG01928.hp2 HG02004.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-47+10876G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201381 | ||||||
| chr4:105201448
|
T | A | 5 | a0001c0001t0007g0292a0001c0001t0008g0293a0001c0001t0008g0301others(2): Show | 5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10943T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201448 | ||||||
| chr4:105201449
|
T | C | 5 | a0001c0001t0007g0292a0001c0001t0008g0293a0001c0001t0008g0301others(2): Show | 5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10944T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201449 | ||||||
| chr4:105201450
|
G | A | 5 | a0001c0001t0007g0292a0001c0001t0008g0293a0001c0001t0008g0301others(2): Show | 5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10945G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201450 | ||||||
| chr4:105201451
|
T | A | 5 | a0001c0001t0007g0292a0001c0001t0008g0293a0001c0001t0008g0301others(2): Show | 5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10946T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201451 | ||||||
| chr4:105201452
|
T | A | 5 | a0001c0001t0007g0292a0001c0001t0008g0293a0001c0001t0008g0301others(2): Show | 5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10947T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201452 | ||||||
| chr4:105201500
|
A | G | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+10995A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201500 | ||||||
| chr4:105201542
|
G | A | 10 | a0001c0001t0108g0002a0006c0006t0024g0336a0006c0006t0024g0339others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+11037G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201542 | ||||||
| chr4:105201613
|
A | C | 5 | a0003c0008t0019g0330a0003c0008t0019g0333a0003c0008t0059g0324others(2): Show | 5 | HG02572.hp2 HG06807.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+11108A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201613 | ||||||
| chr4:105201638
|
T | C | 25 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(22): Show | 25 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.-47+11133T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201638 | ||||||
| chr4:105201732
|
C | CT | 175 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0001g0241others(172): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-47+11253dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105201732 | |||||
| chr4:105201732
|
C | CTT | 35 | a0001c0001t0007g0205a0001c0001t0014g0215a0001c0001t0014g0216others(32): Show | 35 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47+11252_-47+1125 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105201732 | |||||
| chr4:105201732
|
C | CTTT | 18 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(15): Show | 18 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+11251_-47+1125 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105201732 | |||||
| chr4:105201732
|
C | CTTTT | 7 | a0001c0001t0005g0187a0001c0001t0005g0190a0001c0001t0043g0198others(4): Show | 7 | HG01123.hp1 HG01261.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+11250_-47+1125 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105201732 | |||||
| chr4:105201732
|
C | T | 1 | a0001c0001t0007g0211 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-47+11227C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201732 | ||||||
| chr4:105201791
|
C | T | 1 | a0001c0001t0014g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-47+11286C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201791 | ||||||
| chr4:105201851
|
C | G | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+11346C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201851 | ||||||
| chr4:105201869
|
G | A | 4 | a0001c0001t0006g0263a0001c0001t0006g0264a0001c0001t0006g0265others(1): Show | 4 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+11364G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201869 | ||||||
| chr4:105201891
|
G | A | 5 | a0001c0001t0007g0292a0001c0001t0008g0293a0001c0001t0008g0301others(2): Show | 5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+11386G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201891 | ||||||
| chr4:105201915
|
G | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+11410G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201915 | ||||||
| chr4:105202041
|
C | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47+11536C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202041 | ||||||
| chr4:105202263
|
AC | A | 3 | a0002c0002t0003g0132a0002c0002t0025g0138a0015c0020t0069g0156 | 3 | HG01256.hp2 HG02258.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-47+11759delC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202263 | ||||||
| chr4:105202302
|
A | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0332 | 2 | NA18985.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-47+11797A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202302 | ||||||
| chr4:105202368
|
G | A | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47+11863G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202368 | ||||||
| chr4:105202425
|
G | C | 239 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-47+11920G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202425 | ||||||
| chr4:105202481
|
A | T | 28 | a0005c0005t0005g0030a0005c0005t0005g0040a0005c0005t0005g0041others(25): Show | 28 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-47+11976A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202481 | ||||||
| chr4:105202542
|
A | T | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+12037A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202542 | ||||||
| chr4:105202928
|
C | T | 2 | a0001c0007t0032g0340a0001c0007t0071g0180 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-47+12423C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202928 | ||||||
| chr4:105202975
|
A | G | 47 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(44): Show | 47 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.-47+12470A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202975 | ||||||
| chr4:105203048
|
T | G | 44 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(41): Show | 44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.-47+12543T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203048 | ||||||
| chr4:105203157
|
C | T | 1 | a0005c0005t0005g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-47+12652C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203157 | ||||||
| chr4:105203299
|
A | G | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47+12794A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203299 | ||||||
| chr4:105203428
|
C | G | 244 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-47+12923C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203428 | ||||||
| chr4:105203463
|
TCTTTGTA others(58): Show |
T | 45 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(42): Show | 45 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.-47+13044_-47+1310 others(69): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105203463 | |||||
| chr4:105203549
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+13044A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203549 | ||||||
| chr4:105203602
|
A | ACAATACA others(15): Show |
1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+13109_-47+1313 others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105203602 | |||||
| chr4:105203865
|
A | G | 24 | a0005c0005t0005g0030a0005c0005t0005g0040a0005c0005t0005g0041others(21): Show | 24 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-47+13360A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203865 | ||||||
| chr4:105203989
|
T | G | 4 | a0002c0002t0009g0164a0002c0002t0023g0160a0002c0002t0086g0166others(1): Show | 4 | HG00609.hp1 HG01169.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+13484T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203989 | ||||||
| chr4:105204022
|
G | A | 3 | a0005c0005t0005g0294a0005c0005t0005g0295a0005c0005t0005g0304 | 3 | HG02155.hp2 NA18747.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-47+13517G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204022 | ||||||
| chr4:105204060
|
G | A | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+13555G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204060 | ||||||
| chr4:105204130
|
C | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+13625C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204130 | ||||||
| chr4:105204152
|
C | T | 75 | a0001c0001t0001g0232a0001c0001t0003g0159a0001c0001t0009g0129others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-47+13647C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204152 | ||||||
| chr4:105204193
|
G | A | 1 | a0010c0012t0009g0236 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-47+13688G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204193 | ||||||
| chr4:105204226
|
A | T | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+13721A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204226 | ||||||
| chr4:105204228
|
A | ATAT | 3 | a0002c0002t0003g0245a0002c0002t0037g0136a0002c0002t0089g0141 | 3 | HG01261.hp2 HG03669.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-47+13723_-47+1372 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204228 | ||||||
| chr4:105204228
|
A | T | 42 | a0003c0004t0004g0033a0003c0004t0016g0222a0003c0004t0016g0223others(39): Show | 42 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.-47+13723A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204228 | ||||||
| chr4:105204230
|
T | C | 4 | a0002c0002t0003g0245a0002c0002t0037g0136a0002c0002t0089g0141others(1): Show | 4 | HG01261.hp2 HG03669.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+13725T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204230 | ||||||
| chr4:105204232
|
T | C | 5 | a0002c0002t0003g0245a0002c0002t0026g0173a0002c0002t0037g0136others(2): Show | 5 | HG01261.hp2 HG03486.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+13727T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204232 | ||||||
| chr4:105204232
|
T | TAC | 9 | a0002c0002t0003g0135a0002c0002t0003g0155a0002c0002t0003g0177others(6): Show | 9 | HG00609.hp1 HG01169.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | |||||
| chr4:105204232
|
T | TACAC | 45 | a0001c0001t0001g0232a0001c0001t0003g0159a0001c0001t0009g0129others(42): Show | 45 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | |||||
| chr4:105204232
|
T | TACACAC | 17 | a0001c0001t0001g0237a0001c0001t0022g0238a0001c0028t0001g0239others(14): Show | 17 | HG01496.hp1 HG02071.hp1 HG03704.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | |||||
| chr4:105204232
|
T | TACACACA others(1): Show |
3 | a0002c0002t0003g0142a0006c0006t0028g0009a0006c0006t0106g0001 | 3 | HG00323.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | |||||
| chr4:105204232
|
T | TACACACA others(3): Show |
2 | a0001c0001t0070g0032a0006c0006t0107g0005 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | |||||
| chr4:105204232
|
T | TACACACA others(5): Show |
1 | a0006c0006t0048g0003 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-47+13728_-47+1372 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | |||||
| chr4:105204232
|
TATAC | T | 3 | a0001c0001t0043g0198a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG01123.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+13729_-47+1373 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | |||||
| chr4:105204232
|
TATACAC | T | 13 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0005g0187others(10): Show | 13 | HG00140.hp1 HG00642.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+13729_-47+1373 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | |||||
| chr4:105204234
|
T | C | 97 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47+13729T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204234 | ||||||
| chr4:105204234
|
T | TAC | 79 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0297others(76): Show | 79 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-47+13763_-47+1376 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204234 | |||||
| chr4:105204234
|
T | TACAC | 11 | a0001c0001t0004g0262a0001c0001t0006g0206a0001c0001t0034g0060others(8): Show | 11 | HG00323.hp2 HG00423.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+13761_-47+1376 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204234 | |||||
| chr4:105204234
|
T | TACACAC | 13 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(10): Show | 13 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+13759_-47+1376 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204234 | |||||
| chr4:105204234
|
TACAC | T | 12 | a0001c0001t0001g0284a0001c0001t0038g0027a0002c0002t0037g0148others(9): Show | 12 | HG01516.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+13761_-47+1376 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204234 | |||||
| chr4:105204256
|
CACACACA others(7): Show |
C | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47+13755_-47+1376 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204256 | |||||
| chr4:105204256
|
CACACACA others(11): Show |
C | 1 | a0003c0008t0007g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-47+13755_-47+1377 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204256 | |||||
| chr4:105204258
|
CACACACA others(9): Show |
C | 5 | a0003c0008t0019g0330a0003c0008t0019g0333a0003c0008t0059g0324others(2): Show | 5 | HG02572.hp2 HG06807.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+13757_-47+1377 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204258 | |||||
| chr4:105204262
|
CACACACA others(5): Show |
C | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+13761_-47+1377 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204262 | |||||
| chr4:105204266
|
C | CACACACA others(11): Show |
2 | a0006c0006t0028g0004a0006c0006t0028g0006 | 2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47+13764_-47+1376 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204266 | |||||
| chr4:105204266
|
CACAT | C | 14 | a0001c0001t0004g0186a0003c0004t0016g0072a0003c0004t0016g0073others(11): Show | 14 | HG00741.hp2 HG01243.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-47+13774_-47+1377 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204266 | |||||
| chr4:105204268
|
CAT | C | 9 | a0001c0001t0001g0266a0001c0001t0005g0196a0001c0001t0006g0263others(6): Show | 9 | HG00741.hp1 HG01169.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+13765_-47+1376 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204268 | |||||
| chr4:105204268
|
CATACAT | C | 22 | a0003c0004t0016g0222a0003c0004t0016g0223a0003c0004t0017g0227others(19): Show | 22 | HG01109.hp1 HG01192.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-47+13765_-47+1377 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204268 | |||||
| chr4:105204270
|
T | C | 46 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0005g0187others(43): Show | 46 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+13765T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204270 | ||||||
| chr4:105204274
|
T | C | 15 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0018g0014others(12): Show | 15 | HG01243.hp2 HG02257.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47+13769T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204274 | ||||||
| chr4:105204278
|
T | C | 2 | a0003c0004t0035g0119a0003c0004t0105g0050 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-47+13773T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204278 | ||||||
| chr4:105204407
|
A | G | 1 | a0003c0004t0103g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-47+13902A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204407 | ||||||
| chr4:105204513
|
T | G | 6 | a0003c0008t0007g0046a0003c0008t0019g0330a0003c0008t0019g0333others(3): Show | 6 | HG01175.hp1 HG02572.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+14008T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204513 | ||||||
| chr4:105204558
|
G | A | 45 | a0001c0001t0013g0331a0004c0003t0002g0026a0004c0003t0002g0076others(42): Show | 45 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-47+14053G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204558 | ||||||
| chr4:105204594
|
A | G | 1 | a0002c0002t0026g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-47+14089A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204594 | ||||||
| chr4:105204667
|
G | T | 1 | a0001c0001t0004g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-47+14162G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204667 | ||||||
| chr4:105205003
|
G | A | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+14498G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205003 | ||||||
| chr4:105205240
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+14735A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205240 | ||||||
| chr4:105205256
|
G | C | 268 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0237others(265): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.-47+14751G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205256 | ||||||
| chr4:105205279
|
G | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+14774G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205279 | ||||||
| chr4:105205507
|
T | TC | 58 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(55): Show | 58 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.-47+15009dupC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105205507 | |||||
| chr4:105205638
|
A | C | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+15133A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205638 | ||||||
| chr4:105205693
|
A | T | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-47+15188A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205693 | ||||||
| chr4:105205785
|
C | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+15280C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205785 | ||||||
| chr4:105205806
|
C | G | 49 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(46): Show | 49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-47+15301C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205806 | ||||||
| chr4:105205847
|
C | T | 241 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0237others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.-47+15342C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205847 | ||||||
| chr4:105205854
|
A | G | 50 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(47): Show | 50 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47+15349A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205854 | ||||||
| chr4:105205964
|
C | A | 1 | a0020c0026t0009g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-47+15459C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205964 | ||||||
| chr4:105205964
|
C | T | 82 | a0001c0001t0001g0237a0001c0001t0003g0159a0001c0001t0009g0129others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-47+15459C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205964 | ||||||
| chr4:105206387
|
G | A | 3 | a0003c0004t0004g0033a0003c0004t0021g0034a0003c0031t0091g0019 | 3 | HG01891.hp1 HG03579.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-47+15882G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206387 | ||||||
| chr4:105206488
|
T | C | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+15983T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206488 | ||||||
| chr4:105206489
|
T | C | 50 | a0001c0001t0108g0002a0003c0004t0004g0033a0003c0004t0016g0072others(47): Show | 50 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47+15984T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206489 | ||||||
| chr4:105206491
|
G | C | 4 | a0001c0001t0108g0002a0003c0031t0091g0019a0013c0016t0001g0017others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+15986G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206491 | ||||||
| chr4:105206617
|
G | A | 1 | a0001c0001t0005g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-47+16112G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206617 | ||||||
| chr4:105206777
|
A | G | 1 | a0003c0004t0058g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+16272A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206777 | ||||||
| chr4:105206946
|
C | T | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+16441C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206946 | ||||||
| chr4:105206951
|
G | A | 69 | a0002c0002t0001g0130a0002c0002t0003g0124a0002c0002t0003g0125others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-47+16446G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206951 | ||||||
| chr4:105206952
|
A | G | 1 | a0001c0001t0034g0197 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-47+16447A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206952 | ||||||
| chr4:105207034
|
G | T | 42 | a0001c0001t0013g0331a0004c0003t0002g0026a0004c0003t0002g0076others(39): Show | 42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-47+16529G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207034 | ||||||
| chr4:105207035
|
A | C | 42 | a0001c0001t0013g0331a0004c0003t0002g0026a0004c0003t0002g0076others(39): Show | 42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-47+16530A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207035 | ||||||
| chr4:105207037
|
G | A | 42 | a0001c0001t0013g0331a0004c0003t0002g0026a0004c0003t0002g0076others(39): Show | 42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-47+16532G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207037 | ||||||
| chr4:105207207
|
A | G | 1 | a0004c0003t0097g0109 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-47+16702A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207207 | ||||||
| chr4:105207249
|
T | C | 3 | a0003c0031t0091g0019a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+16744T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207249 | ||||||
| chr4:105207305
|
A | G | 17 | a0003c0004t0030g0202a0003c0004t0058g0313a0003c0004t0083g0047others(14): Show | 17 | HG01175.hp1 HG02572.hp2 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+16800A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207305 | ||||||
| chr4:105207499
|
A | G | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+16994A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207499 | ||||||
| chr4:105207531
|
G | T | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-47+17026G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207531 | ||||||
| chr4:105207603
|
G | A | 240 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0003g0159others(237): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-47+17098G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207603 | ||||||
| chr4:105207720
|
C | T | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+17215C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207720 | ||||||
| chr4:105207797
|
C | T | 148 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0003g0159others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-47+17292C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207797 | ||||||
| chr4:105207918
|
A | G | 1 | a0003c0004t0004g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-47+17413A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207918 | ||||||
| chr4:105208177
|
T | TTCATTCT others(323): Show |
1 | a0005c0005t0005g0030 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-47+17683_-47+1768 others(334): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105208177 | |||||
| chr4:105208405
|
C | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47+17900C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105208405 | ||||||
| chr4:105208416
|
A | G | 3 | a0002c0002t0009g0174a0002c0002t0023g0122a0002c0002t0023g0123 | 3 | HG04184.hp2 HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-47+17911A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105208416 | ||||||
| chr4:105208441
|
A | G | 1 | a0001c0001t0008g0293 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-47+17936A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105208441 | ||||||
| chr4:105208721
|
A | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+18216A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105208721 | ||||||
| chr4:105209049
|
G | GTA | 50 | a0001c0001t0001g0235a0001c0001t0001g0240a0001c0001t0001g0258others(47): Show | 50 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-47+18592_-47+1859 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
G | GTATA | 34 | a0001c0001t0001g0233a0001c0001t0001g0257a0001c0001t0001g0332others(31): Show | 34 | HG00280.hp1 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-47+18590_-47+1859 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
G | GTATATA | 39 | a0001c0001t0001g0111a0001c0001t0001g0219a0001c0001t0001g0232others(36): Show | 39 | HG00280.hp2 HG00544.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47+18588_-47+1859 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
G | GTATATAT others(1): Show |
34 | a0001c0001t0001g0251a0001c0001t0001g0274a0001c0001t0001g0286others(31): Show | 34 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.-47+18586_-47+1859 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
G | GTATATAT others(3): Show |
19 | a0001c0001t0001g0250a0001c0001t0001g0260a0001c0001t0001g0287others(16): Show | 19 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-47+18584_-47+1859 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
G | GTATATAT others(5): Show |
9 | a0001c0001t0001g0268a0001c0001t0005g0191a0001c0001t0014g0216others(6): Show | 9 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+18582_-47+1859 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
G | GTATATAT others(7): Show |
2 | a0004c0003t0002g0088a0004c0003t0002g0099 | 2 | HG01943.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-47+18580_-47+1859 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTA | G | 9 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(6): Show | 9 | HG01517.hp2 HG02155.hp1 NA18998.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+18592_-47+1859 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATA | G | 11 | a0001c0001t0001g0297a0001c0001t0002g0253a0001c0001t0004g0186others(8): Show | 11 | HG00741.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47+18590_-47+1859 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATA | G | 13 | a0001c0001t0001g0241a0001c0001t0001g0321a0001c0001t0004g0246others(10): Show | 13 | HG01070.hp1 HG01255.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+18588_-47+1859 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(1): Show |
G | 4 | a0001c0001t0008g0199a0001c0001t0108g0002a0006c0006t0024g0342others(1): Show | 4 | HG01884.hp1 HG02602.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+18586_-47+1859 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(3): Show |
G | 8 | a0001c0001t0001g0189a0001c0001t0001g0237a0001c0001t0001g0289others(5): Show | 8 | HG01256.hp2 HG01346.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+18584_-47+1859 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(5): Show |
G | 9 | a0001c0001t0015g0269a0001c0001t0022g0238a0001c0001t0038g0027others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+18582_-47+1859 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(7): Show |
G | 1 | a0011c0015t0046g0347 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-47+18580_-47+1859 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(9): Show |
G | 4 | a0004c0003t0013g0086a0005c0005t0005g0294a0005c0005t0005g0295others(1): Show | 4 | HG02155.hp2 NA18747.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+18578_-47+1859 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(11): Show |
G | 4 | a0001c0007t0032g0116a0002c0002t0003g0133a0002c0002t0003g0231others(1): Show | 4 | HG00735.hp2 HG01169.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+18576_-47+1859 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(13): Show |
G | 15 | a0001c0001t0070g0032a0001c0007t0032g0340a0001c0007t0033g0036others(12): Show | 15 | HG00735.hp1 HG01109.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47+18574_-47+1859 others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(15): Show |
G | 23 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-47+18572_-47+1859 others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(17): Show |
G | 16 | a0003c0004t0058g0313a0003c0004t0083g0047a0003c0004t0105g0050others(13): Show | 16 | HG01175.hp1 HG02572.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+18570_-47+1859 others(28): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(19): Show |
G | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+18568_-47+1859 others(30): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(23): Show |
G | 5 | a0001c0001t0008g0301a0001c0001t0008g0302a0001c0001t0008g0303others(2): Show | 5 | NA18960.hp1 NA18979.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+18564_-47+1859 others(34): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209049
|
GTATATAT others(25): Show |
G | 1 | a0001c0001t0074g0021 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-47+18562_-47+1859 others(36): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | |||||
| chr4:105209051
|
A | G | 1 | a0002c0002t0027g0169 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-47+18546A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209051 | ||||||
| chr4:105209071
|
A | G | 6 | a0003c0004t0021g0120a0003c0004t0035g0062a0003c0004t0035g0119others(3): Show | 6 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+18566A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209071 | ||||||
| chr4:105209073
|
A | G | 22 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(19): Show | 22 | HG01192.hp2 HG01243.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-47+18568A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209073 | ||||||
| chr4:105209075
|
A | G | 16 | a0003c0004t0058g0313a0003c0004t0083g0047a0003c0004t0105g0050others(13): Show | 16 | HG01175.hp1 HG02572.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+18570A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209075 | ||||||
| chr4:105209077
|
A | G | 4 | a0003c0004t0004g0033a0003c0004t0021g0034a0012c0014t0060g0049others(1): Show | 4 | HG01891.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+18572A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209077 | ||||||
| chr4:105209099
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-47+18594G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209099 | ||||||
| chr4:105209120
|
A | G | 3 | a0003c0031t0091g0019a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+18615A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209120 | ||||||
| chr4:105209153
|
G | A | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47+18648G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209153 | ||||||
| chr4:105209511
|
A | C | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+19006A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209511 | ||||||
| chr4:105209641
|
G | GA | 49 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(46): Show | 49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-47+19136_-47+1913 others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209641 | ||||||
| chr4:105209664
|
T | C | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+19159T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209664 | ||||||
| chr4:105209868
|
G | A | 49 | a0001c0001t0013g0331a0004c0003t0002g0026a0004c0003t0002g0076others(46): Show | 49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-47+19363G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209868 | ||||||
| chr4:105209992
|
T | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | NA18998.hp2 NA19003.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+19487T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209992 | ||||||
| chr4:105210053
|
C | T | 124 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-47+19548C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105210053 | ||||||
| chr4:105210071
|
T | C | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+19566T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105210071 | ||||||
| chr4:105210269
|
A | C | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+19764A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105210269 | ||||||
| chr4:105210432
|
A | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0332 | 2 | NA18985.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-47+19927A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105210432 | ||||||
| chr4:105211088
|
T | G | 1 | a0004c0003t0002g0102 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-47+20583T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211088 | ||||||
| chr4:105211155
|
A | G | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+20650A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211155 | ||||||
| chr4:105211163
|
A | G | 61 | a0001c0001t0013g0331a0001c0001t0038g0027a0001c0001t0108g0002others(58): Show | 61 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-47+20658A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211163 | ||||||
| chr4:105211260
|
A | C | 2 | a0002c0002t0010g0149a0002c0002t0010g0170 | 2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-47+20755A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211260 | ||||||
| chr4:105211608
|
A | G | 14 | a0004c0003t0002g0076a0004c0003t0002g0077a0004c0003t0002g0079others(11): Show | 14 | HG00544.hp1 HG02015.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.-47+21103A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211608 | ||||||
| chr4:105211974
|
T | C | 1 | a0002c0002t0003g0244 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-47+21469T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211974 | ||||||
| chr4:105212027
|
C | T | 180 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.-47+21522C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212027 | ||||||
| chr4:105212314
|
G | A | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-21583G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212314 | ||||||
| chr4:105212593
|
G | T | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-21304G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212593 | ||||||
| chr4:105212676
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-21221A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212676 | ||||||
| chr4:105212761
|
G | A | 5 | a0002c0002t0003g0318a0002c0002t0009g0164a0002c0002t0023g0160others(2): Show | 5 | HG00609.hp1 HG01169.hp2 NA19072.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-21136G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212761 | ||||||
| chr4:105212817
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-46-21080C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212817 | ||||||
| chr4:105212860
|
C | T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-21037C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212860 | ||||||
| chr4:105213040
|
A | T | 1 | a0004c0003t0002g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-46-20857A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213040 | ||||||
| chr4:105213142
|
A | G | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-46-20755A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213142 | ||||||
| chr4:105213159
|
G | A | 72 | a0001c0001t0003g0159a0001c0001t0009g0129a0001c0001t0009g0151others(69): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-46-20738G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213159 | ||||||
| chr4:105213219
|
A | G | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-46-20678A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213219 | ||||||
| chr4:105213328
|
A | G | 1 | a0001c0001t0008g0303 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-46-20569A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213328 | ||||||
| chr4:105213500
|
G | T | 1 | a0002c0002t0003g0168 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-46-20397G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213500 | ||||||
| chr4:105213732
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-20165A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213732 | ||||||
| chr4:105213785
|
A | G | 49 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(46): Show | 49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-20112A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213785 | ||||||
| chr4:105213870
|
G | GT | 7 | a0002c0002t0003g0126a0002c0002t0003g0175a0002c0002t0003g0176others(4): Show | 7 | HG00544.hp2 NA18959.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-20020dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105213870 | |||||
| chr4:105214058
|
C | T | 1 | a0003c0019t0079g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-46-19839C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214058 | ||||||
| chr4:105214112
|
A | C | 3 | a0003c0031t0091g0019a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-19785A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214112 | ||||||
| chr4:105214159
|
G | T | 73 | a0001c0001t0003g0159a0001c0001t0009g0129a0001c0001t0009g0151others(70): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-46-19738G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214159 | ||||||
| chr4:105214172
|
G | A | 26 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(23): Show | 26 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46-19725G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214172 | ||||||
| chr4:105214291
|
C | T | 1 | a0001c0001t0005g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-46-19606C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214291 | ||||||
| chr4:105214301
|
A | AT | 25 | a0001c0001t0001g0260a0001c0001t0001g0274a0001c0001t0001g0284others(22): Show | 25 | HG00323.hp1 HG00738.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-46-19573dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | |||||
| chr4:105214301
|
A | ATT | 82 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.-46-19574_-46-1957 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | |||||
| chr4:105214301
|
A | ATTT | 68 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(65): Show | 68 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-46-19575_-46-1957 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | |||||
| chr4:105214301
|
A | ATTTT | 7 | a0001c0001t0092g0179a0001c0007t0090g0115a0004c0003t0002g0090others(4): Show | 7 | HG02145.hp1 HG02922.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-19576_-46-1957 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | |||||
| chr4:105214301
|
A | ATTTTT | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-19577_-46-1957 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | |||||
| chr4:105214301
|
AT | A | 37 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(34): Show | 37 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-46-19573delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | |||||
| chr4:105214301
|
ATTTTTTT | A | 28 | a0002c0002t0003g0124a0002c0002t0003g0125a0002c0002t0003g0126others(25): Show | 28 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-46-19579_-46-1957 others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | |||||
| chr4:105214471
|
A | AT | 78 | a0001c0001t0001g0111a0001c0001t0001g0241a0001c0001t0001g0260others(75): Show | 78 | HG00423.hp1 HG00673.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.-46-19403dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214471 | |||||
| chr4:105214471
|
A | ATT | 7 | a0001c0001t0001g0240a0002c0002t0025g0147a0003c0031t0091g0019others(4): Show | 7 | HG01192.hp1 HG02572.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-19404_-46-1940 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214471 | |||||
| chr4:105214499
|
A | AGAG | 49 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(46): Show | 49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-19396_-46-1939 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214499 | |||||
| chr4:105214926
|
T | C | 1 | a0003c0019t0079g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-46-18971T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214926 | ||||||
| chr4:105215376
|
T | A | 1 | a0001c0001t0070g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-46-18521T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215376 | ||||||
| chr4:105215803
|
A | G | 5 | a0006c0006t0024g0336a0006c0006t0036g0334a0006c0006t0036g0337others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-18094A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215803 | ||||||
| chr4:105215876
|
G | A | 120 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0003g0159others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-46-18021G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215876 | ||||||
| chr4:105215939
|
G | C | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-17958G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215939 | ||||||
| chr4:105215959
|
A | G | 6 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0297others(3): Show | 6 | HG01255.hp2 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-17938A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215959 | ||||||
| chr4:105216286
|
G | C | 2 | a0002c0002t0025g0131a0002c0002t0025g0147 | 2 | HG00738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-46-17611G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216286 | ||||||
| chr4:105216288
|
G | C | 1 | a0001c0001t0070g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-46-17609G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216288 | ||||||
| chr4:105216602
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-17295T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216602 | ||||||
| chr4:105216647
|
G | A | 1 | a0001c0001t0004g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-46-17250G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216647 | ||||||
| chr4:105216672
|
A | G | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-46-17225A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216672 | ||||||
| chr4:105216700
|
G | A | 1 | a0006c0006t0048g0003 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-46-17197G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216700 | ||||||
| chr4:105216801
|
G | C | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-17096G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216801 | ||||||
| chr4:105216980
|
G | A | 1 | a0001c0001t0008g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-46-16917G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216980 | ||||||
| chr4:105216989
|
T | C | 126 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-46-16908T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216989 | ||||||
| chr4:105217205
|
A | C | 26 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(23): Show | 26 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46-16692A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217205 | ||||||
| chr4:105217250
|
G | A | 1 | a0004c0003t0011g0103 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-46-16647G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217250 | ||||||
| chr4:105217310
|
T | G | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-16587T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217310 | ||||||
| chr4:105217634
|
A | G | 2 | a0001c0007t0032g0116a0001c0007t0090g0115 | 2 | HG00735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-46-16263A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217634 | ||||||
| chr4:105217700
|
T | C | 49 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(46): Show | 49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-16197T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217700 | ||||||
| chr4:105217736
|
G | A | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-16161G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217736 | ||||||
| chr4:105217765
|
A | G | 1 | a0003c0004t0021g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-46-16132A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217765 | ||||||
| chr4:105217841
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-16056C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217841 | ||||||
| chr4:105217919
|
A | G | 3 | a0003c0031t0091g0019a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15978A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217919 | ||||||
| chr4:105217960
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15937A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217960 | ||||||
| chr4:105217962
|
C | T | 1 | a0001c0001t0004g0262 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-46-15935C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217962 | ||||||
| chr4:105217992
|
C | G | 3 | a0003c0031t0091g0019a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15905C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217992 | ||||||
| chr4:105218230
|
T | C | 20 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-46-15667T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218230 | ||||||
| chr4:105218388
|
T | C | 1 | a0001c0001t0008g0301 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-46-15509T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218388 | ||||||
| chr4:105218428
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-46-15469G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218428 | ||||||
| chr4:105218466
|
A | C | 1 | a0001c0001t0007g0305 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-46-15431A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218466 | ||||||
| chr4:105218526
|
C | A | 1 | a0003c0004t0100g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-46-15371C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218526 | ||||||
| chr4:105218567
|
G | A | 2 | a0002c0002t0003g0244a0002c0002t0003g0245 | 2 | NA19058.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-46-15330G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218567 | ||||||
| chr4:105218616
|
C | T | 9 | a0001c0001t0070g0032a0001c0007t0032g0116a0001c0007t0032g0340others(6): Show | 9 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-15281C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218616 | ||||||
| chr4:105218673
|
C | T | 2 | a0005c0005t0050g0054a0005c0005t0051g0053 | 2 | HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-46-15224C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218673 | ||||||
| chr4:105218711
|
G | A | 3 | a0003c0031t0091g0019a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15186G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218711 | ||||||
| chr4:105218717
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15180A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218717 | ||||||
| chr4:105218862
|
T | C | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15035T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218862 | ||||||
| chr4:105219161
|
T | C | 17 | a0003c0004t0030g0202a0003c0004t0058g0313a0003c0004t0083g0047others(14): Show | 17 | HG01175.hp1 HG02572.hp2 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-14736T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219161 | ||||||
| chr4:105219232
|
C | T | 1 | a0004c0003t0002g0314 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-46-14665C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219232 | ||||||
| chr4:105219344
|
G | T | 239 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0003g0159others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-46-14553G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219344 | ||||||
| chr4:105219363
|
G | A | 10 | a0001c0001t0070g0032a0001c0001t0108g0002a0001c0007t0032g0116others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46-14534G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219363 | ||||||
| chr4:105219412
|
T | C | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-46-14485T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219412 | ||||||
| chr4:105219700
|
A | G | 2 | a0002c0002t0003g0142a0002c0002t0003g0145 | 2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-46-14197A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219700 | ||||||
| chr4:105219985
|
G | A | 1 | a0003c0004t0016g0222 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-46-13912G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219985 | ||||||
| chr4:105219988
|
C | G | 2 | a0002c0002t0026g0173a0006c0006t0068g0013 | 2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-46-13909C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219988 | ||||||
| chr4:105220051
|
C | T | 2 | a0001c0001t0034g0060a0001c0001t0078g0061 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-46-13846C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220051 | ||||||
| chr4:105220087
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-13810A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220087 | ||||||
| chr4:105220102
|
C | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-13795C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220102 | ||||||
| chr4:105220108
|
C | G | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-13789C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220108 | ||||||
| chr4:105220170
|
C | T | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-46-13727C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220170 | ||||||
| chr4:105220182
|
A | C | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-13715A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220182 | ||||||
| chr4:105220288
|
A | G | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-13609A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220288 | ||||||
| chr4:105220372
|
G | A | 2 | a0002c0002t0027g0157a0002c0002t0027g0169 | 2 | NA18955.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-46-13525G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220372 | ||||||
| chr4:105220520
|
C | A | 49 | a0001c0001t0013g0331a0004c0003t0002g0026a0004c0003t0002g0076others(46): Show | 49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-46-13377C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220520 | ||||||
| chr4:105220579
|
G | A | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-13318G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220579 | ||||||
| chr4:105220649
|
A | T | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-13248A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220649 | ||||||
| chr4:105220758
|
T | C | 12 | a0003c0004t0017g0227a0003c0004t0017g0228a0003c0004t0017g0229others(9): Show | 12 | HG02071.hp2 NA18944.hp2 NA18960.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46-13139T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220758 | ||||||
| chr4:105220759
|
A | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-13138A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220759 | ||||||
| chr4:105220830
|
T | G | 1 | a0014c0017t0003g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-46-13067T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220830 | ||||||
| chr4:105220922
|
ACTT | A | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-12972_-46-1297 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105220922 | |||||
| chr4:105220954
|
T | G | 1 | a0001c0029t0004g0277 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-46-12943T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220954 | ||||||
| chr4:105221262
|
T | C | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-46-12635T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221262 | ||||||
| chr4:105221384
|
T | C | 3 | a0003c0031t0091g0019a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-12513T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221384 | ||||||
| chr4:105221709
|
A | C | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-12188A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221709 | ||||||
| chr4:105221739
|
G | A | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-46-12158G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221739 | ||||||
| chr4:105221803
|
C | T | 120 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0003g0159others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-46-12094C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221803 | ||||||
| chr4:105221821
|
G | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-12076G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221821 | ||||||
| chr4:105221863
|
C | T | 1 | a0006c0006t0065g0341 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-46-12034C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221863 | ||||||
| chr4:105221865
|
T | TC | 10 | a0001c0001t0001g0240a0001c0001t0002g0254a0001c0001t0008g0302others(7): Show | 10 | HG01192.hp2 HG01256.hp2 HG03942.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46-12026dupC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105221865 | |||||
| chr4:105221866
|
C | CT | 6 | a0001c0001t0004g0311a0001c0001t0005g0190a0002c0002t0003g0128others(3): Show | 6 | HG00140.hp2 HG01978.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-12031_-46-1203 others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221866 | ||||||
| chr4:105221888
|
C | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-46-12009C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221888 | ||||||
| chr4:105221935
|
A | G | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-11962A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221935 | ||||||
| chr4:105221943
|
C | G | 49 | a0001c0001t0013g0331a0004c0003t0002g0026a0004c0003t0002g0076others(46): Show | 49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-46-11954C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221943 | ||||||
| chr4:105221983
|
T | C | 242 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(239): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-46-11914T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221983 | ||||||
| chr4:105222163
|
C | T | 1 | a0001c0001t0007g0306 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-46-11734C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222163 | ||||||
| chr4:105222164
|
G | A | 1 | a0003c0004t0030g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-46-11733G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222164 | ||||||
| chr4:105222177
|
G | A | 3 | a0001c0007t0032g0116a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG00735.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-11720G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222177 | ||||||
| chr4:105222225
|
A | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-11672A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222225 | ||||||
| chr4:105222285
|
G | A | 5 | a0003c0004t0030g0202a0003c0011t0007g0326a0003c0011t0042g0329others(2): Show | 5 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-11612G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222285 | ||||||
| chr4:105222285
|
G | T | 3 | a0001c0001t0006g0242a0001c0001t0080g0298a0017c0027t0022g0255 | 3 | HG00280.hp1 HG01496.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-46-11612G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222285 | ||||||
| chr4:105222318
|
T | G | 61 | a0001c0001t0013g0331a0001c0001t0038g0027a0001c0001t0108g0002others(58): Show | 61 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-46-11579T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222318 | ||||||
| chr4:105222335
|
C | T | 82 | a0001c0001t0001g0258a0001c0001t0003g0159a0001c0001t0009g0129others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-11562C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222335 | ||||||
| chr4:105222406
|
T | A | 1 | a0001c0001t0006g0265 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-46-11491T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222406 | ||||||
| chr4:105222541
|
C | T | 3 | a0006c0006t0036g0334a0006c0006t0081g0338a0006c0006t0082g0335 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-46-11356C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222541 | ||||||
| chr4:105222553
|
G | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-11344G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222553 | ||||||
| chr4:105222559
|
A | G | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-11338A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222559 | ||||||
| chr4:105222562
|
G | A | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46-11335G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222562 | ||||||
| chr4:105222640
|
G | A | 123 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0003g0159others(120): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-46-11257G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222640 | ||||||
| chr4:105222651
|
G | C | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-11246G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222651 | ||||||
| chr4:105222665
|
T | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-11232T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222665 | ||||||
| chr4:105222689
|
C | T | 8 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(5): Show | 8 | HG01192.hp1 HG02698.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46-11208C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222689 | ||||||
| chr4:105222743
|
G | T | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-11154G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222743 | ||||||
| chr4:105222754
|
C | T | 1 | a0005c0005t0005g0055 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-46-11143C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222754 | ||||||
| chr4:105222791
|
G | A | 177 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0003g0159others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.-46-11106G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222791 | ||||||
| chr4:105222808
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | NA18998.hp2 NA19003.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-46-11089G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222808 | ||||||
| chr4:105222809
|
G | A | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-11088G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222809 | ||||||
| chr4:105222811
|
G | A | 264 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0003g0159others(261): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-46-11086G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222811 | ||||||
| chr4:105222860
|
A | C | 3 | a0005c0005t0012g0069a0005c0005t0012g0070a0005c0005t0029g0068 | 3 | HG02970.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-11037A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222860 | ||||||
| chr4:105222987
|
T | G | 8 | a0001c0001t0001g0267a0006c0006t0028g0004a0006c0006t0028g0006others(5): Show | 8 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-10910T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222987 | ||||||
| chr4:105223130
|
T | A | 1 | a0001c0001t0001g0267 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-46-10767T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223130 | ||||||
| chr4:105223165
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-46-10732G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223165 | ||||||
| chr4:105223285
|
G | A | 48 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(45): Show | 48 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.-46-10612G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223285 | ||||||
| chr4:105223482
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-10415A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223482 | ||||||
| chr4:105223578
|
A | C | 183 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-46-10319A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223578 | ||||||
| chr4:105223635
|
T | C | 1 | a0003c0004t0035g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-10262T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223635 | ||||||
| chr4:105224006
|
C | T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-9891C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224006 | ||||||
| chr4:105224115
|
A | G | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-46-9782A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224115 | ||||||
| chr4:105224273
|
G | A | 52 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(49): Show | 52 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(49): Show |
intron_variant | MODIFIER | c.-46-9624G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224273 | ||||||
| chr4:105224311
|
A | G | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-9586A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224311 | ||||||
| chr4:105224471
|
C | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-9426C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224471 | ||||||
| chr4:105224535
|
T | G | 1 | a0002c0023t0003g0144 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-46-9362T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224535 | ||||||
| chr4:105224684
|
G | GTC | 62 | a0001c0001t0001g0111a0001c0001t0001g0235a0001c0001t0001g0237others(59): Show | 62 | HG00423.hp1 HG00673.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-46-9171_-46-9170d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTC | 53 | a0001c0001t0001g0241a0001c0001t0001g0258a0001c0001t0001g0259others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-46-9173_-46-9170d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTC | 30 | a0001c0001t0001g0233a0001c0001t0001g0256a0001c0001t0001g0257others(27): Show | 30 | HG00323.hp1 HG01192.hp2 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-46-9175_-46-9170d others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(1): Show |
28 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0312others(25): Show | 28 | HG00673.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46-9177_-46-9170d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(3): Show |
24 | a0001c0001t0001g0307a0001c0001t0002g0253a0001c0001t0003g0159others(21): Show | 24 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-46-9179_-46-9170d others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(5): Show |
18 | a0001c0001t0001g0192a0001c0001t0006g0204a0001c0001t0006g0207others(15): Show | 18 | HG00140.hp1 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-46-9181_-46-9170d others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(7): Show |
19 | a0001c0001t0004g0209a0001c0001t0005g0191a0001c0001t0006g0212others(16): Show | 19 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-46-9183_-46-9170d others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(9): Show |
10 | a0001c0001t0001g0189a0001c0001t0004g0203a0001c0001t0005g0187others(7): Show | 10 | HG00323.hp2 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46-9185_-46-9170d others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(11): Show |
3 | a0001c0001t0006g0214a0001c0001t0054g0188a0005c0005t0005g0059 | 3 | HG01358.hp1 HG02300.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-46-9187_-46-9170d others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(13): Show |
1 | a0001c0001t0056g0194 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-46-9189_-46-9170d others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(17): Show |
1 | a0001c0007t0071g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-46-9193_-46-9170d others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(19): Show |
1 | a0001c0007t0032g0340 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-46-9195_-46-9170d others(28): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(21): Show |
1 | a0003c0004t0105g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-9197_-46-9170d others(30): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
G | GTCTCTCT others(25): Show |
1 | a0003c0004t0083g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-46-9201_-46-9170d others(34): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
GTC | G | 24 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(21): Show | 24 | HG00280.hp1 HG01243.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.-46-9171_-46-9170d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
GTCTC | G | 3 | a0004c0003t0002g0092a0006c0006t0047g0121a0006c0006t0065g0341 | 3 | HG02886.hp2 HG02965.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-46-9173_-46-9170d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
GTCTCTC | G | 4 | a0004c0003t0002g0026a0004c0003t0002g0094a0004c0003t0002g0234others(1): Show | 4 | HG00423.hp2 NA18980.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-9175_-46-9170d others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
GTCTCTCT others(1): Show |
G | 31 | a0004c0003t0002g0076a0004c0003t0002g0077a0004c0003t0002g0079others(28): Show | 31 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-46-9177_-46-9170d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
GTCTCTCT others(3): Show |
G | 7 | a0001c0001t0007g0211a0001c0001t0108g0002a0004c0003t0021g0117others(4): Show | 7 | HG01070.hp1 HG01517.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-9179_-46-9170d others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
GTCTCTCT others(7): Show |
G | 1 | a0003c0004t0030g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-46-9183_-46-9170d others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
GTCTCTCT others(9): Show |
G | 7 | a0001c0001t0013g0331a0004c0003t0002g0088a0004c0003t0002g0110others(4): Show | 7 | HG01071.hp2 HG01074.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-9185_-46-9170d others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224684
|
GTCTCTCT others(11): Show |
G | 1 | a0004c0003t0013g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-46-9187_-46-9170d others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | |||||
| chr4:105224727
|
T | TCTCTCTC others(4): Show |
1 | a0001c0001t0004g0186 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-46-9170_-46-9169i others(13): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224727 | ||||||
| chr4:105224803
|
C | T | 1 | a0002c0002t0086g0166 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-46-9094C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224803 | ||||||
| chr4:105225092
|
T | G | 1 | a0001c0001t0054g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-46-8805T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225092 | ||||||
| chr4:105225106
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0297 | 2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-46-8791T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225106 | ||||||
| chr4:105225128
|
G | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-8769G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225128 | ||||||
| chr4:105225140
|
G | A | 1 | a0002c0002t0003g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-46-8757G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225140 | ||||||
| chr4:105225185
|
C | CGT | 7 | a0001c0001t0001g0257a0001c0001t0001g0284a0001c0001t0007g0292others(4): Show | 7 | HG02735.hp1 HG03239.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-8688_-46-8687d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(1): Show |
9 | a0001c0001t0034g0060a0001c0001t0038g0027a0001c0001t0078g0061others(6): Show | 9 | HG00609.hp1 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-8694_-46-8687d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(3): Show |
8 | a0001c0001t0001g0189a0001c0001t0108g0002a0002c0002t0003g0244others(5): Show | 8 | HG01261.hp2 HG01346.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46-8696_-46-8687d others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(5): Show |
54 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(51): Show | 54 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.-46-8698_-46-8687d others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(7): Show |
76 | a0001c0001t0001g0192a0001c0001t0001g0232a0001c0001t0003g0159others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-46-8700_-46-8687d others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(9): Show |
21 | a0001c0001t0034g0197a0001c0001t0056g0194a0002c0002t0025g0131others(18): Show | 21 | HG00642.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-46-8702_-46-8687d others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(11): Show |
15 | a0001c0001t0054g0188a0001c0001t0085g0029a0001c0001t0087g0028others(12): Show | 15 | HG01109.hp1 HG01361.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-46-8704_-46-8687d others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(13): Show |
7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01099.hp2 HG01192.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-8706_-46-8687d others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(15): Show |
4 | a0003c0004t0099g0064a0003c0004t0102g0065a0006c0006t0047g0121others(1): Show | 4 | HG01192.hp2 HG02602.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-8708_-46-8687d others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
C | CGTGTGTG others(17): Show |
2 | a0003c0004t0016g0223a0003c0004t0101g0066 | 2 | HG02145.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-46-8710_-46-8687d others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225185
|
CGTGTGT | C | 43 | a0001c0001t0013g0331a0004c0003t0002g0026a0004c0003t0002g0076others(40): Show | 43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-46-8692_-46-8687d others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | |||||
| chr4:105225320
|
A | C | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-8577A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225320 | ||||||
| chr4:105225345
|
C | T | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-8552C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225345 | ||||||
| chr4:105225365
|
C | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-8532C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225365 | ||||||
| chr4:105225662
|
A | G | 2 | a0002c0002t0026g0173a0006c0006t0068g0013 | 2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-46-8235A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225662 | ||||||
| chr4:105225878
|
T | C | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46-8019T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225878 | ||||||
| chr4:105225909
|
G | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-7988G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225909 | ||||||
| chr4:105225978
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-7919A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225978 | ||||||
| chr4:105226064
|
C | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-7833C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226064 | ||||||
| chr4:105226077
|
C | CT | 268 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(265): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.-46-7818dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105226077 | |||||
| chr4:105226099
|
TA | T | 23 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(20): Show | 23 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-46-7789delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105226099 | |||||
| chr4:105226416
|
G | T | 1 | a0002c0002t0003g0316 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-46-7481G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226416 | ||||||
| chr4:105226633
|
CCCTCCCT others(3): Show |
C | 1 | a0001c0001t0014g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-46-7249_-46-7240d others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105226633 | |||||
| chr4:105226721
|
A | G | 1 | a0005c0005t0050g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-46-7176A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226721 | ||||||
| chr4:105226756
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-7141A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226756 | ||||||
| chr4:105226762
|
T | A | 49 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(46): Show | 49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-7135T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226762 | ||||||
| chr4:105226787
|
C | G | 3 | a0003c0031t0091g0019a0013c0016t0001g0017a0013c0016t0001g0018 | 3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-7110C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226787 | ||||||
| chr4:105226841
|
T | C | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-46-7056T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226841 | ||||||
| chr4:105226922
|
C | T | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-6975C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226922 | ||||||
| chr4:105226979
|
T | G | 49 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(46): Show | 49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-6918T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226979 | ||||||
| chr4:105226993
|
A | G | 1 | a0004c0003t0021g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-46-6904A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226993 | ||||||
| chr4:105227056
|
C | T | 3 | a0002c0002t0009g0174a0002c0002t0023g0122a0002c0002t0023g0123 | 3 | HG04184.hp2 HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-46-6841C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227056 | ||||||
| chr4:105227058
|
G | A | 1 | a0001c0001t0080g0298 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-46-6839G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227058 | ||||||
| chr4:105227065
|
A | G | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG01243.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-46-6832A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227065 | ||||||
| chr4:105227066
|
G | C | 1 | a0003c0004t0016g0223 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-46-6831G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227066 | ||||||
| chr4:105227121
|
C | A | 4 | a0008c0010t0011g0007a0008c0010t0011g0008a0008c0010t0011g0010others(1): Show | 4 | HG02145.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-6776C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227121 | ||||||
| chr4:105227489
|
G | A | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-6408G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227489 | ||||||
| chr4:105227492
|
TAGACCTT others(93): Show |
T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-6403_-46-6304d others(102): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105227492 | |||||
| chr4:105227596
|
A | T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-6301A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227596 | ||||||
| chr4:105227598
|
A | T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-6299A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227598 | ||||||
| chr4:105227599
|
AGG | A | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-6297_-46-6296d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227599 | ||||||
| chr4:105227601
|
G | C | 126 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-46-6296G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227601 | ||||||
| chr4:105227765
|
A | G | 1 | a0003c0004t0016g0222 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-46-6132A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227765 | ||||||
| chr4:105227849
|
G | C | 27 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(24): Show | 27 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-6048G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227849 | ||||||
| chr4:105228157
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-5740A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228157 | ||||||
| chr4:105228191
|
T | C | 1 | a0003c0008t0067g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-46-5706T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228191 | ||||||
| chr4:105228558
|
C | T | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-5339C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228558 | ||||||
| chr4:105228573
|
A | G | 1 | a0003c0004t0105g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-5324A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228573 | ||||||
| chr4:105228679
|
T | C | 1 | a0001c0001t0007g0306 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-46-5218T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228679 | ||||||
| chr4:105229011
|
T | C | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-4886T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229011 | ||||||
| chr4:105229076
|
A | C | 47 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(44): Show | 47 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.-46-4821A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229076 | ||||||
| chr4:105229295
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-4602T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229295 | ||||||
| chr4:105229304
|
A | G | 1 | a0009c0013t0001g0322 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-46-4593A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229304 | ||||||
| chr4:105229398
|
C | T | 25 | a0004c0003t0013g0086a0005c0005t0005g0030a0005c0005t0005g0040others(22): Show | 25 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.-46-4499C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229398 | ||||||
| chr4:105229502
|
T | G | 49 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(46): Show | 49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-4395T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229502 | ||||||
| chr4:105229503
|
G | T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-4394G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229503 | ||||||
| chr4:105229516
|
GGC | G | 4 | a0001c0001t0006g0263a0001c0001t0006g0264a0001c0001t0006g0265others(1): Show | 4 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-4380_-46-4379d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229516 | ||||||
| chr4:105229652
|
TA | T | 14 | a0001c0001t0014g0210a0001c0007t0032g0116a0001c0007t0032g0340others(11): Show | 14 | HG00735.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.-46-4231delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105229652 | |||||
| chr4:105230053
|
A | T | 8 | a0001c0001t0015g0269a0006c0006t0028g0004a0006c0006t0028g0006others(5): Show | 8 | HG01192.hp1 HG02818.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-3844A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230053 | ||||||
| chr4:105230055
|
T | A | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-3842T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230055 | ||||||
| chr4:105230408
|
T | C | 44 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(41): Show | 44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.-46-3489T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230408 | ||||||
| chr4:105230485
|
G | A | 125 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-46-3412G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230485 | ||||||
| chr4:105230624
|
A | G | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-3273A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230624 | ||||||
| chr4:105230686
|
T | C | 244 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-46-3211T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230686 | ||||||
| chr4:105230760
|
C | T | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-3137C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230760 | ||||||
| chr4:105230800
|
T | C | 1 | a0001c0001t0022g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-46-3097T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230800 | ||||||
| chr4:105230805
|
T | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-3092T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230805 | ||||||
| chr4:105230880
|
G | A | 24 | a0005c0005t0005g0030a0005c0005t0005g0040a0005c0005t0005g0041others(21): Show | 24 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-46-3017G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230880 | ||||||
| chr4:105230954
|
T | G | 77 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.-46-2943T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230954 | ||||||
| chr4:105231619
|
C | T | 1 | a0002c0002t0020g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-46-2278C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231619 | ||||||
| chr4:105231667
|
A | G | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-2230A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231667 | ||||||
| chr4:105231720
|
C | A | 108 | a0001c0001t0001g0237a0001c0001t0003g0159a0001c0001t0004g0203others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-46-2177C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231720 | ||||||
| chr4:105231809
|
T | C | 3 | a0005c0005t0012g0069a0005c0005t0012g0070a0005c0005t0029g0068 | 3 | HG02970.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-2088T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231809 | ||||||
| chr4:105231827
|
T | C | 119 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(116): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-46-2070T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231827 | ||||||
| chr4:105231828
|
G | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-2069G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231828 | ||||||
| chr4:105231897
|
A | G | 4 | a0001c0001t0034g0060a0001c0001t0078g0061a0003c0004t0004g0033others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-2000A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231897 | ||||||
| chr4:105231901
|
G | T | 1 | a0002c0002t0023g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-46-1996G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231901 | ||||||
| chr4:105232001
|
T | C | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | NA18998.hp2 NA19003.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-1896T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232001 | ||||||
| chr4:105232022
|
C | G | 1 | a0002c0002t0003g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-46-1875C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232022 | ||||||
| chr4:105232063
|
C | A | 1 | a0001c0001t0005g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-46-1834C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232063 | ||||||
| chr4:105232395
|
G | A | 2 | a0006c0006t0028g0009a0006c0006t0106g0001 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-46-1502G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232395 | ||||||
| chr4:105232399
|
G | A | 1 | a0004c0003t0002g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-46-1498G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232399 | ||||||
| chr4:105232440
|
C | G | 1 | a0004c0003t0002g0101 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-46-1457C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232440 | ||||||
| chr4:105232546
|
A | C | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-1351A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232546 | ||||||
| chr4:105232714
|
A | G | 1 | a0003c0004t0083g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-46-1183A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232714 | ||||||
| chr4:105232969
|
G | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-928G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232969 | ||||||
| chr4:105233034
|
C | A | 1 | a0001c0001t0008g0302 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-46-863C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233034 | ||||||
| chr4:105233102
|
G | T | 1 | a0002c0002t0020g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-46-795G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233102 | ||||||
| chr4:105233255
|
G | A | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-642G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233255 | ||||||
| chr4:105233343
|
C | T | 59 | a0001c0001t0038g0027a0004c0003t0002g0026a0004c0003t0002g0076others(56): Show | 59 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-46-554C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233343 | ||||||
| chr4:105233344
|
G | A | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-46-553G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233344 | ||||||
| chr4:105233356
|
C | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-541C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233356 | ||||||
| chr4:105233378
|
C | T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-519C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233378 | ||||||
| chr4:105233383
|
C | CAAAAAAA others(2): Show |
9 | a0001c0001t0092g0179a0002c0002t0003g0126a0002c0002t0086g0166others(6): Show | 9 | HG01169.hp2 HG02080.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-504_-46-496dup others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233383
|
C | CAAAAAAA others(3): Show |
120 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(117): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-46-505_-46-496dup others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233383
|
C | CAAAAAAA others(4): Show |
34 | a0001c0001t0006g0207a0001c0001t0006g0212a0001c0001t0014g0215others(31): Show | 34 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-46-506_-46-496dup others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233383
|
C | CAAAAAAA others(5): Show |
9 | a0001c0001t0009g0129a0001c0001t0009g0151a0001c0001t0094g0140others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-507_-46-496dup others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233383
|
C | CAAAAAAA others(6): Show |
12 | a0001c0001t0003g0159a0003c0004t0058g0313a0003c0004t0083g0047others(9): Show | 12 | HG02723.hp2 HG02809.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.-46-508_-46-496dup others(13): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233383
|
C | CAAAAAAA others(7): Show |
20 | a0003c0004t0016g0072a0003c0004t0016g0222a0003c0004t0016g0223others(17): Show | 20 | HG01109.hp1 HG01175.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.-46-509_-46-496dup others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233383
|
C | CAAAAAAA others(8): Show |
11 | a0003c0004t0016g0073a0003c0004t0017g0227a0003c0004t0017g0229others(8): Show | 11 | HG01099.hp2 HG01192.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-46-510_-46-496dup others(15): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233383
|
C | CAAAAAAA others(9): Show |
3 | a0003c0004t0018g0224a0003c0004t0100g0042a0003c0004t0102g0065 | 3 | HG02257.hp2 HG02647.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-46-511_-46-496dup others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233383
|
CA | C | 40 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0290others(37): Show | 40 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-46-496delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | |||||
| chr4:105233542
|
G | A | 1 | a0004c0003t0002g0079 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-46-355G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233542 | ||||||
| chr4:105233790
|
C | T | 1 | a0003c0004t0105g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-107C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233790 | ||||||
| chr4:105233833
|
T | TATAG | 101 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(98): Show | 101 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-46-42_-46-39dupTA others(2): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233833 | |||||
| chr4:105233833
|
T | TATAGATA others(1): Show |
5 | a0003c0004t0105g0050a0003c0019t0079g0043a0003c0031t0091g0019others(2): Show | 5 | HG01099.hp2 HG02602.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-46_-46-39dupTA others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233833 | |||||
| chr4:105233833
|
TATAGATA others(1): Show |
T | 109 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-46-46_-46-39delTA others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233833 | |||||
| chr4:105237369
|
A | G | 3 | a0003c0004t0099g0064a0003c0004t0101g0066a0003c0004t0102g0065 | 3 | HG01192.hp2 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3409+18A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237369 | ||||||
| chr4:105237581
|
G | A | 6 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(3): Show | 6 | HG01192.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3409+230G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237581 | ||||||
| chr4:105237663
|
T | A | 1 | a0003c0004t0102g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3409+312T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237663 | ||||||
| chr4:105237764
|
A | T | 1 | a0003c0004t0103g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3409+413A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237764 | ||||||
| chr4:105237842
|
G | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3409+491G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237842 | ||||||
| chr4:105237969
|
A | C | 1 | a0002c0002t0020g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3409+618A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237969 | ||||||
| chr4:105238107
|
C | T | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+756C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238107 | ||||||
| chr4:105238114
|
AGT | A | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.3409+767_3409+768d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105238114 | |||||
| chr4:105238229
|
G | A | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+878G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238229 | ||||||
| chr4:105238425
|
T | G | 4 | a0007c0009t0029g0057a0007c0009t0052g0031a0007c0009t0053g0056others(1): Show | 4 | HG00738.hp2 HG01891.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.3409+1074T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238425 | ||||||
| chr4:105238487
|
T | A | 347 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(344): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.3409+1136T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238487 | ||||||
| chr4:105238850
|
C | T | 1 | a0019c0024t0031g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3409+1499C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238850 | ||||||
| chr4:105238874
|
G | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3409+1523G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238874 | ||||||
| chr4:105238875
|
C | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3409+1524C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238875 | ||||||
| chr4:105238876
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3409+1525A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238876 | ||||||
| chr4:105238976
|
G | A | 40 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(37): Show | 40 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.3409+1625G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238976 | ||||||
| chr4:105239004
|
A | G | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+1653A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239004 | ||||||
| chr4:105239062
|
G | T | 1 | a0001c0001t0030g0280 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3409+1711G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239062 | ||||||
| chr4:105239067
|
G | T | 1 | a0001c0001t0007g0300 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3409+1716G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239067 | ||||||
| chr4:105239070
|
T | C | 1 | a0001c0001t0007g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3409+1719T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239070 | ||||||
| chr4:105239072
|
T | TTGTTTTT others(3): Show |
57 | a0001c0001t0001g0258a0001c0001t0108g0002a0004c0003t0002g0026others(54): Show | 57 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239072 | |||||
| chr4:105239074
|
G | GTTTTTTT others(2): Show |
36 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(33): Show | 36 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(13): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239074 | |||||
| chr4:105239074
|
G | GTTTTTTT others(3): Show |
63 | a0001c0001t0070g0032a0001c0001t0092g0179a0001c0007t0032g0116others(60): Show | 63 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(60): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239074 | |||||
| chr4:105239074
|
G | GTTTTTTT others(4): Show |
103 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(100): Show | 103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(15): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239074 | |||||
| chr4:105239074
|
G | GTTTTTTT others(5): Show |
4 | a0002c0002t0026g0137a0002c0002t0063g0012a0002c0002t0086g0166others(1): Show | 4 | HG01169.hp2 HG02056.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239074 | |||||
| chr4:105239082
|
T | G | 1 | a0006c0006t0047g0121 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3409+1731T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239082 | ||||||
| chr4:105239083
|
T | G | 4 | a0002c0002t0003g0135a0002c0002t0027g0157a0002c0002t0027g0169others(1): Show | 4 | HG03669.hp1 HG03688.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.3409+1732T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239083 | ||||||
| chr4:105239208
|
A | C | 111 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.3409+1857A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239208 | ||||||
| chr4:105239325
|
T | C | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3409+1974T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239325 | ||||||
| chr4:105239338
|
A | G | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+1987A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239338 | ||||||
| chr4:105239579
|
G | C | 3 | a0001c0001t0073g0025a0001c0001t0075g0024a0001c0001t0076g0023 | 3 | HG02004.hp2 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3410-1760G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239579 | ||||||
| chr4:105239658
|
G | A | 1 | a0009c0013t0001g0322 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3410-1681G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239658 | ||||||
| chr4:105239825
|
G | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3410-1514G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239825 | ||||||
| chr4:105239898
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3410-1441T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239898 | ||||||
| chr4:105240118
|
A | G | 10 | a0002c0002t0003g0124a0002c0002t0003g0125a0002c0002t0003g0126others(7): Show | 10 | HG00544.hp2 NA18959.hp2 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.3410-1221A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105240118 | ||||||
| chr4:105240309
|
C | T | 1 | a0012c0014t0060g0049 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3410-1030C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105240309 | ||||||
| chr4:105240470
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3410-869C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105240470 | ||||||
| chr4:105240915
|
G | A | 3 | a0001c0001t0001g0321a0001c0001t0004g0246a0001c0001t0008g0247 | 3 | HG01255.hp2 HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.3410-424G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105240915 | ||||||
| chr4:105241024
|
G | A | 1 | a0004c0003t0002g0101 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3410-315G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105241024 | ||||||
| chr4:105241058
|
GT | G | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3410-280delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105241058 | ||||||
| chr4:105241161
|
A | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3410-178A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105241161 | ||||||
| chr4:105241546
|
G | A | 1 | a0003c0004t0030g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3500+117G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105241546 | ||||||
| chr4:105241736
|
G | A | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3500+307G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105241736 | ||||||
| chr4:105241938
|
CT | C | 187 | a0001c0001t0001g0111a0001c0001t0001g0189a0001c0001t0001g0192others(184): Show | 187 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.3500+524delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr4 | 105241938 | |||||
| chr4:105241938
|
CTT | C | 55 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(52): Show | 55 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.3500+523_3500+524d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr4 | 105241938 | |||||
| chr4:105241952
|
TTC | T | 95 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.3500+524_3500+525d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105241952 | ||||||
| chr4:105241953
|
TC | T | 9 | a0001c0001t0072g0022a0001c0001t0073g0025a0001c0001t0074g0021others(6): Show | 9 | HG00323.hp1 HG01081.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.3500+525delC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105241953 | ||||||
| chr4:105242182
|
T | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3501-652T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105242182 | ||||||
| chr4:105242432
|
A | T | 1 | a0001c0001t0004g0262 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3501-402A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105242432 | ||||||
| chr4:105242479
|
T | G | 1 | a0011c0015t0046g0347 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3501-355T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105242479 | ||||||
| chr4:105243040
|
C | T | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3594+113C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | chr4 | 105243040 | ||||||
| chr4:105243073
|
TAAG | T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3594+151_3594+153d others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr4 | 105243073 | |||||
| chr4:105243127
|
T | G | 75 | a0001c0001t0001g0232a0001c0001t0003g0159a0001c0001t0009g0129others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.3594+200T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | chr4 | 105243127 | ||||||
| chr4:105243484
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3595-86A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | chr4 | 105243484 | ||||||
| chr4:105243566
|
G | A | 7 | a0002c0002t0003g0318a0006c0006t0028g0004a0006c0006t0028g0006others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.3595-4G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | chr4 | 105243566 | ||||||
| chr4:105243823
|
G | A | 16 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.3803+45G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105243823 | ||||||
| chr4:105243834
|
T | C | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3803+56T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105243834 | ||||||
| chr4:105244056
|
T | C | 1 | a0001c0001t0005g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3803+278T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244056 | ||||||
| chr4:105244267
|
A | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+489A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244267 | ||||||
| chr4:105244351
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+573A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244351 | ||||||
| chr4:105244408
|
G | T | 1 | a0001c0001t0007g0306 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3803+630G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244408 | ||||||
| chr4:105244584
|
A | ATC | 6 | a0003c0004t0004g0033a0003c0004t0021g0034a0003c0004t0058g0313others(3): Show | 6 | HG01175.hp1 HG01891.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244584
|
A | ATCT | 7 | a0001c0007t0032g0340a0001c0007t0033g0114a0001c0007t0057g0038others(4): Show | 7 | HG02451.hp2 HG02809.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244584
|
A | ATCTT | 4 | a0001c0007t0032g0116a0001c0007t0033g0036a0001c0007t0071g0180others(1): Show | 4 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244584
|
A | ATCTTT | 3 | a0001c0001t0070g0032a0001c0001t0092g0179a0001c0001t0108g0002 | 3 | HG01884.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3803+807_3803+808i others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244584
|
A | ATCTTTTT | 5 | a0001c0001t0072g0022a0001c0001t0073g0025a0001c0001t0074g0021others(2): Show | 5 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244584
|
A | ATCTTTTT others(2): Show |
9 | a0001c0001t0006g0204a0001c0001t0006g0206a0001c0001t0006g0207others(6): Show | 9 | HG00323.hp2 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244584
|
A | ATCTTTTT others(3): Show |
7 | a0001c0001t0004g0203a0001c0001t0006g0214a0001c0001t0006g0319others(4): Show | 7 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244584
|
ATGTTTTT others(1): Show |
A | 63 | a0001c0001t0001g0232a0002c0002t0001g0130a0002c0002t0003g0124others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.3803+808_3803+815d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244584
|
ATGTTTTT others(5): Show |
A | 4 | a0002c0002t0003g0168a0002c0002t0003g0177a0002c0002t0020g0201others(1): Show | 4 | HG01358.hp2 HG01981.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3803+808_3803+819d others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | |||||
| chr4:105244585
|
T | TC | 10 | a0003c0004t0017g0320a0003c0004t0041g0074a0003c0004t0101g0066others(7): Show | 10 | HG01109.hp1 HG01192.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(3): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244585 | ||||||
| chr4:105244586
|
G | C | 38 | a0002c0002t0003g0243a0003c0004t0016g0072a0003c0004t0016g0073others(35): Show | 38 | HG01192.hp2 HG01243.hp2 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.3803+808G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244586 | ||||||
| chr4:105244586
|
G | GT | 60 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0240others(57): Show | 60 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.3803+834dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244586 | |||||
| chr4:105244586
|
G | GTT | 11 | a0001c0001t0001g0260a0001c0001t0004g0186a0001c0001t0005g0190others(8): Show | 11 | HG00738.hp2 HG00741.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.3803+833_3803+834d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244586 | |||||
| chr4:105244586
|
G | T | 52 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(49): Show | 52 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.3803+808G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244586 | ||||||
| chr4:105244586
|
GT | G | 6 | a0004c0003t0002g0118a0004c0003t0021g0117a0006c0006t0024g0342others(3): Show | 6 | HG01070.hp1 HG01074.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3803+834delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244586 | |||||
| chr4:105244587
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+809T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244587 | ||||||
| chr4:105244593
|
T | C | 5 | a0001c0001t0003g0159a0001c0001t0009g0129a0001c0001t0009g0151others(2): Show | 5 | HG02723.hp2 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3803+815T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244593 | ||||||
| chr4:105244594
|
T | C | 63 | a0001c0001t0001g0232a0002c0002t0001g0130a0002c0002t0003g0124others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.3803+816T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244594 | ||||||
| chr4:105244595
|
T | C | 1 | a0002c0002t0003g0244 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3803+817T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244595 | ||||||
| chr4:105244598
|
T | C | 4 | a0002c0002t0003g0168a0002c0002t0003g0177a0002c0002t0020g0201others(1): Show | 4 | HG01358.hp2 HG01981.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3803+820T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244598 | ||||||
| chr4:105244625
|
C | T | 1 | a0003c0008t0007g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3803+847C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244625 | ||||||
| chr4:105244656
|
C | T | 1 | a0001c0001t0072g0022 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3803+878C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244656 | ||||||
| chr4:105244672
|
C | T | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3803+894C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244672 | ||||||
| chr4:105244715
|
C | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3803+937C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244715 | ||||||
| chr4:105244879
|
C | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+1101C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244879 | ||||||
| chr4:105244881
|
C | T | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3803+1103C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244881 | ||||||
| chr4:105244916
|
C | T | 3 | a0003c0011t0042g0329a0003c0011t0049g0327a0003c0018t0019g0325 | 3 | HG02809.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3803+1138C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244916 | ||||||
| chr4:105244982
|
A | G | 8 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(5): Show | 8 | HG01192.hp1 HG02698.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3803+1204A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244982 | ||||||
| chr4:105245265
|
G | A | 1 | a0002c0002t0003g0177 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3803+1487G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245265 | ||||||
| chr4:105245302
|
T | C | 1 | a0001c0001t0008g0301 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3803+1524T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245302 | ||||||
| chr4:105245400
|
G | A | 1 | a0001c0001t0073g0025 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3803+1622G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245400 | ||||||
| chr4:105245566
|
G | T | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+1788G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245566 | ||||||
| chr4:105245813
|
C | G | 1 | a0006c0006t0024g0336 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3803+2035C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245813 | ||||||
| chr4:105245858
|
G | A | 1 | a0004c0003t0002g0112 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3803+2080G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245858 | ||||||
| chr4:105245984
|
C | T | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3803+2206C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245984 | ||||||
| chr4:105246023
|
C | T | 2 | a0002c0002t0003g0152a0002c0002t0003g0153 | 2 | NA18979.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.3803+2245C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246023 | ||||||
| chr4:105246275
|
T | TA | 229 | a0001c0001t0001g0219a0001c0001t0001g0232a0001c0001t0001g0233others(226): Show | 229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.3803+2503dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105246275 | |||||
| chr4:105246501
|
TAATGCTT others(4): Show |
T | 6 | a0003c0008t0007g0046a0003c0008t0019g0330a0003c0008t0019g0333others(3): Show | 6 | HG01175.hp1 HG02572.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.3803+2724_3803+273 others(15): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246501 | ||||||
| chr4:105246587
|
C | T | 107 | a0001c0001t0001g0237a0001c0001t0003g0159a0001c0001t0004g0203others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.3803+2809C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246587 | ||||||
| chr4:105246602
|
T | C | 2 | a0003c0004t0004g0033a0003c0004t0021g0034 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3803+2824T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246602 | ||||||
| chr4:105246710
|
A | T | 1 | a0001c0001t0001g0274 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3803+2932A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246710 | ||||||
| chr4:105246711
|
T | A | 1 | a0001c0001t0001g0274 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3803+2933T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246711 | ||||||
| chr4:105246712
|
A | T | 1 | a0001c0001t0001g0274 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3803+2934A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246712 | ||||||
| chr4:105246845
|
G | A | 2 | a0003c0004t0016g0072a0003c0004t0016g0073 | 2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3803+3067G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246845 | ||||||
| chr4:105247137
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3803+3359C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247137 | ||||||
| chr4:105247376
|
AAAAG | A | 58 | a0001c0001t0001g0274a0001c0001t0002g0254a0001c0001t0005g0270others(55): Show | 58 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.3803+3603_3803+360 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247376 | |||||
| chr4:105247466
|
C | G | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3803+3688C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247466 | ||||||
| chr4:105247526
|
T | G | 1 | a0001c0001t0070g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3803+3748T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247526 | ||||||
| chr4:105247579
|
C | G | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3803+3801C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247579 | ||||||
| chr4:105247642
|
GTTTAC | G | 223 | a0001c0001t0001g0274a0001c0001t0002g0254a0001c0001t0003g0159others(220): Show | 223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.3803+3869_3803+387 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247642 | |||||
| chr4:105247664
|
A | G | 2 | a0003c0004t0016g0072a0003c0004t0016g0073 | 2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3803+3886A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247664 | ||||||
| chr4:105247714
|
C | CT | 16 | a0001c0001t0001g0219a0001c0001t0001g0256a0001c0001t0001g0257others(13): Show | 16 | HG00558.hp2 HG00738.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.3803+3961dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247714 | |||||
| chr4:105247714
|
C | CTT | 10 | a0001c0007t0032g0116a0001c0007t0032g0340a0001c0007t0033g0036others(7): Show | 10 | HG00735.hp2 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3803+3960_3803+396 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247714 | |||||
| chr4:105247714
|
CT | C | 168 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(165): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3803+3961delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247714 | |||||
| chr4:105247714
|
CTT | C | 9 | a0002c0002t0003g0133a0002c0002t0003g0231a0002c0002t0037g0148others(6): Show | 9 | HG01169.hp2 HG01516.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.3803+3960_3803+396 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247714 | |||||
| chr4:105247723
|
T | C | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3803+3945T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247723 | ||||||
| chr4:105247898
|
T | G | 45 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(42): Show | 45 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.3803+4120T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247898 | ||||||
| chr4:105248136
|
T | C | 3 | a0005c0005t0012g0069a0005c0005t0012g0070a0005c0005t0029g0068 | 3 | HG02970.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3803+4358T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248136 | ||||||
| chr4:105248392
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+4614A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248392 | ||||||
| chr4:105248668
|
C | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3803+4890C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248668 | ||||||
| chr4:105248766
|
C | T | 44 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(41): Show | 44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.3803+4988C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248766 | ||||||
| chr4:105248909
|
A | T | 3 | a0003c0004t0083g0047a0012c0014t0060g0049a0012c0014t0064g0048 | 3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3803+5131A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248909 | ||||||
| chr4:105248914
|
G | A | 26 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(23): Show | 26 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.3803+5136G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248914 | ||||||
| chr4:105248936
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+5158A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248936 | ||||||
| chr4:105249001
|
C | CT | 79 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0266others(76): Show | 79 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.3803+5237dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105249001 | |||||
| chr4:105249001
|
CT | C | 27 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(24): Show | 27 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.3803+5237delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105249001 | |||||
| chr4:105249022
|
G | A | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3803+5244G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249022 | ||||||
| chr4:105249077
|
G | A | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3803+5299G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249077 | ||||||
| chr4:105249154
|
G | A | 1 | a0001c0007t0033g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3803+5376G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249154 | ||||||
| chr4:105249218
|
G | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+5440G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249218 | ||||||
| chr4:105249248
|
A | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+5470A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249248 | ||||||
| chr4:105249325
|
A | T | 1 | a0001c0001t0022g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3803+5547A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249325 | ||||||
| chr4:105249357
|
C | T | 13 | a0002c0002t0003g0127a0002c0002t0003g0152a0002c0002t0003g0153others(10): Show | 13 | HG00558.hp2 HG02056.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3803+5579C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249357 | ||||||
| chr4:105249402
|
A | G | 1 | a0004c0003t0002g0100 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3803+5624A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249402 | ||||||
| chr4:105249510
|
G | A | 1 | a0003c0004t0093g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3803+5732G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249510 | ||||||
| chr4:105249713
|
G | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+5935G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249713 | ||||||
| chr4:105249919
|
A | G | 44 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(41): Show | 44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.3803+6141A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249919 | ||||||
| chr4:105249966
|
A | G | 1 | a0001c0001t0007g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3803+6188A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249966 | ||||||
| chr4:105250361
|
T | C | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG01243.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3803+6583T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250361 | ||||||
| chr4:105250380
|
A | AT | 37 | a0001c0001t0001g0111a0001c0001t0001g0219a0001c0001t0001g0256others(34): Show | 37 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.3803+6633dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
A | ATT | 13 | a0001c0001t0001g0240a0001c0001t0001g0279a0001c0001t0001g0284others(10): Show | 13 | HG01099.hp2 HG01258.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.3803+6632_3803+663 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
A | ATTTTT | 9 | a0001c0001t0001g0189a0001c0001t0005g0190a0001c0001t0005g0191others(6): Show | 9 | HG00642.hp2 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.3803+6629_3803+663 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
AT | A | 38 | a0001c0001t0001g0286a0003c0004t0083g0047a0004c0003t0002g0076others(35): Show | 38 | HG00438.hp1 HG00544.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.3803+6633delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
ATT | A | 18 | a0001c0001t0002g0253a0001c0001t0038g0027a0003c0004t0099g0064others(15): Show | 18 | HG01070.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3803+6632_3803+663 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
ATTTT | A | 31 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(28): Show | 31 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.3803+6630_3803+663 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
ATTTTTT | A | 13 | a0001c0001t0006g0204a0001c0001t0006g0206a0001c0001t0006g0212others(10): Show | 13 | HG00323.hp2 HG00735.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3803+6628_3803+663 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
ATTTTTTT | A | 29 | a0001c0001t0004g0209a0001c0001t0006g0207a0001c0001t0006g0214others(26): Show | 29 | HG00609.hp1 HG00642.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.3803+6627_3803+663 others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
ATTTTTTT others(1): Show |
A | 61 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0009g0129others(58): Show | 61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.3803+6626_3803+663 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
ATTTTTTT others(3): Show |
A | 11 | a0003c0004t0030g0202a0003c0011t0007g0326a0003c0011t0042g0329others(8): Show | 11 | HG02809.hp2 HG02818.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.3803+6624_3803+663 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250380
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3803+6622_3803+663 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | |||||
| chr4:105250478
|
T | G | 161 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(158): Show | 161 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.3803+6700T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250478 | ||||||
| chr4:105250495
|
A | T | 159 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(156): Show | 159 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.3803+6717A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250495 | ||||||
| chr4:105250702
|
A | T | 27 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(24): Show | 27 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.3803+6924A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250702 | ||||||
| chr4:105250714
|
A | G | 1 | a0001c0001t0008g0302 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3803+6936A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250714 | ||||||
| chr4:105250826
|
C | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+7048C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250826 | ||||||
| chr4:105250827
|
G | A | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3803+7049G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250827 | ||||||
| chr4:105251126
|
A | G | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3803+7348A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251126 | ||||||
| chr4:105251294
|
A | G | 44 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(41): Show | 44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.3803+7516A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251294 | ||||||
| chr4:105251480
|
A | C | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+7702A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251480 | ||||||
| chr4:105251495
|
C | T | 1 | a0001c0001t0005g0191 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3803+7717C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251495 | ||||||
| chr4:105251590
|
C | T | 1 | a0001c0001t0008g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3803+7812C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251590 | ||||||
| chr4:105251626
|
CTGTT | C | 72 | a0001c0001t0003g0159a0001c0001t0009g0129a0001c0001t0009g0151others(69): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.3803+7851_3803+785 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105251626 | |||||
| chr4:105251827
|
C | A | 3 | a0001c0001t0005g0193a0001c0001t0005g0196a0001c0001t0043g0198 | 3 | HG00741.hp1 HG01123.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3804-7792C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251827 | ||||||
| chr4:105251940
|
G | T | 1 | a0002c0002t0003g0345 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3804-7679G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251940 | ||||||
| chr4:105252020
|
G | T | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3804-7599G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252020 | ||||||
| chr4:105252042
|
A | C | 228 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0002g0253others(225): Show | 228 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.3804-7577A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252042 | ||||||
| chr4:105252152
|
T | G | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3804-7467T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252152 | ||||||
| chr4:105252174
|
C | T | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3804-7445C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252174 | ||||||
| chr4:105252216
|
A | G | 4 | a0001c0001t0004g0323a0001c0001t0015g0271a0001c0001t0015g0291others(1): Show | 4 | HG01928.hp2 HG02004.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.3804-7403A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252216 | ||||||
| chr4:105252223
|
T | G | 1 | a0001c0001t0070g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3804-7396T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252223 | ||||||
| chr4:105252300
|
G | A | 1 | a0003c0004t0004g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3804-7319G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252300 | ||||||
| chr4:105252383
|
T | C | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3804-7236T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252383 | ||||||
| chr4:105252628
|
A | C | 1 | a0004c0003t0002g0108 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3804-6991A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252628 | ||||||
| chr4:105252872
|
G | A | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3804-6747G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252872 | ||||||
| chr4:105253225
|
A | G | 2 | a0002c0002t0003g0142a0002c0002t0003g0145 | 2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.3804-6394A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253225 | ||||||
| chr4:105253309
|
A | G | 1 | a0004c0003t0002g0090 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3804-6310A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253309 | ||||||
| chr4:105253317
|
A | G | 1 | a0001c0001t0040g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3804-6302A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253317 | ||||||
| chr4:105253442
|
T | G | 1 | a0002c0002t0084g0075 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3804-6177T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253442 | ||||||
| chr4:105253546
|
G | GT | 58 | a0001c0001t0003g0159a0001c0001t0009g0129a0001c0001t0009g0151others(55): Show | 58 | HG01106.hp2 HG01109.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.3804-6060dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105253546 | |||||
| chr4:105253674
|
A | T | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.3804-5945A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253674 | ||||||
| chr4:105253779
|
T | C | 166 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(163): Show | 166 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.3804-5840T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253779 | ||||||
| chr4:105254084
|
A | G | 1 | a0001c0001t0007g0305 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3804-5535A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254084 | ||||||
| chr4:105254191
|
T | C | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3804-5428T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254191 | ||||||
| chr4:105254356
|
G | C | 6 | a0003c0004t0058g0313a0003c0004t0083g0047a0003c0004t0105g0050others(3): Show | 6 | HG03130.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.3804-5263G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254356 | ||||||
| chr4:105254428
|
T | A | 1 | a0001c0001t0054g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3804-5191T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254428 | ||||||
| chr4:105254445
|
C | G | 1 | a0003c0004t0041g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3804-5174C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254445 | ||||||
| chr4:105254477
|
T | A | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3804-5142T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254477 | ||||||
| chr4:105254747
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3804-4872A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254747 | ||||||
| chr4:105254753
|
C | T | 1 | a0001c0001t0007g0305 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3804-4866C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254753 | ||||||
| chr4:105254761
|
A | G | 2 | a0007c0009t0052g0031a0007c0009t0055g0039 | 2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3804-4858A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254761 | ||||||
| chr4:105254963
|
T | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3804-4656T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254963 | ||||||
| chr4:105255215
|
C | T | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3804-4404C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255215 | ||||||
| chr4:105255236
|
G | C | 1 | a0001c0001t0008g0302 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3804-4383G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255236 | ||||||
| chr4:105255450
|
A | G | 9 | a0001c0001t0070g0032a0001c0007t0032g0116a0001c0007t0032g0340others(6): Show | 9 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3804-4169A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255450 | ||||||
| chr4:105255648
|
A | T | 2 | a0004c0003t0002g0099a0004c0003t0002g0105 | 2 | NA18951.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.3804-3971A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255648 | ||||||
| chr4:105255919
|
T | TTTATG | 5 | a0003c0004t0030g0202a0003c0011t0007g0326a0003c0011t0042g0329others(2): Show | 5 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3804-3699_3804-369 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105255919 | |||||
| chr4:105255921
|
G | GATGTT | 223 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0002g0253others(220): Show | 223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.3804-3697_3804-369 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105255921 | |||||
| chr4:105255921
|
G | T | 5 | a0003c0004t0030g0202a0003c0011t0007g0326a0003c0011t0042g0329others(2): Show | 5 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3804-3698G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255921 | ||||||
| chr4:105256295
|
A | G | 1 | a0003c0011t0049g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3804-3324A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256295 | ||||||
| chr4:105256315
|
C | A | 1 | a0002c0002t0037g0136 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3804-3304C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256315 | ||||||
| chr4:105256330
|
G | C | 2 | a0002c0002t0020g0171a0002c0002t0020g0172 | 2 | HG00280.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.3804-3289G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256330 | ||||||
| chr4:105256607
|
G | A | 6 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0297others(3): Show | 6 | HG01255.hp2 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.3804-3012G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256607 | ||||||
| chr4:105256657
|
G | A | 14 | a0003c0004t0004g0033a0003c0004t0021g0034a0003c0004t0058g0313others(11): Show | 14 | HG01175.hp1 HG01891.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.3804-2962G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256657 | ||||||
| chr4:105256684
|
A | G | 6 | a0003c0004t0058g0313a0003c0004t0083g0047a0003c0004t0105g0050others(3): Show | 6 | HG03130.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.3804-2935A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256684 | ||||||
| chr4:105256725
|
G | A | 40 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(37): Show | 40 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.3804-2894G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256725 | ||||||
| chr4:105256916
|
A | G | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3804-2703A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256916 | ||||||
| chr4:105256997
|
A | G | 5 | a0003c0008t0019g0330a0003c0008t0019g0333a0003c0008t0059g0324others(2): Show | 5 | HG02572.hp2 HG06807.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.3804-2622A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256997 | ||||||
| chr4:105257132
|
A | C | 159 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(156): Show | 159 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.3804-2487A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257132 | ||||||
| chr4:105257139
|
A | T | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3804-2480A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257139 | ||||||
| chr4:105257216
|
T | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3804-2403T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257216 | ||||||
| chr4:105257316
|
T | C | 50 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0013g0331others(47): Show | 50 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.3804-2303T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257316 | ||||||
| chr4:105257471
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3804-2148T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257471 | ||||||
| chr4:105257745
|
A | G | 157 | a0001c0001t0001g0237a0001c0001t0003g0159a0001c0001t0004g0203others(154): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.3804-1874A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257745 | ||||||
| chr4:105258069
|
T | G | 2 | a0001c0001t0085g0029a0001c0001t0087g0028 | 2 | HG01361.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3804-1550T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258069 | ||||||
| chr4:105258297
|
CAT | C | 73 | a0001c0001t0003g0159a0001c0001t0009g0129a0001c0001t0009g0151others(70): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.3804-1321_3804-132 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258297 | ||||||
| chr4:105258381
|
C | T | 9 | a0001c0001t0070g0032a0001c0007t0032g0116a0001c0007t0032g0340others(6): Show | 9 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3804-1238C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258381 | ||||||
| chr4:105258474
|
ATTATAT | A | 4 | a0008c0010t0011g0007a0008c0010t0011g0008a0008c0010t0011g0010others(1): Show | 4 | HG02145.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3804-1141_3804-113 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105258474 | |||||
| chr4:105258484
|
G | C | 1 | a0004c0003t0013g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3804-1135G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258484 | ||||||
| chr4:105258550
|
A | G | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3804-1069A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258550 | ||||||
| chr4:105258857
|
T | C | 1 | a0002c0002t0003g0133 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3804-762T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258857 | ||||||
| chr4:105259107
|
T | C | 270 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(267): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3804-512T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259107 | ||||||
| chr4:105259165
|
C | T | 1 | a0001c0001t0015g0271 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3804-454C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259165 | ||||||
| chr4:105259169
|
T | C | 1 | a0003c0004t0105g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3804-450T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259169 | ||||||
| chr4:105259550
|
C | A | 1 | a0001c0001t0001g0251 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3804-69C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259550 | ||||||
| chr4:105259585
|
C | A | 3 | a0004c0003t0021g0117a0005c0005t0005g0040a0005c0005t0005g0041 | 3 | HG01070.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3804-34C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259585 | ||||||
| chr4:105259588
|
T | C | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | NA18941.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3804-31T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259588 | ||||||
| chr4:105259795
|
C | A | 1 | a0008c0010t0011g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3954+26C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105259795 | ||||||
| chr4:105259997
|
A | T | 1 | a0004c0003t0002g0100 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3954+228A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105259997 | ||||||
| chr4:105260083
|
T | C | 1 | a0003c0018t0019g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3954+314T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260083 | ||||||
| chr4:105260150
|
T | TTAAAGTC others(20): Show |
2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3954+409_3954+435d others(29): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr4 | 105260150 | |||||
| chr4:105260233
|
ACT | A | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3954+467_3954+468d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr4 | 105260233 | |||||
| chr4:105260266
|
T | A | 1 | a0001c0001t0005g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3954+497T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260266 | ||||||
| chr4:105260413
|
G | A | 6 | a0002c0002t0003g0132a0002c0002t0025g0131a0002c0002t0025g0138others(3): Show | 6 | HG00738.hp1 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.3954+644G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260413 | ||||||
| chr4:105260416
|
G | A | 106 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(103): Show | 106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.3954+647G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260416 | ||||||
| chr4:105260462
|
T | TA | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3954+703dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr4 | 105260462 | |||||
| chr4:105260470
|
A | G | 4 | a0002c0002t0003g0126a0002c0002t0003g0178a0002c0023t0003g0144others(1): Show | 4 | HG00544.hp2 NA18959.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3954+701A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260470 | ||||||
| chr4:105260472
|
AC | A | 5 | a0004c0003t0021g0117a0008c0010t0011g0007a0008c0010t0011g0008others(2): Show | 5 | HG01070.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3954+704delC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260472 | ||||||
| chr4:105260600
|
C | T | 2 | a0002c0002t0027g0157a0002c0002t0027g0169 | 2 | NA18955.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3954+831C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260600 | ||||||
| chr4:105260669
|
T | C | 1 | a0001c0001t0008g0293 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3954+900T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260669 | ||||||
| chr4:105260723
|
T | G | 2 | a0002c0002t0026g0173a0006c0006t0068g0013 | 2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3954+954T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260723 | ||||||
| chr4:105260975
|
A | T | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3955-784A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260975 | ||||||
| chr4:105261111
|
C | A | 1 | a0001c0007t0032g0340 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3955-648C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261111 | ||||||
| chr4:105261163
|
T | C | 2 | a0003c0004t0035g0062a0003c0004t0044g0063 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3955-596T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261163 | ||||||
| chr4:105261167
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3955-592A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261167 | ||||||
| chr4:105261289
|
A | G | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3955-470A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261289 | ||||||
| chr4:105261321
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3955-438C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261321 | ||||||
| chr4:105261372
|
A | C | 1 | a0006c0006t0096g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3955-387A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261372 | ||||||
| chr4:105261437
|
A | T | 1 | a0002c0002t0003g0345 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3955-322A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261437 | ||||||
| chr4:105261448
|
G | A | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3955-311G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261448 | ||||||
| chr4:105261556
|
G | GA | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3955-196dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr4 | 105261556 | |||||
| chr4:105261707
|
A | G | 1 | a0001c0001t0011g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3955-52A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261707 | ||||||
| chr4:105261958
|
C | T | 1 | a0002c0002t0003g0132 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4044+110C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105261958 | ||||||
| chr4:105262084
|
A | G | 1 | a0004c0003t0002g0234 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4044+236A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262084 | ||||||
| chr4:105262134
|
A | G | 1 | a0002c0002t0003g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4044+286A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262134 | ||||||
| chr4:105262266
|
A | G | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4044+418A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262266 | ||||||
| chr4:105262317
|
T | C | 229 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0002g0253others(226): Show | 229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.4044+469T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262317 | ||||||
| chr4:105262365
|
A | AT | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.4044+527dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105262365 | |||||
| chr4:105262365
|
AT | A | 48 | a0001c0001t0006g0242a0001c0001t0038g0027a0003c0004t0004g0033others(45): Show | 48 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.4044+527delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105262365 | |||||
| chr4:105262487
|
T | C | 1 | a0002c0002t0010g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4044+639T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262487 | ||||||
| chr4:105262623
|
T | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4044+775T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262623 | ||||||
| chr4:105262664
|
C | T | 1 | a0003c0004t0039g0225 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4044+816C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262664 | ||||||
| chr4:105262773
|
C | T | 1 | a0001c0001t0007g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4044+925C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262773 | ||||||
| chr4:105262774
|
G | A | 1 | a0003c0004t0017g0320 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4044+926G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262774 | ||||||
| chr4:105262829
|
C | T | 1 | a0001c0001t0005g0191 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4044+981C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262829 | ||||||
| chr4:105262857
|
G | T | 14 | a0003c0004t0004g0033a0003c0004t0021g0034a0003c0004t0058g0313others(11): Show | 14 | HG01175.hp1 HG01891.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.4044+1009G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262857 | ||||||
| chr4:105262881
|
C | CA | 93 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0002g0253others(90): Show | 93 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.4044+1048dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105262881 | |||||
| chr4:105262885
|
A | G | 1 | a0001c0001t0080g0298 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4044+1037A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262885 | ||||||
| chr4:105262916
|
G | A | 5 | a0001c0001t0004g0186a0001c0001t0008g0195a0001c0001t0008g0199others(2): Show | 5 | HG00642.hp2 HG00741.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.4044+1068G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262916 | ||||||
| chr4:105263014
|
G | C | 2 | a0003c0008t0019g0333a0003c0008t0066g0328 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4044+1166G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263014 | ||||||
| chr4:105263028
|
T | TA | 52 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0005g0270others(49): Show | 52 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.4044+1189dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105263028 | |||||
| chr4:105263028
|
TAAA | T | 104 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.4044+1187_4044+118 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105263028 | |||||
| chr4:105263072
|
C | T | 104 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.4044+1224C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263072 | ||||||
| chr4:105263078
|
CATATAAA | C | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4044+1234_4044+124 others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105263078 | |||||
| chr4:105263220
|
G | A | 1 | a0001c0001t0004g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4044+1372G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263220 | ||||||
| chr4:105263440
|
A | C | 106 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(103): Show | 106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.4044+1592A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263440 | ||||||
| chr4:105263564
|
T | A | 2 | a0012c0014t0060g0049a0012c0014t0064g0048 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4044+1716T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263564 | ||||||
| chr4:105263607
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4044+1759T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263607 | ||||||
| chr4:105263946
|
G | A | 1 | a0004c0003t0002g0101 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4044+2098G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263946 | ||||||
| chr4:105264083
|
G | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4044+2235G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264083 | ||||||
| chr4:105264092
|
C | CA | 269 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.4044+2244_4044+224 others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264092 | ||||||
| chr4:105264102
|
A | AT | 27 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(24): Show | 27 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.4044+2269dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105264102 | |||||
| chr4:105264102
|
AT | A | 9 | a0001c0001t0001g0258a0001c0001t0001g0272a0001c0001t0001g0273others(6): Show | 9 | HG00438.hp2 HG03704.hp1 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.4044+2269delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105264102 | |||||
| chr4:105264114
|
T | C | 1 | a0002c0002t0003g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4044+2266T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264114 | ||||||
| chr4:105264118
|
G | C | 110 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0003g0159others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.4044+2270G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264118 | ||||||
| chr4:105264157
|
G | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4044+2309G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264157 | ||||||
| chr4:105264233
|
A | T | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4044+2385A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264233 | ||||||
| chr4:105264256
|
G | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4044+2408G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264256 | ||||||
| chr4:105264273
|
A | G | 8 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0005g0187others(5): Show | 8 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.4044+2425A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264273 | ||||||
| chr4:105264299
|
C | T | 266 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.4044+2451C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264299 | ||||||
| chr4:105264371
|
A | G | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4044+2523A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264371 | ||||||
| chr4:105264500
|
A | T | 9 | a0001c0001t0070g0032a0001c0007t0032g0116a0001c0007t0032g0340others(6): Show | 9 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.4044+2652A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264500 | ||||||
| chr4:105264506
|
C | T | 265 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0232others(262): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.4044+2658C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264506 | ||||||
| chr4:105264865
|
G | T | 1 | a0006c0006t0048g0003 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4044+3017G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264865 | ||||||
| chr4:105264902
|
T | C | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4044+3054T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264902 | ||||||
| chr4:105265144
|
G | A | 51 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0013g0331others(48): Show | 51 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.4044+3296G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265144 | ||||||
| chr4:105265220
|
T | C | 1 | a0001c0007t0032g0340 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4044+3372T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265220 | ||||||
| chr4:105265348
|
C | G | 1 | a0006c0006t0065g0341 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4044+3500C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265348 | ||||||
| chr4:105265590
|
T | A | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4044+3742T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265590 | ||||||
| chr4:105265897
|
T | C | 1 | a0008c0010t0011g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4045-3713T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265897 | ||||||
| chr4:105266216
|
A | T | 1 | a0002c0002t0003g0345 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4045-3394A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105266216 | ||||||
| chr4:105266252
|
T | C | 1 | a0002c0002t0084g0075 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4045-3358T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105266252 | ||||||
| chr4:105266524
|
T | G | 1 | a0004c0003t0002g0108 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4045-3086T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105266524 | ||||||
| chr4:105267099
|
A | G | 3 | a0001c0001t0073g0025a0001c0001t0075g0024a0001c0001t0076g0023 | 3 | HG02004.hp2 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4045-2511A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267099 | ||||||
| chr4:105267391
|
A | T | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-2219A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267391 | ||||||
| chr4:105267535
|
C | A | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4045-2075C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267535 | ||||||
| chr4:105267539
|
T | TA | 13 | a0001c0001t0004g0323a0004c0003t0002g0112a0005c0005t0005g0055others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.4045-2055dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105267539 | |||||
| chr4:105267539
|
TA | T | 162 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(159): Show | 162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.4045-2055delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105267539 | |||||
| chr4:105267739
|
G | T | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.4045-1871G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267739 | ||||||
| chr4:105267962
|
A | C | 1 | a0003c0004t0105g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4045-1648A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267962 | ||||||
| chr4:105267999
|
C | A | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-1611C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267999 | ||||||
| chr4:105268101
|
A | AAT | 4 | a0005c0005t0012g0069a0005c0005t0012g0070a0005c0005t0012g0071others(1): Show | 4 | HG02970.hp2 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4045-1507_4045-150 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105268101 | |||||
| chr4:105268137
|
C | G | 5 | a0003c0004t0030g0202a0003c0011t0007g0326a0003c0011t0042g0329others(2): Show | 5 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4045-1473C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268137 | ||||||
| chr4:105268333
|
C | CA | 8 | a0001c0007t0032g0116a0001c0007t0032g0340a0001c0007t0033g0036others(5): Show | 8 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.4045-1272dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105268333 | |||||
| chr4:105268355
|
C | T | 2 | a0012c0014t0060g0049a0012c0014t0064g0048 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4045-1255C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268355 | ||||||
| chr4:105268457
|
G | T | 107 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.4045-1153G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268457 | ||||||
| chr4:105268736
|
C | T | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-874C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268736 | ||||||
| chr4:105268898
|
A | G | 107 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0005g0270others(104): Show | 107 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.4045-712A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268898 | ||||||
| chr4:105269069
|
C | T | 114 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.4045-541C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269069 | ||||||
| chr4:105269282
|
G | A | 3 | a0002c0002t0003g0124a0002c0002t0003g0125a0002c0002t0003g0134 | 3 | NA19003.hp1 NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.4045-328G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269282 | ||||||
| chr4:105269300
|
A | G | 1 | a0003c0008t0067g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4045-310A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269300 | ||||||
| chr4:105269556
|
G | A | 4 | a0001c0001t0001g0219a0001c0001t0001g0256a0001c0001t0001g0284others(1): Show | 4 | HG02027.hp1 HG02165.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.4045-54G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269556 | ||||||
| chr4:105269573
|
A | G | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0004g0309others(1): Show | 4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.4045-37A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269573 | ||||||
| chr4:105269575
|
C | A | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-35C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269575 | ||||||
| chr4:105269583
|
G | A | 9 | a0005c0005t0005g0055a0005c0005t0012g0069a0005c0005t0012g0070others(6): Show | 9 | HG02280.hp1 HG02615.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.4045-27G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269583 | ||||||
| chr4:105269756
|
G | A | 1 | a0002c0002t0003g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4182+9G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105269756 | ||||||
| chr4:105269994
|
C | T | 9 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(6): Show | 9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.4182+247C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105269994 | ||||||
| chr4:105270267
|
G | A | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4182+520G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270267 | ||||||
| chr4:105270434
|
G | C | 1 | a0003c0019t0079g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4182+687G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270434 | ||||||
| chr4:105270510
|
C | G | 2 | a0002c0002t0027g0157a0002c0002t0027g0169 | 2 | NA18955.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.4182+763C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270510 | ||||||
| chr4:105270523
|
A | G | 10 | a0005c0005t0005g0030a0005c0005t0005g0040a0005c0005t0005g0041others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.4182+776A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270523 | ||||||
| chr4:105270579
|
A | T | 46 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(43): Show | 46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.4182+832A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270579 | ||||||
| chr4:105270586
|
G | A | 1 | a0003c0031t0091g0019 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4182+839G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270586 | ||||||
| chr4:105270642
|
G | A | 2 | a0011c0015t0045g0348a0011c0015t0046g0347 | 2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.4182+895G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270642 | ||||||
| chr4:105270663
|
A | G | 1 | a0001c0001t0078g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4182+916A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270663 | ||||||
| chr4:105270674
|
T | TTA | 13 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(10): Show | 13 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.4182+951_4182+952d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | |||||
| chr4:105270674
|
T | TTATA | 7 | a0001c0001t0001g0259a0001c0001t0001g0266a0001c0001t0001g0267others(4): Show | 7 | HG03239.hp1 HG03654.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.4182+949_4182+952d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | |||||
| chr4:105270674
|
TTA | T | 35 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(32): Show | 35 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.4182+951_4182+952d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | |||||
| chr4:105270674
|
TTATA | T | 8 | a0003c0004t0035g0119a0006c0006t0028g0004a0006c0006t0028g0006others(5): Show | 8 | HG01192.hp1 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4182+949_4182+952d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | |||||
| chr4:105270674
|
TTATATA | T | 112 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0013g0331others(109): Show | 112 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.4182+947_4182+952d others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | |||||
| chr4:105270674
|
TTATATAT others(1): Show |
T | 104 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.4182+945_4182+952d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | |||||
| chr4:105270681
|
T | C | 1 | a0003c0004t0035g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4182+934T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270681 | ||||||
| chr4:105270683
|
T | C | 45 | a0003c0004t0004g0033a0003c0004t0016g0072a0003c0004t0016g0073others(42): Show | 45 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.4182+936T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270683 | ||||||
| chr4:105270922
|
G | C | 2 | a0003c0004t0016g0072a0003c0004t0016g0073 | 2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4182+1175G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270922 | ||||||
| chr4:105271057
|
T | C | 1 | a0001c0001t0038g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4182+1310T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271057 | ||||||
| chr4:105271067
|
C | T | 2 | a0002c0002t0001g0130a0002c0002t0008g0317 | 2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.4182+1320C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271067 | ||||||
| chr4:105271147
|
A | G | 1 | a0001c0001t0092g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4182+1400A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271147 | ||||||
| chr4:105271229
|
T | A | 1 | a0004c0003t0002g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4183-1335T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271229 | ||||||
| chr4:105271235
|
A | G | 26 | a0003c0004t0016g0072a0003c0004t0016g0073a0003c0004t0016g0222others(23): Show | 26 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.4183-1329A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271235 | ||||||
| chr4:105271300
|
C | A | 40 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(37): Show | 40 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.4183-1264C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271300 | ||||||
| chr4:105271308
|
T | A | 1 | a0001c0001t0004g0323 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.4183-1256T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271308 | ||||||
| chr4:105271406
|
T | C | 40 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0004g0186others(37): Show | 40 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.4183-1158T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271406 | ||||||
| chr4:105271445
|
AG | A | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.4183-1118delG | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271445 | ||||||
| chr4:105271618
|
G | A | 224 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0003g0159others(221): Show | 224 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.4183-946G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271618 | ||||||
| chr4:105272003
|
C | G | 111 | a0001c0001t0001g0237a0001c0001t0003g0159a0001c0001t0004g0203others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.4183-561C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272003 | ||||||
| chr4:105272015
|
AT | A | 22 | a0001c0001t0004g0203a0001c0001t0004g0209a0001c0001t0006g0204others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.4183-543delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105272015 | |||||
| chr4:105272177
|
T | C | 113 | a0001c0001t0001g0237a0001c0001t0003g0159a0001c0001t0004g0203others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.4183-387T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272177 | ||||||
| chr4:105272378
|
T | C | 1 | a0001c0001t0009g0129 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4183-186T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272378 | ||||||
| chr4:105272431
|
A | G | 55 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0005g0270others(52): Show | 55 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.4183-133A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272431 | ||||||
| chr4:105272493
|
A | G | 1 | a0002c0002t0003g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4183-71A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272493 | ||||||
| chr4:105272994
|
C | T | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4537+76C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105272994 | ||||||
| chr4:105273189
|
C | T | 2 | a0013c0016t0001g0017a0013c0016t0001g0018 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4537+271C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273189 | ||||||
| chr4:105273262
|
C | A | 7 | a0006c0006t0028g0004a0006c0006t0028g0006a0006c0006t0028g0009others(4): Show | 7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4537+344C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273262 | ||||||
| chr4:105273315
|
C | T | 1 | a0014c0017t0003g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4537+397C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273315 | ||||||
| chr4:105273485
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0004g0299 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.4537+567C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273485 | ||||||
| chr4:105273703
|
T | C | 1 | a0003c0004t0105g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4537+785T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273703 | ||||||
| chr4:105273764
|
T | G | 8 | a0006c0006t0024g0336a0006c0006t0024g0339a0006c0006t0024g0342others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4537+846T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273764 | ||||||
| chr4:105273869
|
T | C | 55 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0005g0270others(52): Show | 55 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.4537+951T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273869 | ||||||
| chr4:105273879
|
A | G | 1 | a0003c0004t0016g0222 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4537+961A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273879 | ||||||
| chr4:105273886
|
C | G | 1 | a0016c0021t0004g0346 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4537+968C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273886 | ||||||
| chr4:105274023
|
T | G | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4538-1025T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274023 | ||||||
| chr4:105274185
|
T | C | 1 | a0003c0011t0007g0326 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4538-863T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274185 | ||||||
| chr4:105274210
|
C | G | 1 | a0001c0001t0074g0021 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4538-838C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274210 | ||||||
| chr4:105274263
|
A | G | 1 | a0003c0004t0105g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4538-785A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274263 | ||||||
| chr4:105274279
|
A | T | 10 | a0001c0001t0070g0032a0001c0001t0108g0002a0001c0007t0032g0116others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.4538-769A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274279 | ||||||
| chr4:105274384
|
T | C | 266 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0002g0253others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.4538-664T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274384 | ||||||
| chr4:105274415
|
G | A | 105 | a0001c0001t0003g0159a0001c0001t0004g0203a0001c0001t0004g0209others(102): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.4538-633G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274415 | ||||||
| chr4:105274434
|
G | C | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4538-614G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274434 | ||||||
| chr4:105274491
|
T | G | 2 | a0012c0014t0060g0049a0012c0014t0064g0048 | 2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4538-557T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274491 | ||||||
| chr4:105274609
|
T | G | 1 | a0015c0020t0069g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4538-439T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274609 | ||||||
| chr4:105274680
|
G | C | 1 | a0001c0001t0006g0242 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4538-368G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274680 | ||||||
| chr4:105274690
|
C | T | 5 | a0001c0001t0072g0022a0001c0001t0073g0025a0001c0001t0074g0021others(2): Show | 5 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.4538-358C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274690 | ||||||
| chr4:105274691
|
G | C | 1 | a0001c0001t0108g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4538-357G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274691 | ||||||
| chr4:105274693
|
T | C | 52 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0005g0270others(49): Show | 52 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.4538-355T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274693 | ||||||
| chr4:105274728
|
T | C | 4 | a0002c0002t0001g0130a0002c0002t0003g0133a0002c0002t0008g0317others(1): Show | 4 | HG02698.hp1 HG03017.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.4538-320T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274728 | ||||||
| chr4:105274736
|
G | A | 2 | a0001c0001t0085g0029a0001c0001t0087g0028 | 2 | HG01361.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4538-312G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274736 | ||||||
| chr4:105274830
|
A | AT | 6 | a0001c0001t0072g0022a0001c0001t0073g0025a0001c0001t0074g0021others(3): Show | 6 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.4538-208dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr4 | 105274830 | |||||
| chr4:105274935
|
C | T | 284 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0241others(281): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.4538-113C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274935 |