Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 80746 |
|---|---|
| ensemblid | ENSG00000154743.19 |
| hgncid | 28422 |
| symbol | TSEN2 |
| name | tRNA splicing endonuclease subunit 2 |
| refseq_nuc | NM_025265.4 |
| refseq_prot | NP_079541.1 |
| ensembl_nuc | ENST00000284995.11 |
| ensembl_prot | ENSP00000284995.6 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 12484480 |
| end | 12533658 |
| strand | + |
| ver | v1.2 |
| region | chr3:12484480-12533658 |
| region5000 | chr3:12479480-12538658 |
| regionname0 | TSEN2_chr3_12484480_12533658 |
| regionname5000 | TSEN2_chr3_12479480_12538658 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 465 | 223 | 68 | 49 | 64 | 12 | 28 | 51 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002 | 0/0 | 465 | 37 | 19 | 9 | 7 | 0 | 2 | 5 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0003 | 0/0 | 465 | 23 | 5 | 8 | 3 | 4 | 3 | 2 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0004 | 0/0 | 465 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1398 | 206 | 58 | 43 | 64 | 12 | 27 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0002 | 0/0 | 1398 | 23 | 5 | 8 | 3 | 4 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0003 | 0/0 | 1398 | 19 | 16 | 3 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0004 | 0/0 | 1398 | 15 | 0 | 6 | 7 | 0 | 2 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0005 | 0/0 | 1398 | 9 | 3 | 6 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0006 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0007 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0008 | 0/0 | 1398 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0009 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0010 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0011 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| c0012 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1356 | 93 | 9 | 18 | 40 | 7 | 17 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0002 | 0/0 | 1356 | 88 | 46 | 13 | 22 | 2 | 5 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0003 | 0/0 | 1356 | 31 | 8 | 13 | 3 | 4 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0004 | 0/0 | 1356 | 19 | 13 | 5 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0005 | 0/0 | 1356 | 13 | 6 | 2 | 1 | 1 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0006 | 0/0 | 1356 | 11 | 2 | 3 | 5 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0007 | 0/0 | 1356 | 8 | 0 | 6 | 2 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0008 | 0/0 | 1356 | 5 | 5 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0009 | 0/0 | 1356 | 4 | 0 | 0 | 1 | 0 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0010 | 0/0 | 1356 | 2 | 0 | 1 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0011 | 0/0 | 1356 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0012 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0013 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0014 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0015 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0016 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0017 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0018 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| t0019 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| 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 | 11 | 0 | 2 | 4 | 2 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0004 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0006 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1398 | 206 | 58 | 43 | 64 | 12 | 27 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0005 | 0/0 | 1398 | 9 | 3 | 6 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0007 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0008 | 0/0 | 1398 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0010 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0011 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0012 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0003 | 0/0 | 1398 | 19 | 16 | 3 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0004 | 0/0 | 1398 | 15 | 0 | 6 | 7 | 0 | 2 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0006 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0003c0002 | 0/0 | 1398 | 23 | 5 | 8 | 3 | 4 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0004c0009 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2753 | 88 | 8 | 18 | 36 | 7 | 17 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0002 | 0/0 | 2753 | 74 | 34 | 11 | 22 | 2 | 5 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0004 | 0/0 | 2753 | 9 | 4 | 4 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0005 | 0/0 | 2753 | 10 | 3 | 2 | 1 | 1 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0006 | 0/0 | 2753 | 11 | 2 | 3 | 5 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0008 | 0/0 | 2753 | 5 | 5 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0010 | 0/0 | 2753 | 2 | 0 | 1 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0011 | 0/0 | 2753 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0013 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0015 | 0/0 | 2753 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0016 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0018 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0001t0019 | 0/0 | 2753 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0005t0003 | 0/0 | 2753 | 9 | 3 | 6 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0007t0004 | 0/0 | 2753 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0008t0002 | 0/0 | 2753 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0010t0001 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0011t0003 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0001c0012t0017 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0003t0002 | 0/0 | 2753 | 12 | 10 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0003t0004 | 0/0 | 2753 | 7 | 6 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0004t0001 | 0/0 | 2753 | 4 | 0 | 0 | 4 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0004t0007 | 0/0 | 2753 | 8 | 0 | 6 | 2 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0004t0009 | 0/0 | 2753 | 3 | 0 | 0 | 1 | 0 | 2 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0002c0006t0005 | 0/0 | 2753 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0003c0002t0003 | 0/0 | 2753 | 21 | 4 | 7 | 3 | 4 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0003c0002t0012 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0003c0002t0014 | 0/0 | 2753 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| a0004c0009t0009 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | copy fasta | chr3 | 12479480 | 12538658 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 2 | 4 | 2 | 3 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0008g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0008g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0010g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0011g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0011g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0013g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0015g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0018g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0001t0019g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0005t0003g0004 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0005t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0005t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0005t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0007t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0007t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0007t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0008t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0008t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0010t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0011t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0001c0012t0017g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0003t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0007g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0007g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0007g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0009g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0009g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0004t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0006t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0006t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0002c0006t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0006 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0003c0002t0014g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| a0004c0009t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0002 | t0003 | g0229 | EUR | GBR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0076 | EUR | GBR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0094 | EUR | GBR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | FIN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00323 | hp2 | a0001 | c0001 | t0016 | g0155 | EUR | FIN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00423 | hp1 | a0003 | c0002 | t0003 | g0215 | EAS | CHS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00639 | hp2 | a0003 | c0002 | t0003 | g0006 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0115 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG00733 | hp2 | a0001 | c0001 | t0010 | g0212 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01069 | hp1 | a0001 | c0005 | t0003 | g0004 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01071 | hp1 | a0001 | c0005 | t0003 | g0004 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01074 | hp2 | a0002 | c0003 | t0002 | g0009 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01081 | hp1 | a0002 | c0003 | t0004 | g0140 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01099 | hp1 | a0002 | c0003 | t0002 | g0009 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01099 | hp2 | a0003 | c0002 | t0003 | g0022 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01167 | hp2 | a0001 | c0005 | t0003 | g0023 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01168 | hp2 | a0001 | c0005 | t0003 | g0004 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01169 | hp2 | a0001 | c0005 | t0003 | g0023 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01175 | hp2 | a0001 | c0005 | t0003 | g0232 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0116 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0090 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01243 | hp2 | a0002 | c0004 | t0007 | g0039 | AMR | PUR | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01256 | hp1 | a0001 | c0001 | t0011 | g0185 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01346 | hp1 | a0001 | c0001 | t0015 | g0081 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0184 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0125 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01515 | hp2 | a0003 | c0002 | t0003 | g0222 | EUR | IBS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0069 | EUR | IBS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01517 | hp1 | a0003 | c0002 | t0003 | g0223 | EUR | IBS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0214 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01891 | hp1 | a0001 | c0005 | t0003 | g0004 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01928 | hp1 | a0003 | c0002 | t0003 | g0226 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01928 | hp2 | a0002 | c0004 | t0007 | g0037 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01934 | hp1 | a0002 | c0004 | t0007 | g0035 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01943 | hp1 | a0003 | c0002 | t0003 | g0228 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01952 | hp1 | a0003 | c0002 | t0003 | g0006 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01978 | hp2 | a0002 | c0004 | t0007 | g0038 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0091 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01993 | hp1 | a0001 | c0001 | t0019 | g0132 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01993 | hp2 | a0003 | c0002 | t0003 | g0230 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02004 | hp1 | a0003 | c0002 | t0014 | g0227 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02004 | hp2 | a0002 | c0004 | t0007 | g0010 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0024 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02129 | hp1 | a0002 | c0004 | t0007 | g0033 | EAS | KHV | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02135 | hp1 | a0002 | c0004 | t0009 | g0040 | EAS | KHV | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02145 | hp1 | a0001 | c0007 | t0004 | g0044 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02258 | hp1 | a0002 | c0003 | t0002 | g0031 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02273 | hp2 | a0003 | c0002 | t0003 | g0006 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0109 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02280 | hp2 | a0001 | c0007 | t0004 | g0047 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02300 | hp2 | a0002 | c0004 | t0007 | g0010 | AMR | PEL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02572 | hp2 | a0002 | c0006 | t0005 | g0236 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02630 | hp1 | a0002 | c0003 | t0002 | g0028 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02630 | hp2 | a0003 | c0002 | t0003 | g0225 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02647 | hp1 | a0002 | c0003 | t0002 | g0030 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02647 | hp2 | a0002 | c0003 | t0004 | g0142 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02717 | hp1 | a0003 | c0002 | t0003 | g0220 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02723 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02723 | hp2 | a0002 | c0006 | t0005 | g0237 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02738 | hp1 | a0003 | c0002 | t0003 | g0219 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02886 | hp2 | a0001 | c0001 | t0018 | g0061 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02895 | hp1 | a0002 | c0003 | t0004 | g0016 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02897 | hp2 | a0002 | c0003 | t0004 | g0016 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03041 | hp1 | a0002 | c0003 | t0002 | g0029 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03130 | hp1 | a0001 | c0005 | t0003 | g0233 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03139 | hp2 | a0001 | c0008 | t0002 | g0087 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03195 | hp1 | a0001 | c0011 | t0003 | g0218 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03209 | hp1 | a0001 | c0007 | t0004 | g0046 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0083 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03486 | hp1 | a0002 | c0003 | t0004 | g0139 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03486 | hp2 | a0002 | c0003 | t0002 | g0025 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03491 | hp2 | a0002 | c0004 | t0009 | g0034 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03516 | hp2 | a0002 | c0003 | t0002 | g0026 | AFR | ESN | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03540 | hp2 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0154 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0096 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03704 | hp1 | a0004 | c0009 | t0009 | g0041 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0117 | SAS | BEB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | BEB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03834 | hp1 | a0003 | c0002 | t0003 | g0231 | SAS | BEB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03927 | hp1 | a0003 | c0002 | t0003 | g0022 | SAS | BEB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0114 | SAS | BEB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0089 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG04228 | hp1 | a0002 | c0004 | t0009 | g0036 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18522 | hp1 | a0001 | c0008 | t0002 | g0086 | AFR | YRI | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18522 | hp2 | a0001 | c0005 | t0003 | g0004 | AFR | YRI | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | YRI | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | YRI | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18947 | hp2 | a0002 | c0004 | t0007 | g0032 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18948 | hp1 | a0002 | c0004 | t0001 | g0147 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18951 | hp2 | a0002 | c0004 | t0001 | g0148 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18962 | hp2 | a0002 | c0004 | t0001 | g0150 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18981 | hp1 | a0003 | c0002 | t0003 | g0216 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19004 | hp2 | a0002 | c0004 | t0001 | g0149 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19007 | hp1 | a0003 | c0002 | t0003 | g0217 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19030 | hp1 | a0002 | c0003 | t0004 | g0138 | AFR | LWK | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | LWK | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19043 | hp1 | a0003 | c0002 | t0012 | g0213 | AFR | LWK | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19043 | hp2 | a0002 | c0003 | t0002 | g0027 | AFR | LWK | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19240 | hp1 | a0001 | c0010 | t0001 | g0151 | AFR | YRI | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | YRI | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ASW | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ASW | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA20805 | hp1 | a0003 | c0002 | t0003 | g0221 | EUR | TSI | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | GIH | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA20905 | hp2 | a0001 | c0012 | t0017 | g0175 | SAS | GIH | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | CLM | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | ACB | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | USA | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| HG06807 | hp2 | a0003 | c0002 | t0003 | g0224 | AFR | USA | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA20300 | hp1 | a0003 | c0002 | t0003 | g0006 | AFR | USA | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA20300 | hp2 | a0002 | c0006 | t0005 | g0238 | AFR | USA | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | LWK | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| NA21309 | hp2 | a0002 | c0003 | t0004 | g0141 | AFR | LWK | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0165 | REF | REF | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0235 | REF | REF | TSEN2_chr3_12479480_12538658 | TSEN2 | chr3 | 12479480 | 12538658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:12484878
|
G | A | 1 | a0001 | 1 | HG02886.hp2 | splice_region_variant | LOW | c.-20G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | chr3 | 12484878 | ||||||
| chr3:12489922
|
G | A | 2 | a0002a0004 | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
missense_variant | MODERATE | c.122G>A | p.Arg41His | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/12 | 540/2753 | 122/1398 | 41/465 | chr3 | 12489922 | ||
| chr3:12503330
|
G | A | 1 | a0003 | 23 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(20): Show |
missense_variant | MODERATE | c.377G>A | p.Arg126His | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/12 | 795/2753 | 377/1398 | 126/465 | chr3 | 12503330 | ||
| chr3:12503342
|
A | C | 1 | a0004 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.389A>C | p.Lys130Thr | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/12 | 807/2753 | 389/1398 | 130/465 | chr3 | 12503342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:12489866
|
A | C | 1 | a0001c0008 | 2 | HG03139.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.66A>C | p.Pro22Pro | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/12 | 484/2753 | 66/1398 | 22/465 | chr3 | 12489866 | ||
| chr3:12489908
|
A | G | 1 | a0001c0007 | 3 | HG02145.hp1 HG02280.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.108A>G | p.Glu36Glu | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/12 | 526/2753 | 108/1398 | 36/465 | chr3 | 12489908 | ||
| chr3:12489962
|
G | A | 4 | a0002c0003a0002c0004a0002c0006others(1): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
synonymous_variant | LOW | c.162G>A | p.Ala54Ala | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/12 | 580/2753 | 162/1398 | 54/465 | chr3 | 12489962 | ||
| chr3:12503280
|
G | A | 3 | a0002c0004a0002c0006a0004c0009 | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
synonymous_variant | LOW | c.327G>A | p.Glu109Glu | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/12 | 745/2753 | 327/1398 | 109/465 | chr3 | 12503280 | ||
| chr3:12503592
|
T | C | 3 | a0002c0004a0002c0006a0004c0009 | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
synonymous_variant | LOW | c.639T>C | p.Asp213Asp | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/12 | 1057/2753 | 639/1398 | 213/465 | chr3 | 12503592 | ||
| chr3:12505192
|
A | G | 1 | a0001c0012 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.870A>G | p.Pro290Pro | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/12 | 1288/2753 | 870/1398 | 290/465 | chr3 | 12505192 | ||
| chr3:12519061
|
G | A | 3 | a0001c0010a0002c0004a0004c0009 | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
splice_region_variant&synonymous_variant | LOW | c.963G>A | p.Glu321Glu | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/12 | 1381/2753 | 963/1398 | 321/465 | chr3 | 12519061 | ||
| chr3:12532673
|
G | A | 1 | a0001c0005 | 9 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(6): Show |
synonymous_variant | LOW | c.1350G>A | p.Leu450Leu | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 12/12 | 1768/2753 | 1350/1398 | 450/465 | chr3 | 12532673 | ||
| chr3:12532712
|
C | T | 1 | a0001c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1389C>T | p.Asp463Asp | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 12/12 | 1807/2753 | 1389/1398 | 463/465 | chr3 | 12532712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:12484507
|
G | A | 6 | a0001c0001t0013a0001c0005t0003a0001c0011t0003others(3): Show | 34 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-391G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | 5294 | chr3 | 12484507 | |||||
| chr3:12484524
|
G | A | 1 | a0001c0001t0008 | 5 | HG02258.hp2 HG02559.hp2 HG02922.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-374G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | 5277 | chr3 | 12484524 | |||||
| chr3:12484601
|
C | T | 1 | a0001c0001t0011 | 2 | HG01256.hp1 HG01361.hp1 |
5_prime_UTR_variant | MODIFIER | c.-297C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | 5200 | chr3 | 12484601 | |||||
| chr3:12484678
|
G | A | 1 | a0001c0001t0015 | 1 | HG01346.hp1 | 5_prime_UTR_variant | MODIFIER | c.-220G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | 5123 | chr3 | 12484678 | |||||
| chr3:12484689
|
G | T | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(13): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-209G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | 5112 | chr3 | 12484689 | |||||
| chr3:12484698
|
C | T | 1 | a0001c0012t0017 | 1 | NA20905.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-200C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | chr3 | 12484698 | ||||||
| chr3:12484699
|
G | T | 3 | a0002c0004t0007a0002c0004t0009a0004c0009t0009 | 12 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | chr3 | 12484699 | ||||||
| chr3:12484711
|
C | T | 1 | a0003c0002t0014 | 1 | HG02004.hp1 | 5_prime_UTR_variant | MODIFIER | c.-187C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | 5090 | chr3 | 12484711 | |||||
| chr3:12484725
|
C | T | 2 | a0001c0001t0013a0003c0002t0012 | 2 | HG01884.hp2 NA19043.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-173C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/12 | chr3 | 12484725 | ||||||
| chr3:12532799
|
G | A | 1 | a0001c0001t0019 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*78G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 12/12 | 78 | chr3 | 12532799 | |||||
| chr3:12533013
|
G | T | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(11): Show | 137 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*292G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 12/12 | 292 | chr3 | 12533013 | |||||
| chr3:12533398
|
A | G | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(11): Show | 137 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*677A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 12/12 | 677 | chr3 | 12533398 | |||||
| chr3:12533436
|
G | A | 10 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(7): Show | 116 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*715G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 12/12 | 715 | chr3 | 12533436 | |||||
| chr3:12533562
|
A | G | 1 | a0001c0001t0006 | 11 | HG00733.hp1 HG01192.hp2 HG01433.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*841A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 12/12 | 841 | chr3 | 12533562 | |||||
| chr3:12533607
|
C | T | 1 | a0001c0001t0016 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*886C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 12/12 | 886 | chr3 | 12533607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:12484881
|
G | T | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
splice_donor_variant&intron_variant | HIGH | c.-18+1G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12484881 | ||||||
| chr3:12484903
|
G | C | 134 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(131): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-18+23G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12484903 | ||||||
| chr3:12485363
|
C | G | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+483C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485363 | ||||||
| chr3:12485406
|
T | TG | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-18+526_-18+527ins others(1): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485406 | ||||||
| chr3:12485408
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+528G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485408 | ||||||
| chr3:12485434
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-18+554A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485434 | ||||||
| chr3:12485514
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-18+634G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485514 | ||||||
| chr3:12485632
|
C | G | 1 | a0001c0001t0001g0234 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-18+752C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485632 | ||||||
| chr3:12485656
|
G | C | 30 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(27): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+776G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485656 | ||||||
| chr3:12485743
|
C | T | 30 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(27): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+863C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485743 | ||||||
| chr3:12485951
|
AT | A | 30 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(27): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+1072delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485951 | ||||||
| chr3:12485958
|
T | C | 30 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(27): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+1078T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12485958 | ||||||
| chr3:12486050
|
A | T | 11 | a0002c0004t0007g0010a0002c0004t0007g0032a0002c0004t0007g0033others(8): Show | 12 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+1170A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486050 | ||||||
| chr3:12486074
|
G | A | 2 | a0001c0001t0004g0042a0001c0001t0005g0043 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-18+1194G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486074 | ||||||
| chr3:12486101
|
G | T | 25 | a0001c0001t0013g0214a0001c0005t0003g0004a0001c0005t0003g0023others(22): Show | 34 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18+1221G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486101 | ||||||
| chr3:12486441
|
T | A | 30 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(27): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+1561T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486441 | ||||||
| chr3:12486553
|
A | G | 1 | a0001c0001t0010g0212 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-18+1673A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486553 | ||||||
| chr3:12486667
|
A | G | 1 | a0001c0001t0002g0135 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-18+1787A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486667 | ||||||
| chr3:12486691
|
C | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01069.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-18+1811C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486691 | ||||||
| chr3:12486691
|
C | T | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+1811C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486691 | ||||||
| chr3:12486756
|
C | T | 4 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(1): Show | 9 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+1876C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486756 | ||||||
| chr3:12486905
|
G | T | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+2025G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12486905 | ||||||
| chr3:12487084
|
A | G | 101 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(98): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-18+2204A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487084 | ||||||
| chr3:12487204
|
G | C | 30 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(27): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+2324G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487204 | ||||||
| chr3:12487327
|
G | A | 1 | a0001c0007t0004g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18+2447G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487327 | ||||||
| chr3:12487381
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-17-2403T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487381 | ||||||
| chr3:12487502
|
AT | A | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-2275delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 12487502 | |||||
| chr3:12487518
|
G | A | 2 | a0001c0001t0002g0048a0001c0001t0002g0049 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-17-2266G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487518 | ||||||
| chr3:12487553
|
G | GTTA | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-2229_-17-2227d others(5): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 12487553 | |||||
| chr3:12487586
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-17-2198A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487586 | ||||||
| chr3:12487712
|
TTAG | T | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-17-2069_-17-2067d others(5): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 12487712 | |||||
| chr3:12487716
|
T | G | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-17-2068T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487716 | ||||||
| chr3:12487717
|
A | G | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-17-2067A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487717 | ||||||
| chr3:12487760
|
C | T | 1 | a0004c0009t0009g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-17-2024C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487760 | ||||||
| chr3:12487943
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-17-1841A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12487943 | ||||||
| chr3:12487964
|
CA | C | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-1818delA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 12487964 | |||||
| chr3:12488093
|
C | A | 164 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(161): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.-17-1691C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12488093 | ||||||
| chr3:12488102
|
T | C | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-1682T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12488102 | ||||||
| chr3:12488393
|
A | G | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-1391A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12488393 | ||||||
| chr3:12488640
|
T | A | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-17-1144T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12488640 | ||||||
| chr3:12488685
|
G | T | 33 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(30): Show | 37 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.-17-1099G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12488685 | ||||||
| chr3:12488847
|
G | C | 2 | a0001c0001t0013g0214a0003c0002t0012g0213 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-17-937G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12488847 | ||||||
| chr3:12488914
|
T | C | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-870T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12488914 | ||||||
| chr3:12488962
|
A | G | 1 | a0003c0002t0003g0231 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-17-822A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12488962 | ||||||
| chr3:12489047
|
A | G | 2 | a0001c0001t0004g0042a0001c0001t0005g0043 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-17-737A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489047 | ||||||
| chr3:12489061
|
C | T | 3 | a0001c0001t0002g0133a0001c0001t0005g0131a0001c0001t0019g0132 | 3 | HG01993.hp1 NA18948.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-17-723C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489061 | ||||||
| chr3:12489073
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-17-711G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489073 | ||||||
| chr3:12489168
|
CT | C | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-613delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 12489168 | |||||
| chr3:12489258
|
C | T | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-526C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489258 | ||||||
| chr3:12489286
|
A | G | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-498A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489286 | ||||||
| chr3:12489302
|
G | GT | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-481dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 12489302 | |||||
| chr3:12489329
|
C | T | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-17-455C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489329 | ||||||
| chr3:12489526
|
G | A | 2 | a0001c0001t0004g0052a0001c0001t0004g0053 | 2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-17-258G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489526 | ||||||
| chr3:12489566
|
G | T | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-218G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489566 | ||||||
| chr3:12489645
|
A | G | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-17-139A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489645 | ||||||
| chr3:12489654
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-17-130C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489654 | ||||||
| chr3:12489666
|
T | A | 34 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(31): Show | 38 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-118T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489666 | ||||||
| chr3:12489669
|
A | G | 2 | a0003c0002t0003g0230a0003c0002t0003g0231 | 2 | HG01993.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-17-115A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 1/11 | chr3 | 12489669 | ||||||
| chr3:12490082
|
A | G | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+93A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490082 | ||||||
| chr3:12490105
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.189+116C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490105 | ||||||
| chr3:12490248
|
A | AT | 28 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(25): Show | 31 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.189+267dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 12490248 | |||||
| chr3:12490326
|
G | A | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+337G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490326 | ||||||
| chr3:12490403
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.189+414A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490403 | ||||||
| chr3:12490429
|
A | G | 28 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(25): Show | 31 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.189+440A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490429 | ||||||
| chr3:12490437
|
C | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0210 | 6 | HG01346.hp2 HG01943.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+448C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490437 | ||||||
| chr3:12490551
|
A | T | 28 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(25): Show | 31 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.189+562A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490551 | ||||||
| chr3:12490558
|
A | G | 111 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.189+569A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490558 | ||||||
| chr3:12490609
|
T | A | 28 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(25): Show | 31 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.189+620T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490609 | ||||||
| chr3:12490737
|
GC | G | 3 | a0003c0002t0003g0215a0003c0002t0003g0216a0003c0002t0003g0217 | 3 | HG00423.hp1 NA18981.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.189+751delC | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 12490737 | |||||
| chr3:12490769
|
G | A | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.189+780G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490769 | ||||||
| chr3:12490829
|
G | T | 25 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(22): Show | 28 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.189+840G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12490829 | ||||||
| chr3:12490989
|
GT | G | 133 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(130): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.189+1008delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 12490989 | |||||
| chr3:12491001
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.189+1012T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491001 | ||||||
| chr3:12491002
|
G | GT | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.189+1019dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 12491002 | |||||
| chr3:12491015
|
G | C | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+1026G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491015 | ||||||
| chr3:12491116
|
G | A | 1 | a0001c0001t0010g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.190-1020G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491116 | ||||||
| chr3:12491462
|
G | A | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.190-674G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491462 | ||||||
| chr3:12491508
|
C | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-628C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491508 | ||||||
| chr3:12491517
|
C | T | 1 | a0001c0007t0004g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.190-619C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491517 | ||||||
| chr3:12491649
|
G | T | 18 | a0003c0002t0003g0006a0003c0002t0003g0022a0003c0002t0003g0215others(15): Show | 22 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.190-487G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491649 | ||||||
| chr3:12491765
|
T | C | 4 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(1): Show | 9 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-371T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491765 | ||||||
| chr3:12491776
|
T | C | 1 | a0001c0001t0004g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-360T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491776 | ||||||
| chr3:12491836
|
A | C | 109 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.190-300A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12491836 | ||||||
| chr3:12492006
|
C | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-130C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12492006 | ||||||
| chr3:12492079
|
C | T | 13 | a0001c0001t0002g0123a0001c0001t0002g0127a0001c0001t0006g0115others(10): Show | 13 | HG00733.hp1 HG01192.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.190-57C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 2/11 | chr3 | 12492079 | ||||||
| chr3:12492254
|
TA | T | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.271+39delA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12492254 | |||||
| chr3:12492653
|
T | A | 4 | a0001c0001t0004g0045a0001c0007t0004g0044a0001c0007t0004g0046others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+436T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12492653 | ||||||
| chr3:12492702
|
T | A | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.271+485T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12492702 | ||||||
| chr3:12492799
|
C | T | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.271+582C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12492799 | ||||||
| chr3:12492828
|
C | T | 109 | a0001c0001t0001g0209a0001c0001t0002g0002a0001c0001t0002g0011others(106): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.271+611C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12492828 | ||||||
| chr3:12492840
|
T | G | 1 | a0003c0002t0003g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.271+623T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12492840 | ||||||
| chr3:12493132
|
ATAT | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.271+917_271+919del others(3): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12493132 | |||||
| chr3:12493147
|
G | C | 3 | a0001c0007t0004g0044a0001c0007t0004g0046a0001c0007t0004g0047 | 3 | HG02145.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.271+930G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12493147 | ||||||
| chr3:12493360
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.271+1143G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12493360 | ||||||
| chr3:12493424
|
A | G | 109 | a0001c0001t0001g0209a0001c0001t0002g0002a0001c0001t0002g0011others(106): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.271+1207A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12493424 | ||||||
| chr3:12493456
|
C | T | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.271+1239C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12493456 | ||||||
| chr3:12493500
|
G | A | 1 | a0001c0001t0016g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.271+1283G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12493500 | ||||||
| chr3:12493550
|
A | C | 1 | a0001c0001t0005g0114 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.271+1333A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12493550 | ||||||
| chr3:12494120
|
G | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.271+1903G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494120 | ||||||
| chr3:12494141
|
A | C | 1 | a0003c0002t0003g0230 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.271+1924A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494141 | ||||||
| chr3:12494230
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.271+2013C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494230 | ||||||
| chr3:12494240
|
T | C | 110 | a0001c0001t0001g0209a0001c0001t0002g0002a0001c0001t0002g0011others(107): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.271+2023T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494240 | ||||||
| chr3:12494252
|
AT | A | 110 | a0001c0001t0001g0209a0001c0001t0002g0002a0001c0001t0002g0011others(107): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.271+2036delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494252 | ||||||
| chr3:12494264
|
C | T | 1 | a0001c0007t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.271+2047C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494264 | ||||||
| chr3:12494282
|
A | G | 1 | a0003c0002t0003g0217 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.271+2065A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494282 | ||||||
| chr3:12494292
|
G | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.271+2075G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494292 | ||||||
| chr3:12494386
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.272-2132A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494386 | ||||||
| chr3:12494492
|
G | A | 2 | a0001c0001t0013g0214a0003c0002t0012g0213 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.272-2026G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494492 | ||||||
| chr3:12494523
|
G | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.272-1995G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494523 | ||||||
| chr3:12494536
|
G | C | 2 | a0002c0004t0007g0032a0002c0004t0007g0033 | 2 | HG02129.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.272-1982G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494536 | ||||||
| chr3:12494608
|
G | C | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.272-1910G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494608 | ||||||
| chr3:12494644
|
G | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01168.hp1 HG01169.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.272-1874G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494644 | ||||||
| chr3:12494662
|
A | G | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.272-1856A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494662 | ||||||
| chr3:12494681
|
A | G | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.272-1837A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494681 | ||||||
| chr3:12494698
|
A | ACCAATTT others(305): Show |
11 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(8): Show | 12 | HG01934.hp1 HG02004.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.272-1808_272-1807i others(314): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12494698 | |||||
| chr3:12494698
|
A | ACCAATTT others(306): Show |
4 | a0002c0004t0007g0037a0002c0004t0007g0038a0002c0004t0007g0039others(1): Show | 4 | HG01243.hp2 HG01928.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-1808_272-1807i others(315): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12494698 | |||||
| chr3:12494823
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.272-1695A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494823 | ||||||
| chr3:12494875
|
C | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.272-1643C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494875 | ||||||
| chr3:12494955
|
G | A | 4 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(1): Show | 9 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.272-1563G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494955 | ||||||
| chr3:12494973
|
A | G | 1 | a0001c0001t0004g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.272-1545A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12494973 | ||||||
| chr3:12495126
|
C | CA | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG02055.hp2 HG03195.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-1370dupA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12495126 | |||||
| chr3:12495126
|
C | CAAA | 19 | a0001c0001t0002g0055a0001c0001t0002g0106a0001c0001t0002g0107others(16): Show | 23 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.272-1372_272-1370d others(5): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12495126 | |||||
| chr3:12495126
|
C | CAAAA | 93 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(90): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.272-1373_272-1370d others(6): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12495126 | |||||
| chr3:12495126
|
C | CAAAAA | 17 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059others(14): Show | 17 | HG00733.hp1 HG01192.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.272-1374_272-1370d others(7): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12495126 | |||||
| chr3:12495126
|
CA | C | 6 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 6 | HG01070.hp2 HG02300.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-1370delA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 12495126 | |||||
| chr3:12495452
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.272-1066A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12495452 | ||||||
| chr3:12495489
|
G | C | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.272-1029G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12495489 | ||||||
| chr3:12495541
|
C | T | 16 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0048others(13): Show | 23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.272-977C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12495541 | ||||||
| chr3:12495752
|
A | T | 1 | a0001c0007t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.272-766A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12495752 | ||||||
| chr3:12495818
|
C | T | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.272-700C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12495818 | ||||||
| chr3:12495970
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.272-548G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12495970 | ||||||
| chr3:12496023
|
C | T | 2 | a0001c0001t0004g0052a0001c0001t0004g0053 | 2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.272-495C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496023 | ||||||
| chr3:12496119
|
A | G | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.272-399A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496119 | ||||||
| chr3:12496130
|
G | A | 2 | a0001c0001t0004g0068a0001c0001t0004g0069 | 2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.272-388G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496130 | ||||||
| chr3:12496140
|
A | T | 1 | a0002c0004t0009g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.272-378A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496140 | ||||||
| chr3:12496203
|
G | A | 1 | a0001c0001t0006g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.272-315G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496203 | ||||||
| chr3:12496255
|
A | G | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.272-263A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496255 | ||||||
| chr3:12496425
|
T | C | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.272-93T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496425 | ||||||
| chr3:12496446
|
T | C | 1 | a0001c0007t0004g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.272-72T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496446 | ||||||
| chr3:12496456
|
T | A | 107 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(104): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.272-62T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496456 | ||||||
| chr3:12496514
|
C | G | 1 | a0001c0001t0016g0155 | 1 | HG00323.hp2 | splice_region_variant&intron_variant | LOW | c.272-4C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 3/11 | chr3 | 12496514 | ||||||
| chr3:12496612
|
A | G | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.308+58A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12496612 | ||||||
| chr3:12496752
|
T | G | 4 | a0001c0001t0004g0045a0001c0007t0004g0044a0001c0007t0004g0046others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.308+198T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12496752 | ||||||
| chr3:12496778
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.308+224A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12496778 | ||||||
| chr3:12496870
|
G | T | 1 | a0001c0001t0001g0197 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.308+316G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12496870 | ||||||
| chr3:12496894
|
C | G | 1 | a0001c0007t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.308+340C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12496894 | ||||||
| chr3:12497005
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.308+451A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497005 | ||||||
| chr3:12497048
|
C | T | 2 | a0002c0006t0005g0237a0002c0006t0005g0238 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.308+494C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497048 | ||||||
| chr3:12497096
|
T | C | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.308+542T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497096 | ||||||
| chr3:12497162
|
G | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308+608G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497162 | ||||||
| chr3:12497220
|
T | C | 141 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(138): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.308+666T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497220 | ||||||
| chr3:12497278
|
C | T | 1 | a0002c0003t0004g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.308+724C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497278 | ||||||
| chr3:12497309
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.308+755A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497309 | ||||||
| chr3:12497372
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.308+818G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497372 | ||||||
| chr3:12497426
|
C | T | 3 | a0003c0002t0003g0229a0003c0002t0003g0230a0003c0002t0003g0231 | 3 | HG00099.hp1 HG01993.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.308+872C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497426 | ||||||
| chr3:12497427
|
G | A | 108 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(105): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.308+873G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497427 | ||||||
| chr3:12497520
|
G | A | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.308+966G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497520 | ||||||
| chr3:12497680
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.308+1126G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497680 | ||||||
| chr3:12497739
|
T | C | 26 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(23): Show | 29 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.308+1185T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497739 | ||||||
| chr3:12497757
|
C | G | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.308+1203C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497757 | ||||||
| chr3:12497818
|
A | G | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.308+1264A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497818 | ||||||
| chr3:12497912
|
G | A | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.308+1358G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12497912 | ||||||
| chr3:12498070
|
CT | C | 11 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(8): Show | 13 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.308+1528delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 12498070 | |||||
| chr3:12498123
|
G | A | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.308+1569G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498123 | ||||||
| chr3:12498233
|
C | T | 1 | a0001c0001t0006g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.308+1679C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498233 | ||||||
| chr3:12498287
|
G | T | 1 | a0001c0001t0004g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.308+1733G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498287 | ||||||
| chr3:12498298
|
G | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308+1744G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498298 | ||||||
| chr3:12498338
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308+1784A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498338 | ||||||
| chr3:12498473
|
C | T | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308+1919C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498473 | ||||||
| chr3:12498541
|
C | T | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.308+1987C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498541 | ||||||
| chr3:12498628
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.308+2074C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498628 | ||||||
| chr3:12498699
|
A | G | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.308+2145A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498699 | ||||||
| chr3:12498861
|
A | G | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.308+2307A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498861 | ||||||
| chr3:12498956
|
G | C | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.308+2402G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498956 | ||||||
| chr3:12498970
|
G | C | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.308+2416G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12498970 | ||||||
| chr3:12499253
|
G | C | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.308+2699G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499253 | ||||||
| chr3:12499359
|
G | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308+2805G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499359 | ||||||
| chr3:12499384
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.308+2830T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499384 | ||||||
| chr3:12499474
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0195 | 3 | HG02257.hp2 HG02486.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.308+2920A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499474 | ||||||
| chr3:12499592
|
T | C | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308+3038T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499592 | ||||||
| chr3:12499597
|
C | A | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.308+3043C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499597 | ||||||
| chr3:12499766
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308+3212A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499766 | ||||||
| chr3:12499820
|
T | G | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.308+3266T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499820 | ||||||
| chr3:12499883
|
A | G | 3 | a0001c0001t0002g0013a0001c0001t0002g0076a0001c0001t0002g0077 | 4 | HG00099.hp2 HG01074.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+3329A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499883 | ||||||
| chr3:12499940
|
G | T | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-3322G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499940 | ||||||
| chr3:12499944
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.309-3318C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499944 | ||||||
| chr3:12499949
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.309-3313A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499949 | ||||||
| chr3:12499964
|
G | T | 2 | a0001c0001t0004g0042a0001c0001t0005g0043 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.309-3298G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12499964 | ||||||
| chr3:12500077
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0193 | 2 | HG00558.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.309-3185C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500077 | ||||||
| chr3:12500294
|
T | C | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.309-2968T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500294 | ||||||
| chr3:12500444
|
G | GA | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-2818_309-2817i others(3): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500444 | ||||||
| chr3:12500531
|
A | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.309-2731A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500531 | ||||||
| chr3:12500563
|
A | C | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.309-2699A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500563 | ||||||
| chr3:12500803
|
G | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-2459G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500803 | ||||||
| chr3:12500859
|
T | A | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.309-2403T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500859 | ||||||
| chr3:12500952
|
G | T | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-2310G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500952 | ||||||
| chr3:12500970
|
C | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-2292C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12500970 | ||||||
| chr3:12501026
|
T | C | 1 | a0001c0007t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.309-2236T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501026 | ||||||
| chr3:12501049
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.309-2213T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501049 | ||||||
| chr3:12501175
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-2087A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501175 | ||||||
| chr3:12501366
|
G | A | 2 | a0001c0001t0005g0131a0001c0001t0019g0132 | 2 | HG01993.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.309-1896G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501366 | ||||||
| chr3:12501384
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-1878A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501384 | ||||||
| chr3:12501431
|
C | T | 1 | a0001c0001t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.309-1831C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501431 | ||||||
| chr3:12501434
|
G | A | 2 | a0001c0001t0002g0048a0001c0001t0002g0049 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.309-1828G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501434 | ||||||
| chr3:12501487
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-1775A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501487 | ||||||
| chr3:12501614
|
C | CT | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.309-1637dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 12501614 | |||||
| chr3:12501614
|
CT | C | 2 | a0001c0005t0003g0004a0001c0005t0003g0232 | 6 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.309-1637delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 12501614 | |||||
| chr3:12501659
|
T | C | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-1603T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501659 | ||||||
| chr3:12501664
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-1598A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501664 | ||||||
| chr3:12501699
|
G | A | 19 | a0003c0002t0003g0006a0003c0002t0003g0022a0003c0002t0003g0215others(16): Show | 23 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.309-1563G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501699 | ||||||
| chr3:12501772
|
C | T | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-1490C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501772 | ||||||
| chr3:12501799
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-1463A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501799 | ||||||
| chr3:12501976
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-1286A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12501976 | ||||||
| chr3:12502033
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0194 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.309-1229A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502033 | ||||||
| chr3:12502095
|
A | G | 6 | a0003c0002t0003g0006a0003c0002t0003g0022a0003c0002t0003g0219others(3): Show | 10 | HG00639.hp2 HG01099.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.309-1167A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502095 | ||||||
| chr3:12502274
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.309-988G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502274 | ||||||
| chr3:12502317
|
G | A | 2 | a0001c0001t0004g0068a0001c0001t0004g0069 | 2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.309-945G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502317 | ||||||
| chr3:12502319
|
T | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-943T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502319 | ||||||
| chr3:12502320
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.309-942C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502320 | ||||||
| chr3:12502369
|
G | A | 2 | a0001c0001t0004g0042a0001c0001t0005g0043 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.309-893G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502369 | ||||||
| chr3:12502598
|
T | G | 1 | a0001c0001t0004g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309-664T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502598 | ||||||
| chr3:12502659
|
TGG | T | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.309-599_309-598del others(2): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 12502659 | |||||
| chr3:12502662
|
G | A | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.309-600G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502662 | ||||||
| chr3:12502663
|
G | T | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.309-599G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502663 | ||||||
| chr3:12502677
|
G | GT | 8 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(5): Show | 8 | HG01070.hp2 HG02135.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.309-574dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 12502677 | |||||
| chr3:12502689
|
G | GT | 28 | a0001c0001t0001g0158a0001c0001t0004g0042a0001c0001t0013g0214others(25): Show | 37 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.309-561dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 12502689 | |||||
| chr3:12502689
|
G | T | 1 | a0001c0001t0005g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.309-573G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502689 | ||||||
| chr3:12502689
|
GT | G | 13 | a0001c0007t0004g0044a0001c0007t0004g0046a0001c0007t0004g0047others(10): Show | 15 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.309-561delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 12502689 | |||||
| chr3:12502690
|
T | TTTTTTTT others(4): Show |
18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-562_309-561ins others(11): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 12502690 | |||||
| chr3:12502720
|
T | A | 1 | a0003c0002t0003g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.309-542T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502720 | ||||||
| chr3:12502876
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-386A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502876 | ||||||
| chr3:12502910
|
A | G | 1 | a0001c0011t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.309-352A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502910 | ||||||
| chr3:12502924
|
T | C | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-338T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12502924 | ||||||
| chr3:12503082
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.309-180A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 4/11 | chr3 | 12503082 | ||||||
| chr3:12503994
|
A | G | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.831+210A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/11 | chr3 | 12503994 | ||||||
| chr3:12504105
|
A | G | 3 | a0003c0002t0003g0229a0003c0002t0003g0230a0003c0002t0003g0231 | 3 | HG00099.hp1 HG01993.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.831+321A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/11 | chr3 | 12504105 | ||||||
| chr3:12504318
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.831+534A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/11 | chr3 | 12504318 | ||||||
| chr3:12504446
|
G | A | 1 | a0003c0002t0003g0226 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.831+662G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/11 | chr3 | 12504446 | ||||||
| chr3:12504563
|
G | A | 18 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(15): Show | 19 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.832-591G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/11 | chr3 | 12504563 | ||||||
| chr3:12504654
|
A | G | 1 | a0001c0005t0003g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.832-500A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/11 | chr3 | 12504654 | ||||||
| chr3:12504673
|
T | G | 94 | a0001c0001t0001g0210a0001c0001t0002g0002a0001c0001t0002g0011others(91): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.832-481T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/11 | chr3 | 12504673 | ||||||
| chr3:12505024
|
C | A | 1 | a0001c0001t0001g0017 | 2 | NA18981.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.832-130C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 5/11 | chr3 | 12505024 | ||||||
| chr3:12505246
|
T | C | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.909+15T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505246 | ||||||
| chr3:12505265
|
G | A | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+34G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505265 | ||||||
| chr3:12505320
|
A | G | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.909+89A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505320 | ||||||
| chr3:12505648
|
A | G | 166 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.909+417A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505648 | ||||||
| chr3:12505661
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0059a0001c0001t0002g0078 | 4 | HG01070.hp1 HG01071.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+430G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505661 | ||||||
| chr3:12505708
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.909+477C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505708 | ||||||
| chr3:12505709
|
G | A | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+478G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505709 | ||||||
| chr3:12505783
|
C | CA | 114 | a0001c0001t0001g0161a0001c0001t0001g0164a0001c0001t0001g0165others(111): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.909+573dupA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12505783 | |||||
| chr3:12505783
|
C | CAA | 9 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 11 | HG01175.hp1 HG02280.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+572_909+573dup others(2): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12505783 | |||||
| chr3:12505783
|
CAA | C | 14 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(11): Show | 15 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.909+572_909+573del others(2): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12505783 | |||||
| chr3:12505900
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0166 | 3 | HG01069.hp2 HG01358.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.909+669G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505900 | ||||||
| chr3:12505930
|
G | A | 1 | a0002c0004t0007g0032 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.909+699G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12505930 | ||||||
| chr3:12506013
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.909+782T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506013 | ||||||
| chr3:12506020
|
G | A | 1 | a0001c0011t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.909+789G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506020 | ||||||
| chr3:12506108
|
ATACTATA others(71): Show |
A | 11 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(8): Show | 13 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.909+882_909+959del others(78): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12506108 | |||||
| chr3:12506158
|
G | A | 114 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(111): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.909+927G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506158 | ||||||
| chr3:12506163
|
T | A | 1 | a0001c0001t0010g0212 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.909+932T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506163 | ||||||
| chr3:12506277
|
C | G | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.909+1046C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506277 | ||||||
| chr3:12506344
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.909+1113C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506344 | ||||||
| chr3:12506424
|
A | C | 13 | a0001c0001t0002g0123a0001c0001t0002g0127a0001c0001t0006g0115others(10): Show | 13 | HG00733.hp1 HG01192.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+1193A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506424 | ||||||
| chr3:12506578
|
C | CA | 8 | a0001c0001t0002g0076a0001c0001t0002g0130a0001c0001t0004g0045others(5): Show | 8 | HG00099.hp2 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1364dupA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12506578 | |||||
| chr3:12506578
|
CA | C | 21 | a0001c0001t0001g0153a0001c0001t0001g0189a0001c0001t0001g0207others(18): Show | 23 | HG01074.hp2 HG01099.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+1364delA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12506578 | |||||
| chr3:12506743
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.909+1512G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506743 | ||||||
| chr3:12506762
|
C | T | 1 | a0002c0004t0001g0149 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.909+1531C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12506762 | ||||||
| chr3:12507337
|
C | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG01934.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.909+2106C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12507337 | ||||||
| chr3:12507444
|
G | C | 94 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(91): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.909+2213G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12507444 | ||||||
| chr3:12507788
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.909+2557A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12507788 | ||||||
| chr3:12507812
|
T | C | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+2581T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12507812 | ||||||
| chr3:12507982
|
G | A | 4 | a0001c0001t0002g0055a0001c0001t0002g0106a0001c0001t0002g0107others(1): Show | 4 | NA18969.hp1 NA18971.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+2751G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12507982 | ||||||
| chr3:12508001
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.909+2770G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508001 | ||||||
| chr3:12508061
|
C | T | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.909+2830C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508061 | ||||||
| chr3:12508266
|
C | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.909+3035C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508266 | ||||||
| chr3:12508397
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.909+3166C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508397 | ||||||
| chr3:12508511
|
G | A | 1 | a0002c0004t0001g0147 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.909+3280G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508511 | ||||||
| chr3:12508565
|
G | A | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.909+3334G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508565 | ||||||
| chr3:12508579
|
A | G | 166 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.909+3348A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508579 | ||||||
| chr3:12508649
|
G | A | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.909+3418G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508649 | ||||||
| chr3:12508663
|
G | A | 1 | a0001c0007t0004g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.909+3432G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508663 | ||||||
| chr3:12508700
|
A | G | 24 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(21): Show | 33 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.909+3469A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508700 | ||||||
| chr3:12508736
|
A | G | 113 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.909+3505A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508736 | ||||||
| chr3:12508811
|
A | G | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.909+3580A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12508811 | ||||||
| chr3:12509010
|
G | A | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+3779G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509010 | ||||||
| chr3:12509182
|
G | T | 18 | a0001c0001t0006g0115a0001c0001t0006g0116a0001c0010t0001g0151others(15): Show | 19 | HG00733.hp1 HG01192.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.909+3951G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509182 | ||||||
| chr3:12509192
|
G | GT | 16 | a0001c0001t0006g0124a0001c0010t0001g0151a0002c0004t0001g0147others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.909+3969dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12509192 | |||||
| chr3:12509194
|
T | A | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+3963T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509194 | ||||||
| chr3:12509201
|
G | T | 14 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(11): Show | 15 | HG01243.hp2 HG01928.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.909+3970G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509201 | ||||||
| chr3:12509207
|
G | GT | 116 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(113): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.909+3987dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12509207 | |||||
| chr3:12509210
|
T | G | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.909+3979T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509210 | ||||||
| chr3:12509213
|
T | G | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.909+3982T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509213 | ||||||
| chr3:12509265
|
A | G | 5 | a0002c0004t0007g0010a0002c0004t0007g0035a0002c0004t0007g0037others(2): Show | 6 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+4034A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509265 | ||||||
| chr3:12509281
|
A | G | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+4050A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509281 | ||||||
| chr3:12509296
|
G | T | 1 | a0003c0002t0012g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.909+4065G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509296 | ||||||
| chr3:12509379
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.909+4148T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509379 | ||||||
| chr3:12509435
|
A | G | 94 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(91): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.909+4204A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509435 | ||||||
| chr3:12509480
|
A | T | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.909+4249A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509480 | ||||||
| chr3:12509494
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.909+4263G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509494 | ||||||
| chr3:12509558
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.909+4327T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509558 | ||||||
| chr3:12509666
|
C | G | 1 | a0001c0001t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.909+4435C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509666 | ||||||
| chr3:12509767
|
G | A | 4 | a0001c0001t0002g0055a0001c0001t0002g0106a0001c0001t0002g0107others(1): Show | 4 | NA18969.hp1 NA18971.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+4536G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509767 | ||||||
| chr3:12509772
|
A | G | 1 | a0003c0002t0012g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.909+4541A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509772 | ||||||
| chr3:12509952
|
A | C | 1 | a0001c0001t0006g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+4721A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509952 | ||||||
| chr3:12509992
|
C | A | 1 | a0002c0004t0001g0148 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.909+4761C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509992 | ||||||
| chr3:12509992
|
C | G | 109 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.909+4761C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12509992 | ||||||
| chr3:12510016
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.909+4785G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510016 | ||||||
| chr3:12510060
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.909+4829T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510060 | ||||||
| chr3:12510253
|
C | T | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+5022C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510253 | ||||||
| chr3:12510308
|
T | C | 24 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(21): Show | 33 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.909+5077T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510308 | ||||||
| chr3:12510321
|
A | G | 3 | a0002c0006t0005g0236a0002c0006t0005g0237a0002c0006t0005g0238 | 3 | HG02572.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.909+5090A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510321 | ||||||
| chr3:12510333
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.909+5102T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510333 | ||||||
| chr3:12510382
|
T | G | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.909+5151T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510382 | ||||||
| chr3:12510554
|
C | T | 1 | a0001c0001t0002g0080 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.909+5323C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510554 | ||||||
| chr3:12510585
|
A | G | 166 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.909+5354A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510585 | ||||||
| chr3:12510587
|
A | G | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG02040.hp1 NA18966.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.909+5356A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510587 | ||||||
| chr3:12510664
|
G | A | 2 | a0001c0001t0004g0042a0001c0001t0005g0043 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.909+5433G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510664 | ||||||
| chr3:12510717
|
C | CT | 4 | a0001c0001t0001g0146a0001c0001t0001g0197a0001c0001t0011g0184others(1): Show | 4 | HG00673.hp1 HG01256.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+5487dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12510717 | |||||
| chr3:12510816
|
A | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163 | 5 | NA18939.hp1 NA18969.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+5585A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510816 | ||||||
| chr3:12510927
|
A | T | 1 | a0002c0004t0001g0148 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.910-5684A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12510927 | ||||||
| chr3:12511007
|
A | G | 129 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.910-5604A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12511007 | ||||||
| chr3:12511129
|
A | C | 129 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.910-5482A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12511129 | ||||||
| chr3:12511460
|
T | C | 1 | a0004c0009t0009g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.910-5151T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12511460 | ||||||
| chr3:12511481
|
A | C | 24 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(21): Show | 33 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.910-5130A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12511481 | ||||||
| chr3:12511569
|
C | CT | 133 | a0001c0001t0001g0183a0001c0001t0001g0195a0001c0001t0002g0002others(130): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.910-5027dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12511569 | |||||
| chr3:12511569
|
C | CTT | 23 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0059others(20): Show | 26 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-5028_910-5027d others(4): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12511569 | |||||
| chr3:12511826
|
G | C | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.910-4785G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12511826 | ||||||
| chr3:12512364
|
C | A | 1 | a0001c0001t0002g0082 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.910-4247C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12512364 | ||||||
| chr3:12512434
|
C | T | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.910-4177C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12512434 | ||||||
| chr3:12512570
|
A | G | 139 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(136): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.910-4041A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12512570 | ||||||
| chr3:12512806
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.910-3805G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12512806 | ||||||
| chr3:12512948
|
T | C | 1 | a0001c0001t0010g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.910-3663T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12512948 | ||||||
| chr3:12512971
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.910-3640G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12512971 | ||||||
| chr3:12513129
|
T | G | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-3482T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513129 | ||||||
| chr3:12513269
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.910-3342T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513269 | ||||||
| chr3:12513334
|
A | G | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-3277A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513334 | ||||||
| chr3:12513410
|
G | A | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-3201G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513410 | ||||||
| chr3:12513491
|
C | T | 1 | a0001c0001t0004g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.910-3120C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513491 | ||||||
| chr3:12513504
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.910-3107T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513504 | ||||||
| chr3:12513650
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.910-2961G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513650 | ||||||
| chr3:12513806
|
G | A | 1 | a0001c0011t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.910-2805G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513806 | ||||||
| chr3:12513867
|
G | A | 1 | a0001c0001t0013g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.910-2744G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513867 | ||||||
| chr3:12513929
|
C | T | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-2682C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12513929 | ||||||
| chr3:12514025
|
T | C | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-2586T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12514025 | ||||||
| chr3:12514045
|
G | A | 3 | a0001c0007t0004g0044a0001c0007t0004g0046a0001c0007t0004g0047 | 3 | HG02145.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.910-2566G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12514045 | ||||||
| chr3:12514081
|
G | A | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-2530G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12514081 | ||||||
| chr3:12514481
|
G | T | 1 | a0002c0003t0002g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.910-2130G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12514481 | ||||||
| chr3:12514876
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.910-1735A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12514876 | ||||||
| chr3:12514889
|
A | T | 4 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(1): Show | 9 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-1722A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12514889 | ||||||
| chr3:12514971
|
ATCTGCTT others(8): Show |
A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.910-1639_910-1625d others(17): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12514971 | ||||||
| chr3:12515008
|
T | A | 112 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(109): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.910-1603T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12515008 | ||||||
| chr3:12515112
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.910-1499A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12515112 | ||||||
| chr3:12515388
|
C | T | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.910-1223C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12515388 | ||||||
| chr3:12515453
|
A | G | 4 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0102others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-1158A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12515453 | ||||||
| chr3:12515692
|
A | G | 1 | a0001c0001t0004g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.910-919A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12515692 | ||||||
| chr3:12515872
|
CT | C | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-729delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12515872 | |||||
| chr3:12515984
|
C | T | 1 | a0003c0002t0003g0228 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.910-627C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12515984 | ||||||
| chr3:12516195
|
C | T | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-416C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516195 | ||||||
| chr3:12516242
|
G | A | 2 | a0001c0007t0004g0044a0001c0007t0004g0046 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.910-369G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516242 | ||||||
| chr3:12516295
|
G | A | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-316G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516295 | ||||||
| chr3:12516432
|
A | G | 2 | a0001c0001t0002g0064a0001c0001t0002g0079 | 2 | HG01175.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.910-179A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516432 | ||||||
| chr3:12516437
|
ACAAAAT | A | 9 | a0001c0001t0002g0055a0001c0001t0002g0057a0001c0001t0002g0070others(6): Show | 9 | NA18939.hp2 NA18949.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-173_910-168del others(6): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516437 | ||||||
| chr3:12516437
|
ACAAAATA others(1): Show |
A | 6 | a0001c0001t0001g0158a0001c0001t0002g0013a0001c0001t0002g0076others(3): Show | 7 | HG00099.hp2 HG01074.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-173_910-166del others(8): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516437 | ||||||
| chr3:12516437
|
ACAAAATA others(3): Show |
A | 12 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0050others(9): Show | 14 | HG00642.hp1 HG01123.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.910-173_910-164del others(10): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516437 | ||||||
| chr3:12516441
|
AAT | A | 11 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0066others(8): Show | 18 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.910-165_910-164del others(2): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516441 | |||||
| chr3:12516441
|
AATAT | A | 13 | a0001c0001t0002g0021a0001c0001t0002g0067a0001c0001t0002g0095others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-167_910-164del others(4): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516441 | |||||
| chr3:12516442
|
A | ATG | 7 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0103others(4): Show | 7 | HG01081.hp2 HG01123.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-168_910-167ins others(2): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516442 | |||||
| chr3:12516442
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0010g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.910-168_910-167ins others(10): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516442 | |||||
| chr3:12516442
|
ATATATG | A | 26 | a0001c0001t0002g0014a0001c0001t0002g0059a0001c0001t0002g0060others(23): Show | 27 | HG00280.hp1 HG00639.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.910-167_910-162del others(6): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516442 | |||||
| chr3:12516442
|
ATATATGT others(1): Show |
A | 4 | a0001c0001t0002g0063a0001c0001t0002g0082a0001c0001t0002g0113others(1): Show | 4 | HG02922.hp1 HG03471.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-167_910-160del others(8): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516442 | |||||
| chr3:12516442
|
ATATATGT others(3): Show |
A | 12 | a0001c0001t0002g0062a0001c0001t0002g0064a0001c0001t0002g0079others(9): Show | 13 | HG01081.hp1 HG01175.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.910-167_910-158del others(10): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516442 | |||||
| chr3:12516442
|
ATATATGT others(5): Show |
A | 1 | a0001c0001t0002g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.910-167_910-156del others(12): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516442 | |||||
| chr3:12516444
|
A | ATGTGTGT others(3): Show |
1 | a0001c0007t0004g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.910-166_910-165ins others(10): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516444 | |||||
| chr3:12516444
|
A | G | 17 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0065others(14): Show | 17 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.910-167A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516444 | ||||||
| chr3:12516444
|
ATATGTGT others(3): Show |
A | 1 | a0001c0007t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.910-165_910-156del others(10): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516444 | |||||
| chr3:12516446
|
A | G | 38 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0048others(35): Show | 45 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.910-165A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516446 | ||||||
| chr3:12516446
|
ATG | A | 15 | a0001c0001t0001g0144a0001c0001t0001g0159a0001c0001t0001g0166others(12): Show | 16 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.910-124_910-123del others(2): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516446 | |||||
| chr3:12516446
|
ATGTG | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(53): Show | 75 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.910-126_910-123del others(4): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516446 | |||||
| chr3:12516446
|
ATGTGTG | A | 4 | a0001c0001t0001g0018a0001c0010t0001g0151a0003c0002t0003g0220others(1): Show | 5 | HG01516.hp2 HG01517.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-128_910-123del others(6): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516446 | |||||
| chr3:12516446
|
ATGTGTGT others(1): Show |
A | 16 | a0001c0001t0001g0186a0001c0011t0003g0218a0002c0003t0002g0008others(13): Show | 18 | HG01074.hp2 HG01099.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.910-130_910-123del others(8): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516446 | |||||
| chr3:12516446
|
ATGTGTGT others(3): Show |
A | 15 | a0003c0002t0003g0006a0003c0002t0003g0022a0003c0002t0003g0215others(12): Show | 19 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.910-132_910-123del others(10): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516446 | |||||
| chr3:12516446
|
ATGTGTGT others(9): Show |
A | 14 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(11): Show | 15 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.910-138_910-123del others(16): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 12516446 | |||||
| chr3:12516448
|
G | A | 13 | a0001c0001t0001g0158a0001c0001t0002g0011a0001c0001t0002g0012others(10): Show | 15 | HG00642.hp1 HG01123.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.910-163G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516448 | ||||||
| chr3:12516454
|
G | A | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.910-157G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516454 | ||||||
| chr3:12516464
|
G | A | 14 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(11): Show | 15 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.910-147G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516464 | ||||||
| chr3:12516569
|
A | G | 15 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.910-42A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 6/11 | chr3 | 12516569 | ||||||
| chr3:12516718
|
G | A | 2 | a0001c0007t0004g0044a0001c0007t0004g0046 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.960+57G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12516718 | ||||||
| chr3:12516898
|
C | A | 1 | a0001c0001t0002g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.960+237C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12516898 | ||||||
| chr3:12517297
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.960+636G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517297 | ||||||
| chr3:12517344
|
C | T | 4 | a0001c0001t0001g0178a0001c0007t0004g0044a0001c0007t0004g0046others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+683C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517344 | ||||||
| chr3:12517357
|
C | CAAAAAAA others(4): Show |
1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.960+700_960+710dup others(11): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517357 | |||||
| chr3:12517357
|
C | CAAAAAAA others(5): Show |
10 | a0001c0001t0002g0057a0001c0001t0002g0084a0001c0001t0002g0085others(7): Show | 10 | HG00140.hp2 HG02615.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.960+699_960+710dup others(12): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517357 | |||||
| chr3:12517357
|
C | CAAAAAAA others(6): Show |
99 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(96): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.960+698_960+710dup others(13): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517357 | |||||
| chr3:12517357
|
C | CAAAAAAA others(7): Show |
36 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0078others(33): Show | 38 | HG00423.hp1 HG00733.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.960+697_960+710dup others(14): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517357 | |||||
| chr3:12517357
|
C | CAAAAAAA others(8): Show |
3 | a0002c0003t0002g0024a0002c0003t0002g0026a0002c0006t0005g0238 | 3 | HG02055.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.960+710_960+711ins others(15): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517357 | |||||
| chr3:12517357
|
C | CAAAAAAA others(9): Show |
9 | a0002c0004t0001g0147a0002c0004t0001g0149a0002c0004t0001g0150others(6): Show | 10 | HG01243.hp2 HG01934.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.960+710_960+711ins others(16): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517357 | |||||
| chr3:12517357
|
C | CAAAAAAA others(10): Show |
5 | a0002c0004t0007g0032a0002c0004t0007g0037a0002c0004t0007g0038others(2): Show | 5 | HG01928.hp2 HG01978.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+710_960+711ins others(17): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517357 | |||||
| chr3:12517357
|
C | CAAAAAAA others(11): Show |
1 | a0002c0004t0001g0148 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.960+710_960+711ins others(18): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517357 | |||||
| chr3:12517360
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0095 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.960+710_960+711ins others(13): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517360 | |||||
| chr3:12517391
|
C | A | 109 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.960+730C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517391 | ||||||
| chr3:12517666
|
G | A | 1 | a0002c0004t0001g0147 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.960+1005G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517666 | ||||||
| chr3:12517689
|
G | A | 25 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0059others(22): Show | 27 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.960+1028G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517689 | ||||||
| chr3:12517764
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.960+1103G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517764 | ||||||
| chr3:12517818
|
A | G | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.960+1157A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517818 | ||||||
| chr3:12517887
|
T | G | 166 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.961-1172T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517887 | ||||||
| chr3:12517912
|
T | C | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-1147T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517912 | ||||||
| chr3:12517917
|
T | C | 4 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(1): Show | 4 | NA18948.hp1 NA18951.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-1142T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517917 | ||||||
| chr3:12517938
|
C | CA | 20 | a0001c0001t0001g0167a0001c0010t0001g0151a0002c0003t0002g0030others(17): Show | 21 | HG01243.hp2 HG01928.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.961-1111dupA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12517938 | |||||
| chr3:12517948
|
A | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG02040.hp1 NA18966.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.961-1111A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12517948 | ||||||
| chr3:12518429
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-630G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518429 | ||||||
| chr3:12518445
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-614C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518445 | ||||||
| chr3:12518450
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-609C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518450 | ||||||
| chr3:12518452
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-607A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518452 | ||||||
| chr3:12518464
|
T | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-595T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518464 | ||||||
| chr3:12518468
|
G | C | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-591G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518468 | ||||||
| chr3:12518469
|
T | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-590T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518469 | ||||||
| chr3:12518474
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-585T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518474 | ||||||
| chr3:12518476
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-583C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518476 | ||||||
| chr3:12518478
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-581C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518478 | ||||||
| chr3:12518479
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-580T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518479 | ||||||
| chr3:12518481
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-578A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518481 | ||||||
| chr3:12518483
|
T | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-576T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518483 | ||||||
| chr3:12518485
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-574C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518485 | ||||||
| chr3:12518499
|
A | C | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-560A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518499 | ||||||
| chr3:12518504
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-555G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518504 | ||||||
| chr3:12518506
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-553C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518506 | ||||||
| chr3:12518515
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-544G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518515 | ||||||
| chr3:12518521
|
T | A | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-538T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518521 | ||||||
| chr3:12518523
|
G | C | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-536G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518523 | ||||||
| chr3:12518537
|
A | ATTAGCAG others(18): Show |
1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-522_961-521ins others(25): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518537 | ||||||
| chr3:12518538
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-521A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518538 | ||||||
| chr3:12518572
|
T | C | 20 | a0001c0001t0013g0214a0003c0002t0003g0006a0003c0002t0003g0022others(17): Show | 24 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.961-487T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518572 | ||||||
| chr3:12518683
|
T | C | 11 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0065others(8): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.961-376T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518683 | ||||||
| chr3:12518704
|
CT | C | 129 | a0001c0001t0001g0202a0001c0001t0002g0002a0001c0001t0002g0011others(126): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.961-341delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 12518704 | |||||
| chr3:12518818
|
A | G | 166 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.961-241A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518818 | ||||||
| chr3:12518965
|
A | G | 1 | a0001c0001t0011g0185 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.961-94A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12518965 | ||||||
| chr3:12519005
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.961-54G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12519005 | ||||||
| chr3:12519034
|
T | A | 1 | a0001c0001t0006g0115 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.961-25T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 7/11 | chr3 | 12519034 | ||||||
| chr3:12519264
|
A | T | 109 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1099+67A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519264 | ||||||
| chr3:12519382
|
G | C | 1 | a0001c0001t0002g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099+185G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519382 | ||||||
| chr3:12519417
|
T | G | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099+220T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519417 | ||||||
| chr3:12519463
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1099+266T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519463 | ||||||
| chr3:12519526
|
A | C | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+329A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519526 | ||||||
| chr3:12519569
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1099+372C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519569 | ||||||
| chr3:12519575
|
C | A | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099+378C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519575 | ||||||
| chr3:12519588
|
T | C | 4 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(1): Show | 9 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099+391T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519588 | ||||||
| chr3:12519612
|
A | G | 139 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(136): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1099+415A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519612 | ||||||
| chr3:12519639
|
G | A | 8 | a0001c0001t0004g0052a0001c0001t0004g0053a0001c0001t0004g0056others(5): Show | 8 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099+442G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519639 | ||||||
| chr3:12519670
|
C | T | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+473C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519670 | ||||||
| chr3:12519671
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1099+474G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519671 | ||||||
| chr3:12519740
|
G | A | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099+543G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519740 | ||||||
| chr3:12519749
|
G | GA | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+552_1099+553i others(3): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519749 | ||||||
| chr3:12519750
|
G | A | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1099+553G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519750 | ||||||
| chr3:12519836
|
G | A | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099+639G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519836 | ||||||
| chr3:12519933
|
C | G | 1 | a0004c0009t0009g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1099+736C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519933 | ||||||
| chr3:12519970
|
C | T | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099+773C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12519970 | ||||||
| chr3:12520002
|
C | CT | 29 | a0001c0010t0001g0151a0002c0003t0002g0008a0002c0003t0002g0009others(26): Show | 32 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1099+818dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12520002 | |||||
| chr3:12520028
|
C | T | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+831C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520028 | ||||||
| chr3:12520053
|
C | T | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+856C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520053 | ||||||
| chr3:12520067
|
T | C | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+870T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520067 | ||||||
| chr3:12520088
|
C | T | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099+891C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520088 | ||||||
| chr3:12520103
|
G | A | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+906G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520103 | ||||||
| chr3:12520123
|
C | T | 113 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1099+926C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520123 | ||||||
| chr3:12520163
|
T | C | 1 | a0001c0001t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1099+966T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520163 | ||||||
| chr3:12520177
|
G | T | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099+980G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520177 | ||||||
| chr3:12520199
|
C | A | 1 | a0001c0001t0002g0106 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1099+1002C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520199 | ||||||
| chr3:12520199
|
C | T | 21 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(18): Show | 24 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1099+1002C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520199 | ||||||
| chr3:12520349
|
T | G | 16 | a0001c0010t0001g0151a0002c0004t0001g0147a0002c0004t0001g0148others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099+1152T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520349 | ||||||
| chr3:12520411
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1099+1214C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520411 | ||||||
| chr3:12520714
|
C | T | 1 | a0001c0001t0004g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1099+1517C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520714 | ||||||
| chr3:12520771
|
C | CAGAG | 142 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(139): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1099+1576_1099+157 others(8): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12520771 | |||||
| chr3:12520798
|
T | A | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099+1601T>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520798 | ||||||
| chr3:12520804
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1099+1607G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520804 | ||||||
| chr3:12520816
|
C | T | 1 | a0001c0007t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1099+1619C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520816 | ||||||
| chr3:12520914
|
C | T | 126 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(123): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1099+1717C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520914 | ||||||
| chr3:12520950
|
T | C | 13 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(10): Show | 15 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099+1753T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12520950 | ||||||
| chr3:12521027
|
G | A | 7 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(4): Show | 7 | HG02135.hp1 HG03491.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099+1830G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521027 | ||||||
| chr3:12521138
|
C | A | 140 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(137): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1099+1941C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521138 | ||||||
| chr3:12521150
|
T | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0065others(37): Show | 50 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1099+1953T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521150 | ||||||
| chr3:12521161
|
A | G | 4 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(1): Show | 9 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099+1964A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521161 | ||||||
| chr3:12521531
|
G | A | 10 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(7): Show | 12 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1099+2334G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521531 | ||||||
| chr3:12521662
|
C | A | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1099+2465C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521662 | ||||||
| chr3:12521666
|
G | A | 113 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1099+2469G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521666 | ||||||
| chr3:12521739
|
C | T | 2 | a0001c0007t0004g0044a0001c0007t0004g0046 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1099+2542C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521739 | ||||||
| chr3:12521750
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0004g0054 | 2 | HG03453.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1099+2553G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521750 | ||||||
| chr3:12521880
|
A | G | 141 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(138): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1099+2683A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521880 | ||||||
| chr3:12521966
|
G | A | 109 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1099+2769G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12521966 | ||||||
| chr3:12522006
|
CAAAAAAT others(6): Show |
C | 1 | a0001c0001t0002g0130 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1099+2819_1099+283 others(17): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12522006 | |||||
| chr3:12522016
|
TAATAAAA others(6): Show |
T | 108 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(105): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1099+2836_1099+284 others(17): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12522016 | |||||
| chr3:12522140
|
T | C | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1099+2943T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12522140 | ||||||
| chr3:12522141
|
T | C | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1099+2944T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12522141 | ||||||
| chr3:12522187
|
G | A | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+2990G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12522187 | ||||||
| chr3:12522303
|
C | G | 1 | a0001c0001t0002g0106 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1099+3106C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12522303 | ||||||
| chr3:12522363
|
A | ATGTACAA others(13): Show |
2 | a0001c0001t0002g0070a0001c0007t0004g0047 | 2 | HG02280.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1099+3179_1099+319 others(24): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12522363 | |||||
| chr3:12522421
|
A | AC | 13 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(10): Show | 15 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099+3225dupC | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12522421 | |||||
| chr3:12522534
|
A | G | 93 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(90): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1099+3337A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12522534 | ||||||
| chr3:12522583
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1099+3386T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12522583 | ||||||
| chr3:12522803
|
A | G | 113 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1099+3606A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12522803 | ||||||
| chr3:12522843
|
A | G | 2 | a0002c0003t0002g0024a0002c0003t0002g0029 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1099+3646A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12522843 | ||||||
| chr3:12523037
|
T | G | 25 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(22): Show | 28 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1099+3840T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12523037 | ||||||
| chr3:12523290
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1099+4093A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12523290 | ||||||
| chr3:12523446
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19007.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1099+4249G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12523446 | ||||||
| chr3:12523526
|
C | CT | 11 | a0001c0001t0001g0019a0001c0001t0001g0157a0001c0001t0001g0160others(8): Show | 12 | HG00423.hp1 HG00423.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1099+4354dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTT | 24 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(21): Show | 27 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1099+4353_1099+435 others(6): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0004g0053 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1099+4345_1099+435 others(14): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0004g0052a0001c0001t0004g0069a0001c0001t0005g0096 | 3 | HG01123.hp2 HG01516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1099+4344_1099+435 others(15): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0004g0068a0001c0001t0010g0154 | 2 | HG01358.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1099+4343_1099+435 others(16): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0004g0110a0001c0001t0006g0117 | 2 | HG01261.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1099+4342_1099+435 others(17): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0002g0107a0001c0001t0002g0135a0001c0001t0006g0118others(2): Show | 5 | HG06807.hp1 NA18946.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+4340_1099+435 others(19): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(9): Show |
17 | a0001c0001t0002g0050a0001c0001t0002g0055a0001c0001t0002g0082others(14): Show | 17 | HG00733.hp1 HG01192.hp2 HG02896.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099+4339_1099+435 others(20): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(10): Show |
15 | a0001c0001t0002g0013a0001c0001t0002g0057a0001c0001t0002g0060others(12): Show | 16 | HG00099.hp2 HG01074.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1099+4338_1099+435 others(21): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(11): Show |
18 | a0001c0001t0002g0011a0001c0001t0002g0021a0001c0001t0002g0051others(15): Show | 20 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1099+4337_1099+435 others(22): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(12): Show |
12 | a0001c0001t0002g0012a0001c0001t0002g0014a0001c0001t0002g0058others(9): Show | 14 | HG00280.hp1 HG00639.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1099+4336_1099+435 others(23): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(13): Show |
3 | a0001c0001t0002g0059a0001c0001t0002g0098a0001c0001t0018g0061 | 3 | HG02559.hp1 HG02886.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1099+4335_1099+435 others(24): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0002g0136a0001c0007t0004g0047 | 2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1099+4334_1099+435 others(25): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0002g0097a0001c0007t0004g0044 | 2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1099+4333_1099+435 others(26): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002g0095 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1099+4332_1099+435 others(27): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(18): Show |
3 | a0001c0001t0001g0182a0001c0001t0004g0054a0001c0001t0005g0083 | 3 | HG03453.hp1 HG03453.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1099+4330_1099+435 others(29): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0002g0063a0001c0001t0002g0080a0001c0001t0002g0092 | 3 | NA18977.hp1 NA18998.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1099+4354_1099+435 others(30): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0002g0062 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099+4354_1099+435 others(31): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
CTTTT | C | 15 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0048others(12): Show | 22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1099+4351_1099+435 others(8): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523526
|
CTTTTT | C | 6 | a0002c0003t0004g0016a0002c0003t0004g0138a0002c0003t0004g0139others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099+4350_1099+435 others(9): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12523526 | |||||
| chr3:12523619
|
A | G | 1 | a0003c0002t0003g0215 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1099+4422A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12523619 | ||||||
| chr3:12523729
|
A | G | 142 | a0001c0001t0001g0182a0001c0001t0002g0002a0001c0001t0002g0011others(139): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1099+4532A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12523729 | ||||||
| chr3:12523775
|
A | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1099+4578A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12523775 | ||||||
| chr3:12523836
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1099+4639G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12523836 | ||||||
| chr3:12524209
|
G | A | 3 | a0001c0007t0004g0044a0001c0007t0004g0046a0001c0007t0004g0047 | 3 | HG02145.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1100-4679G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524209 | ||||||
| chr3:12524297
|
T | C | 142 | a0001c0001t0001g0182a0001c0001t0002g0002a0001c0001t0002g0011others(139): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1100-4591T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524297 | ||||||
| chr3:12524320
|
G | A | 4 | a0001c0001t0004g0045a0001c0001t0005g0043a0001c0001t0005g0083others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-4568G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524320 | ||||||
| chr3:12524323
|
G | T | 3 | a0001c0007t0004g0044a0001c0007t0004g0046a0001c0007t0004g0047 | 3 | HG02145.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1100-4565G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524323 | ||||||
| chr3:12524405
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0183a0001c0001t0001g0189others(4): Show | 8 | HG00140.hp1 HG01070.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1100-4483C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524405 | ||||||
| chr3:12524561
|
G | A | 1 | a0002c0004t0009g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1100-4327G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524561 | ||||||
| chr3:12524587
|
C | G | 1 | a0001c0001t0006g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1100-4301C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524587 | ||||||
| chr3:12524649
|
C | T | 3 | a0001c0001t0002g0060a0001c0008t0002g0086a0001c0008t0002g0087 | 3 | HG02809.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1100-4239C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524649 | ||||||
| chr3:12524685
|
A | T | 1 | a0001c0001t0004g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1100-4203A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524685 | ||||||
| chr3:12524739
|
C | CTT | 106 | a0001c0001t0001g0182a0001c0001t0002g0002a0001c0001t0002g0011others(103): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1100-4132_1100-413 others(6): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12524739 | |||||
| chr3:12524739
|
C | CTTT | 16 | a0001c0001t0002g0058a0001c0010t0001g0151a0002c0004t0001g0147others(13): Show | 17 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1100-4133_1100-413 others(7): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12524739 | |||||
| chr3:12524740
|
T | TC | 3 | a0001c0007t0004g0044a0001c0007t0004g0046a0001c0007t0004g0047 | 3 | HG02145.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1100-4148_1100-414 others(5): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524740 | ||||||
| chr3:12524741
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1100-4147T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524741 | ||||||
| chr3:12524956
|
C | T | 5 | a0002c0004t0007g0010a0002c0004t0007g0035a0002c0004t0007g0037others(2): Show | 6 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100-3932C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12524956 | ||||||
| chr3:12525069
|
A | G | 24 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(21): Show | 33 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1100-3819A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525069 | ||||||
| chr3:12525136
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1100-3752A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525136 | ||||||
| chr3:12525189
|
C | T | 1 | a0001c0001t0002g0021 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1100-3699C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525189 | ||||||
| chr3:12525544
|
A | AT | 52 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(49): Show | 64 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1100-3339dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12525544 | |||||
| chr3:12525668
|
C | T | 2 | a0001c0001t0006g0122a0001c0001t0006g0126 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1100-3220C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525668 | ||||||
| chr3:12525696
|
A | G | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1100-3192A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525696 | ||||||
| chr3:12525739
|
G | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3149G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525739 | ||||||
| chr3:12525740
|
A | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3148A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525740 | ||||||
| chr3:12525747
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3141T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525747 | ||||||
| chr3:12525753
|
A | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3135A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525753 | ||||||
| chr3:12525754
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3134A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525754 | ||||||
| chr3:12525763
|
A | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3125A>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525763 | ||||||
| chr3:12525764
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3124T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525764 | ||||||
| chr3:12525765
|
G | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3123G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525765 | ||||||
| chr3:12525780
|
G | A | 1 | a0001c0011t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1100-3108G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525780 | ||||||
| chr3:12525801
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(235): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1100-3087A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525801 | ||||||
| chr3:12525855
|
G | A | 5 | a0001c0001t0001g0199a0001c0005t0003g0004a0001c0005t0003g0023others(2): Show | 10 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1100-3033G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525855 | ||||||
| chr3:12525953
|
A | G | 4 | a0001c0001t0001g0146a0001c0001t0001g0197a0001c0001t0011g0184others(1): Show | 4 | HG00673.hp1 HG01256.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-2935A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12525953 | ||||||
| chr3:12526144
|
G | A | 4 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(1): Show | 9 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1100-2744G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526144 | ||||||
| chr3:12526165
|
C | G | 1 | a0003c0002t0003g0022 | 2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1100-2723C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526165 | ||||||
| chr3:12526178
|
C | A | 115 | a0001c0001t0001g0166a0001c0001t0002g0002a0001c0001t0002g0011others(112): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1100-2710C>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526178 | ||||||
| chr3:12526182
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1100-2706A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526182 | ||||||
| chr3:12526358
|
A | G | 13 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(10): Show | 15 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1100-2530A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526358 | ||||||
| chr3:12526419
|
A | G | 4 | a0001c0001t0002g0055a0001c0001t0002g0106a0001c0001t0002g0107others(1): Show | 4 | NA18969.hp1 NA18971.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-2469A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526419 | ||||||
| chr3:12526778
|
G | C | 1 | a0002c0006t0005g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1100-2110G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526778 | ||||||
| chr3:12526843
|
C | T | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1100-2045C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526843 | ||||||
| chr3:12526863
|
T | G | 13 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(10): Show | 15 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1100-2025T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526863 | ||||||
| chr3:12526926
|
T | G | 141 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(138): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1100-1962T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12526926 | ||||||
| chr3:12527054
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1100-1834G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527054 | ||||||
| chr3:12527082
|
T | G | 16 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0048others(13): Show | 23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1100-1806T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527082 | ||||||
| chr3:12527178
|
C | G | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1100-1710C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527178 | ||||||
| chr3:12527456
|
C | CT | 6 | a0001c0001t0001g0177a0001c0001t0001g0197a0001c0001t0005g0131others(3): Show | 7 | HG01081.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1100-1417dupT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12527456 | |||||
| chr3:12527456
|
C | CTTT | 13 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(10): Show | 14 | HG01243.hp2 HG01928.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.1100-1419_1100-141 others(7): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 12527456 | |||||
| chr3:12527456
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1100-1432C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527456 | ||||||
| chr3:12527457
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0181 | 2 | HG03491.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1100-1431T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527457 | ||||||
| chr3:12527487
|
T | C | 1 | a0001c0005t0003g0023 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1100-1401T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527487 | ||||||
| chr3:12527515
|
G | A | 1 | a0001c0007t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1100-1373G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527515 | ||||||
| chr3:12527536
|
C | T | 24 | a0001c0005t0003g0004a0001c0005t0003g0023a0001c0005t0003g0232others(21): Show | 33 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1100-1352C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527536 | ||||||
| chr3:12527741
|
C | T | 1 | a0001c0001t0005g0114 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1100-1147C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527741 | ||||||
| chr3:12527901
|
C | G | 1 | a0001c0001t0002g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1100-987C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527901 | ||||||
| chr3:12527956
|
G | A | 3 | a0003c0002t0003g0220a0003c0002t0003g0224a0003c0002t0003g0225 | 3 | HG02630.hp2 HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1100-932G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12527956 | ||||||
| chr3:12528027
|
C | G | 1 | a0001c0010t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1100-861C>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528027 | ||||||
| chr3:12528186
|
A | G | 1 | a0001c0001t0006g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1100-702A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528186 | ||||||
| chr3:12528198
|
G | A | 2 | a0001c0001t0002g0064a0001c0001t0002g0079 | 2 | HG01175.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1100-690G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528198 | ||||||
| chr3:12528305
|
G | C | 3 | a0001c0001t0004g0045a0001c0007t0004g0044a0001c0007t0004g0046 | 3 | HG02145.hp1 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1100-583G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528305 | ||||||
| chr3:12528461
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0127 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1100-427C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528461 | ||||||
| chr3:12528469
|
C | T | 13 | a0002c0003t0002g0008a0002c0003t0002g0009a0002c0003t0002g0024others(10): Show | 15 | HG01074.hp2 HG01099.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1100-419C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528469 | ||||||
| chr3:12528525
|
G | A | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1100-363G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528525 | ||||||
| chr3:12528551
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(232): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1100-337T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528551 | ||||||
| chr3:12528628
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1100-260G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 8/11 | chr3 | 12528628 | ||||||
| chr3:12529072
|
A | G | 1 | a0001c0001t0013g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1136+148A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529072 | ||||||
| chr3:12529073
|
C | T | 108 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(105): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1136+149C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529073 | ||||||
| chr3:12529194
|
C | T | 1 | a0002c0003t0002g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1136+270C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529194 | ||||||
| chr3:12529387
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1137-375A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529387 | ||||||
| chr3:12529391
|
A | G | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1137-371A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529391 | ||||||
| chr3:12529444
|
T | C | 1 | a0001c0001t0015g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1137-318T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529444 | ||||||
| chr3:12529450
|
A | T | 1 | a0001c0011t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1137-312A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529450 | ||||||
| chr3:12529465
|
C | CA | 104 | a0001c0001t0001g0156a0001c0001t0001g0174a0001c0001t0001g0178others(101): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1137-277dupA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 12529465 | |||||
| chr3:12529465
|
C | CAA | 8 | a0001c0001t0002g0048a0001c0001t0002g0062a0001c0001t0002g0078others(5): Show | 8 | HG01346.hp1 HG01361.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-278_1137-277d others(4): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 12529465 | |||||
| chr3:12529465
|
CA | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0005t0003g0004others(4): Show | 12 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137-277delA | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 12529465 | |||||
| chr3:12529487
|
T | C | 165 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1137-275T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529487 | ||||||
| chr3:12529656
|
G | A | 1 | a0001c0012t0017g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1137-106G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 9/11 | chr3 | 12529656 | ||||||
| chr3:12529884
|
A | T | 1 | a0002c0003t0002g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1248+11A>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | chr3 | 12529884 | ||||||
| chr3:12529921
|
GT | G | 24 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(21): Show | 27 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1248+61delT | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 12529921 | |||||
| chr3:12530039
|
G | A | 1 | a0001c0011t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1248+166G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | chr3 | 12530039 | ||||||
| chr3:12530225
|
CAT | C | 15 | a0002c0004t0001g0147a0002c0004t0001g0148a0002c0004t0001g0149others(12): Show | 16 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1248+355_1248+356d others(4): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 12530225 | |||||
| chr3:12530257
|
T | C | 2 | a0001c0001t0002g0130a0001c0007t0004g0047 | 2 | HG02280.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1248+384T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | chr3 | 12530257 | ||||||
| chr3:12530358
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1248+485C>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | chr3 | 12530358 | ||||||
| chr3:12530685
|
G | T | 7 | a0001c0001t0004g0052a0001c0001t0004g0053a0001c0001t0004g0068others(4): Show | 7 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1248+812G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | chr3 | 12530685 | ||||||
| chr3:12530721
|
G | C | 2 | a0001c0001t0002g0130a0001c0007t0004g0047 | 2 | HG02280.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1248+848G>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | chr3 | 12530721 | ||||||
| chr3:12530857
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1249-713A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | chr3 | 12530857 | ||||||
| chr3:12530913
|
T | G | 1 | a0001c0001t0002g0012 | 2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1249-657T>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | chr3 | 12530913 | ||||||
| chr3:12531205
|
A | ACAATT | 138 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(135): Show | 154 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.1249-362_1249-361i others(7): Show |
TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 12531205 | |||||
| chr3:12531837
|
A | G | 92 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(89): Show | 99 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.1338+178A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12531837 | ||||||
| chr3:12531841
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1338+182T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12531841 | ||||||
| chr3:12531871
|
T | C | 1 | a0001c0001t0001g0018 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1338+212T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12531871 | ||||||
| chr3:12532019
|
A | G | 90 | a0001c0001t0001g0157a0001c0001t0001g0170a0001c0001t0002g0002others(87): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1338+360A>G | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12532019 | ||||||
| chr3:12532258
|
T | C | 1 | a0001c0001t0013g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1339-404T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12532258 | ||||||
| chr3:12532323
|
G | A | 3 | a0003c0002t0003g0229a0003c0002t0003g0230a0003c0002t0003g0231 | 3 | HG00099.hp1 HG01993.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1339-339G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12532323 | ||||||
| chr3:12532375
|
T | C | 1 | a0001c0001t0004g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1339-287T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12532375 | ||||||
| chr3:12532391
|
G | A | 1 | a0001c0001t0006g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1339-271G>A | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12532391 | ||||||
| chr3:12532499
|
T | C | 99 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(96): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1339-163T>C | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12532499 | ||||||
| chr3:12532638
|
G | T | 7 | a0002c0004t0007g0010a0002c0004t0007g0032a0002c0004t0007g0033others(4): Show | 8 | HG01243.hp2 HG01928.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339-24G>T | TSEN2 | ENSG00000154743.19 | transcript | ENST00000284995.11 | protein_coding | 11/11 | chr3 | 12532638 |