Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 113878 |
|---|---|
| ensemblid | ENSG00000091073.20 |
| hgncid | 15973 |
| symbol | DTX2 |
| name | deltex E3 ubiquitin ligase 2 |
| refseq_nuc | NM_001102594.3 |
| refseq_prot | NP_001096064.1 |
| ensembl_nuc | ENST00000430490.7 |
| ensembl_prot | ENSP00000411986.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 76461709 |
| end | 76505991 |
| strand | + |
| ver | v1.2 |
| region | chr7:76461709-76505991 |
| region5000 | chr7:76456709-76510991 |
| regionname0 | DTX2_chr7_76461709_76505991 |
| regionname5000 | DTX2_chr7_76456709_76510991 |
| 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 | 0/0 | 622 | 146 | 40 | 24 | 60 | 5 | 17 | 36 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002 | 0/0 | 622 | 65 | 12 | 20 | 24 | 2 | 7 | 10 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0003 | 0/1 | 622 | 38 | 14 | 13 | 1 | 2 | 7 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0004 | 0/0 | 622 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005 | 0/0 | 352 | 9 | 2 | 2 | 4 | 0 | 1 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0006 | 0/0 | 622 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0007 | 0/0 | 622 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0008 | 0/0 | 352 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0009 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0010 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0011 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0012 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0013 | 1/0 | 622 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0014 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1869 | 111 | 18 | 19 | 54 | 4 | 16 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0002 | 0/0 | 1869 | 44 | 3 | 17 | 16 | 2 | 6 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0003 | 0/0 | 1869 | 31 | 20 | 4 | 5 | 1 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0004 | 0/1 | 1869 | 25 | 5 | 11 | 1 | 2 | 5 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0005 | 0/0 | 1869 | 13 | 9 | 2 | 0 | 0 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0006 | 0/0 | 1869 | 9 | 8 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0007 | 0/0 | 1869 | 9 | 0 | 2 | 7 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0008 | 0/0 | 1869 | 5 | 5 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0009 | 0/0 | 1870 | 5 | 0 | 1 | 3 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0010 | 0/0 | 1869 | 3 | 0 | 0 | 0 | 1 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0011 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0012 | 0/0 | 1869 | 2 | 1 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0013 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0014 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0015 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0016 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0017 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0018 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0019 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0020 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0021 | 1/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0022 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0023 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0024 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0025 | 0/0 | 1870 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0026 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0027 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0028 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0029 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0030 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0031 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0032 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| c0033 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| 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 | 773 | 149 | 54 | 40 | 33 | 4 | 16 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0002 | 0/0 | 773 | 117 | 18 | 19 | 57 | 5 | 18 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0003 | 0/0 | 773 | 3 | 3 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0004 | 0/0 | 773 | 3 | 3 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0005 | 0/0 | 773 | 2 | 0 | 1 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0006 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0007 | 0/0 | 773 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0008 | 0/0 | 773 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0009 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0010 | 0/0 | 773 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| t0011 | 0/0 | 773 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1869 | 111 | 18 | 19 | 54 | 4 | 16 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0003 | 0/0 | 1869 | 31 | 20 | 4 | 5 | 1 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0013 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0018 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0023 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0031 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0002 | 0/0 | 1869 | 44 | 3 | 17 | 16 | 2 | 6 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0007 | 0/0 | 1869 | 9 | 0 | 2 | 7 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0008 | 0/0 | 1869 | 5 | 5 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0011 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0017 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0020 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0028 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0029 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0032 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0003c0004 | 0/1 | 1869 | 25 | 5 | 11 | 1 | 2 | 5 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0003c0005 | 0/0 | 1869 | 13 | 9 | 2 | 0 | 0 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0004c0006 | 0/0 | 1869 | 9 | 8 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0004c0024 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0009 | 0/0 | 1870 | 5 | 0 | 1 | 3 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0025 | 0/0 | 1870 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0026 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0027 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0033 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0006c0010 | 0/0 | 1869 | 3 | 0 | 0 | 0 | 1 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0007c0012 | 0/0 | 1869 | 2 | 1 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0008c0014 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0009c0015 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0010c0030 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0011c0019 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0012c0022 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0013c0021 | 1/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0014c0016 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0001t0002 | 0/0 | 2641 | 109 | 18 | 18 | 54 | 4 | 15 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0001t0010 | 0/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0003t0001 | 0/0 | 2641 | 31 | 20 | 4 | 5 | 1 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0013t0001 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0018t0011 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0023t0006 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0001c0031t0001 | 0/0 | 2641 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0002t0001 | 0/0 | 2641 | 41 | 3 | 15 | 16 | 1 | 6 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0002t0005 | 0/0 | 2641 | 2 | 0 | 1 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0002t0007 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0007t0001 | 0/0 | 2641 | 9 | 0 | 2 | 7 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0008t0001 | 0/0 | 2641 | 2 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0008t0004 | 0/0 | 2641 | 3 | 3 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0011t0003 | 0/0 | 2641 | 2 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0017t0001 | 0/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0020t0009 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0028t0001 | 0/0 | 2641 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0029t0001 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0002c0032t0001 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0003c0004t0001 | 0/1 | 2641 | 25 | 5 | 11 | 1 | 2 | 5 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0003c0005t0001 | 0/0 | 2641 | 13 | 9 | 2 | 0 | 0 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0004c0006t0001 | 0/0 | 2641 | 9 | 8 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0004c0024t0001 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0009t0002 | 0/0 | 2642 | 4 | 0 | 1 | 3 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0009t0008 | 0/0 | 2642 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0025t0001 | 0/0 | 2642 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0026t0001 | 0/0 | 2642 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0027t0001 | 0/0 | 2642 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0005c0033t0001 | 0/0 | 2642 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0006c0010t0002 | 0/0 | 2641 | 3 | 0 | 0 | 0 | 1 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0007c0012t0001 | 0/0 | 2641 | 2 | 1 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0008c0014t0001 | 0/0 | 2642 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0009c0015t0001 | 0/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0010c0030t0003 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0011c0019t0001 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0012c0022t0002 | 0/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0013c0021t0001 | 1/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| a0014c0016t0001 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | copy fasta | chr7 | 76456709 | 76510991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0013t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0018t0011g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0023t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0001c0031t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0002t0007g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0007t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0008t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0008t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0008t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0008t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0008t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0011t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0011t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0017t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0020t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0028t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0029t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0002c0032t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0003c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0006t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0004c0024t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0009t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0009t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0009t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0009t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0009t0008g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0025t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0026t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0027t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0005c0033t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0006c0010t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0006c0010t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0006c0010t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0007c0012t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0007c0012t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0008c0014t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0009c0015t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0010c0030t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0011c0019t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0012c0022t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0013c0021t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| a0014c0016t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00140 | hp2 | a0003 | c0004 | t0001 | g0240 | EUR | GBR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0204 | EUR | FIN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0135 | EUR | FIN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0148 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00544 | hp1 | a0001 | c0031 | t0001 | g0273 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00558 | hp2 | a0002 | c0007 | t0001 | g0271 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00609 | hp2 | a0002 | c0007 | t0001 | g0276 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00621 | hp2 | a0005 | c0009 | t0002 | g0172 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00639 | hp1 | a0007 | c0012 | t0001 | g0245 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00639 | hp2 | a0003 | c0005 | t0001 | g0016 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00733 | hp1 | a0002 | c0032 | t0001 | g0256 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00735 | hp1 | a0003 | c0004 | t0001 | g0250 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00735 | hp2 | a0002 | c0002 | t0005 | g0006 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01081 | hp1 | a0003 | c0004 | t0001 | g0241 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01099 | hp1 | a0003 | c0004 | t0001 | g0243 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01109 | hp1 | a0004 | c0006 | t0001 | g0124 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0254 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0236 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01168 | hp2 | a0003 | c0004 | t0001 | g0242 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01175 | hp1 | a0003 | c0004 | t0001 | g0251 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0158 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01192 | hp1 | a0003 | c0005 | t0001 | g0015 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01243 | hp1 | a0004 | c0024 | t0001 | g0159 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01243 | hp2 | a0005 | c0025 | t0001 | g0143 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01261 | hp1 | a0003 | c0004 | t0001 | g0255 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01346 | hp1 | a0001 | c0018 | t0011 | g0094 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01358 | hp2 | a0003 | c0004 | t0001 | g0253 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01496 | hp2 | a0002 | c0007 | t0001 | g0259 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01884 | hp1 | a0004 | c0006 | t0001 | g0121 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01884 | hp2 | a0002 | c0008 | t0004 | g0134 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0154 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0128 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0213 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0131 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01993 | hp2 | a0003 | c0004 | t0001 | g0244 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02055 | hp1 | a0005 | c0033 | t0001 | g0233 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02055 | hp2 | a0011 | c0019 | t0001 | g0027 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02056 | hp2 | a0002 | c0028 | t0001 | g0258 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02080 | hp2 | a0005 | c0009 | t0002 | g0164 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02083 | hp1 | a0002 | c0007 | t0001 | g0185 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02129 | hp1 | a0002 | c0007 | t0001 | g0272 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02135 | hp2 | a0003 | c0004 | t0001 | g0257 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02148 | hp1 | a0005 | c0009 | t0002 | g0101 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0202 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CDX | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CDX | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02258 | hp1 | a0003 | c0004 | t0001 | g0248 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02258 | hp2 | a0004 | c0006 | t0001 | g0120 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0130 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02293 | hp1 | a0002 | c0007 | t0001 | g0260 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02293 | hp2 | a0002 | c0002 | t0007 | g0201 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02451 | hp2 | a0001 | c0023 | t0006 | g0023 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02523 | hp2 | a0005 | c0026 | t0001 | g0269 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02683 | hp2 | a0003 | c0005 | t0001 | g0026 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02698 | hp1 | a0001 | c0001 | t0010 | g0086 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0212 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02717 | hp1 | a0002 | c0008 | t0004 | g0133 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02818 | hp2 | a0003 | c0005 | t0001 | g0018 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02886 | hp2 | a0003 | c0005 | t0001 | g0022 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02896 | hp2 | a0003 | c0005 | t0001 | g0013 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02897 | hp1 | a0002 | c0020 | t0009 | g0011 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02897 | hp2 | a0003 | c0005 | t0001 | g0014 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02922 | hp2 | a0004 | c0006 | t0001 | g0117 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02965 | hp2 | a0004 | c0006 | t0001 | g0119 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03130 | hp1 | a0014 | c0016 | t0001 | g0227 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03139 | hp1 | a0003 | c0004 | t0001 | g0238 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0145 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03209 | hp2 | a0004 | c0006 | t0001 | g0118 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03225 | hp1 | a0002 | c0029 | t0001 | g0005 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0116 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03239 | hp2 | a0003 | c0005 | t0001 | g0025 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0138 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03486 | hp1 | a0002 | c0011 | t0003 | g0265 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0219 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03490 | hp1 | a0006 | c0010 | t0002 | g0010 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03490 | hp2 | a0003 | c0004 | t0001 | g0262 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03492 | hp2 | a0006 | c0010 | t0002 | g0098 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03516 | hp1 | a0003 | c0005 | t0001 | g0020 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03540 | hp2 | a0010 | c0030 | t0003 | g0263 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03579 | hp1 | a0007 | c0012 | t0001 | g0232 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03579 | hp2 | a0002 | c0008 | t0001 | g0229 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0211 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0192 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03704 | hp2 | a0003 | c0004 | t0001 | g0247 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03710 | hp2 | a0012 | c0022 | t0002 | g0091 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0225 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03927 | hp1 | a0003 | c0004 | t0001 | g0246 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03927 | hp2 | a0005 | c0009 | t0008 | g0073 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03942 | hp2 | a0009 | c0015 | t0001 | g0191 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0125 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0226 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04199 | hp1 | a0003 | c0004 | t0001 | g0252 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04199 | hp2 | a0002 | c0017 | t0001 | g0188 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0155 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18522 | hp1 | a0003 | c0005 | t0001 | g0024 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18522 | hp2 | a0004 | c0006 | t0001 | g0123 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | CHB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18906 | hp1 | a0003 | c0005 | t0001 | g0017 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18906 | hp2 | a0003 | c0004 | t0001 | g0239 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18947 | hp1 | a0002 | c0007 | t0001 | g0275 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18960 | hp2 | a0008 | c0014 | t0001 | g0210 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18983 | hp2 | a0002 | c0007 | t0001 | g0270 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19043 | hp1 | a0002 | c0011 | t0003 | g0264 | AFR | LWK | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | LWK | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19068 | hp1 | a0005 | c0009 | t0002 | g0162 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19074 | hp1 | a0002 | c0007 | t0001 | g0268 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19240 | hp1 | a0004 | c0006 | t0001 | g0115 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA19240 | hp2 | a0002 | c0008 | t0004 | g0132 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ASW | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20129 | hp2 | a0004 | c0006 | t0001 | g0122 | AFR | ASW | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20752 | hp1 | a0003 | c0004 | t0001 | g0237 | EUR | TSI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20752 | hp2 | a0002 | c0002 | t0005 | g0274 | EUR | TSI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20805 | hp1 | a0006 | c0010 | t0002 | g0087 | EUR | TSI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20905 | hp1 | a0003 | c0004 | t0001 | g0189 | SAS | GIH | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | GIH | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01123 | hp1 | a0003 | c0004 | t0001 | g0235 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02109 | hp1 | a0005 | c0027 | t0001 | g0139 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02109 | hp2 | a0002 | c0008 | t0001 | g0230 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02486 | hp1 | a0003 | c0004 | t0001 | g0249 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03471 | hp1 | a0001 | c0013 | t0001 | g0224 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG03471 | hp2 | a0003 | c0005 | t0001 | g0019 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG06807 | hp1 | a0003 | c0004 | t0001 | g0261 | AFR | USA | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| HG06807 | hp2 | a0003 | c0005 | t0001 | g0021 | AFR | USA | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | USA | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | USA | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0157 | AFR | LWK | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | LWK | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0004 | t0001 | g0234 | REF | REF | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| homoSapiens_grch38 | hp1 | a0013 | c0021 | t0001 | g0080 | REF | REF | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76482621
|
G | A | 1 | a0006 | 3 | HG03490.hp1 HG03492.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.382G>A | p.Val128Ile | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 764/2641 | 382/1869 | 128/622 | chr7 | 76482621 | ||
| chr7:76482880
|
A | AC | 2 | a0005a0008 | 10 | HG00621.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
frameshift_variant | HIGH | c.643dupC | p.Arg215fs | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1026/2641 | 644/1869 | 215/622 | INFO_REALIGN_3_PRIME | chr7 | 76482880 | |
| chr7:76483042
|
G | A | 1 | a0009 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.803G>A | p.Gly268Asp | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1185/2641 | 803/1869 | 268/622 | chr7 | 76483042 | ||
| chr7:76483129
|
C | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.890C>A | p.Ser297Tyr | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1272/2641 | 890/1869 | 297/622 | chr7 | 76483129 | ||
| chr7:76497420
|
C | T | 1 | a0004 | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
missense_variant | MODERATE | c.1093C>T | p.Arg365Cys | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/11 | 1475/2641 | 1093/1869 | 365/622 | chr7 | 76497420 | ||
| chr7:76497421
|
G | A | 1 | a0007 | 2 | HG00639.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.1094G>A | p.Arg365His | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/11 | 1476/2641 | 1094/1869 | 365/622 | chr7 | 76497421 | ||
| chr7:76500441
|
G | A | 10 | a0002a0003a0004others(7): Show | 123 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(120): Show |
missense_variant&splice_region_variant | MODERATE | c.1151G>A | p.Gly384Glu | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/11 | 1533/2641 | 1151/1869 | 384/622 | chr7 | 76500441 | ||
| chr7:76502328
|
A | G | 10 | a0001a0002a0004others(7): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
missense_variant | MODERATE | c.1261A>G | p.Thr421Ala | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1643/2641 | 1261/1869 | 421/622 | chr7 | 76502328 | ||
| chr7:76502332
|
C | T | 1 | a0011 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1265C>T | p.Ala422Val | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1647/2641 | 1265/1869 | 422/622 | chr7 | 76502332 | ||
| chr7:76502433
|
G | A | 1 | a0012 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1366G>A | p.Ala456Thr | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1748/2641 | 1366/1869 | 456/622 | chr7 | 76502433 | ||
| chr7:76505598
|
G | C | 1 | a0010 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1866G>C | p.Gln622His | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 2248/2641 | 1866/1869 | 622/622 | chr7 | 76505598 | ||
| chr7:76505989
|
A | G | 1 | a0002 | 1 | HG02897.hp1 | splice_region_variant | LOW | c.*388A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | chr7 | 76505989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76482518
|
G | A | 6 | a0001c0013a0002c0002a0002c0008others(3): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
synonymous_variant | LOW | c.279G>A | p.Arg93Arg | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 661/2641 | 279/1869 | 93/622 | chr7 | 76482518 | ||
| chr7:76482605
|
T | C | 1 | a0002c0017 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.366T>C | p.Thr122Thr | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 748/2641 | 366/1869 | 122/622 | chr7 | 76482605 | ||
| chr7:76482677
|
C | G | 3 | a0003c0004a0005c0033a0007c0012 | 28 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
synonymous_variant | LOW | c.438C>G | p.Ala146Ala | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 820/2641 | 438/1869 | 146/622 | chr7 | 76482677 | ||
| chr7:76482743
|
C | T | 23 | a0001c0003a0001c0013a0001c0031others(20): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
synonymous_variant | LOW | c.504C>T | p.Phe168Phe | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 886/2641 | 504/1869 | 168/622 | chr7 | 76482743 | ||
| chr7:76482782
|
G | A | 2 | a0001c0013a0001c0018 | 2 | HG01346.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.543G>A | p.Pro181Pro | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 925/2641 | 543/1869 | 181/622 | chr7 | 76482782 | ||
| chr7:76482806
|
G | A | 2 | a0004c0006a0004c0024 | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
synonymous_variant | LOW | c.567G>A | p.Pro189Pro | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 949/2641 | 567/1869 | 189/622 | chr7 | 76482806 | ||
| chr7:76482902
|
C | T | 1 | a0002c0032 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.663C>T | p.Leu221Leu | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1045/2641 | 663/1869 | 221/622 | chr7 | 76482902 | ||
| chr7:76482932
|
A | C | 1 | a0002c0032 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.693A>C | p.Pro231Pro | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1075/2641 | 693/1869 | 231/622 | chr7 | 76482932 | ||
| chr7:76483013
|
G | A | 1 | a0002c0028 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.774G>A | p.Ala258Ala | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1156/2641 | 774/1869 | 258/622 | chr7 | 76483013 | ||
| chr7:76492192
|
C | T | 5 | a0001c0013a0002c0002a0008c0014others(2): Show | 48 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(45): Show |
synonymous_variant | LOW | c.948C>T | p.Ser316Ser | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/11 | 1330/2641 | 948/1869 | 316/622 | chr7 | 76492192 | ||
| chr7:76502333
|
G | A | 5 | a0001c0001a0001c0018a0005c0009others(2): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
synonymous_variant | LOW | c.1266G>A | p.Ala422Ala | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1648/2641 | 1266/1869 | 422/622 | chr7 | 76502333 | ||
| chr7:76502378
|
A | G | 23 | a0001c0001a0001c0013a0001c0018others(20): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
synonymous_variant | LOW | c.1311A>G | p.Leu437Leu | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1693/2641 | 1311/1869 | 437/622 | chr7 | 76502378 | ||
| chr7:76503488
|
C | G | 3 | a0001c0023a0002c0011a0010c0030 | 4 | HG02451.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.1452C>G | p.Pro484Pro | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/11 | 1834/2641 | 1452/1869 | 484/622 | chr7 | 76503488 | ||
| chr7:76503551
|
C | T | 1 | a0004c0024 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1515C>T | p.Thr505Thr | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/11 | 1897/2641 | 1515/1869 | 505/622 | chr7 | 76503551 | ||
| chr7:76503581
|
T | C | 8 | a0001c0001a0001c0018a0001c0023others(5): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
synonymous_variant | LOW | c.1545T>C | p.Gly515Gly | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/11 | 1927/2641 | 1545/1869 | 515/622 | chr7 | 76503581 | ||
| chr7:76505412
|
C | T | 2 | a0004c0006a0004c0024 | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
synonymous_variant | LOW | c.1680C>T | p.Leu560Leu | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 2062/2641 | 1680/1869 | 560/622 | chr7 | 76505412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76463617
|
A | G | 1 | a0002c0008t0004 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-182A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/11 | 16893 | chr7 | 76463617 | |||||
| chr7:76480450
|
G | A | 1 | a0001c0023t0006 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/11 | 60 | chr7 | 76480450 | |||||
| chr7:76480466
|
G | A | 1 | a0002c0002t0007 | 1 | HG02293.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/11 | 44 | chr7 | 76480466 | |||||
| chr7:76505612
|
C | G | 1 | a0001c0018t0011 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 11 | chr7 | 76505612 | |||||
| chr7:76505735
|
C | G | 1 | a0002c0002t0005 | 2 | HG00735.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 134 | chr7 | 76505735 | |||||
| chr7:76505735
|
C | T | 1 | a0001c0001t0010 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 134 | chr7 | 76505735 | |||||
| chr7:76505817
|
G | A | 7 | a0001c0001t0002a0001c0001t0010a0001c0018t0011others(4): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*216G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 216 | chr7 | 76505817 | |||||
| chr7:76505846
|
G | A | 1 | a0005c0009t0008 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 245 | chr7 | 76505846 | |||||
| chr7:76505922
|
G | A | 3 | a0001c0023t0006a0002c0011t0003a0010c0030t0003 | 4 | HG02451.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 321 | chr7 | 76505922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76462005
|
G | T | 93 | a0001c0003t0001g0219a0001c0003t0001g0220a0001c0003t0001g0266others(90): Show | 94 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-255+169G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462005 | ||||||
| chr7:76462045
|
C | A | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-255+209C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462045 | ||||||
| chr7:76462317
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-255+481C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462317 | ||||||
| chr7:76462599
|
A | G | 2 | a0002c0007t0001g0275a0002c0007t0001g0276 | 2 | HG00609.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-255+763A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462599 | ||||||
| chr7:76462814
|
C | T | 25 | a0001c0001t0002g0003a0001c0001t0002g0161a0001c0001t0002g0165others(22): Show | 26 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.-254-731C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462814 | ||||||
| chr7:76462926
|
G | T | 1 | a0001c0001t0002g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-254-619G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462926 | ||||||
| chr7:76463044
|
G | C | 1 | a0002c0002t0005g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-254-501G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463044 | ||||||
| chr7:76463062
|
G | A | 1 | a0002c0007t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-254-483G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463062 | ||||||
| chr7:76463089
|
TAAA | T | 139 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(136): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-254-451_-254-449d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 76463089 | |||||
| chr7:76463101
|
CT | C | 8 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(5): Show | 8 | HG00673.hp2 HG01256.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.-254-430delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 76463101 | |||||
| chr7:76463152
|
C | G | 1 | a0002c0002t0005g0274 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-254-393C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463152 | ||||||
| chr7:76463192
|
A | G | 8 | a0001c0031t0001g0273a0002c0007t0001g0268a0002c0007t0001g0270others(5): Show | 8 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.-254-353A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463192 | ||||||
| chr7:76463206
|
A | G | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-254-339A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463206 | ||||||
| chr7:76463210
|
G | A | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-254-335G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463210 | ||||||
| chr7:76463309
|
A | G | 1 | a0004c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-254-236A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463309 | ||||||
| chr7:76463401
|
C | G | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-254-144C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463401 | ||||||
| chr7:76463747
|
A | G | 6 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(3): Show | 6 | HG00735.hp2 HG02451.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+38A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76463747 | ||||||
| chr7:76463779
|
G | C | 1 | a0003c0004t0001g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-90+70G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76463779 | ||||||
| chr7:76463838
|
C | G | 2 | a0001c0003t0001g0158a0003c0004t0001g0262 | 2 | HG01175.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-90+129C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76463838 | ||||||
| chr7:76463984
|
T | C | 1 | a0002c0002t0001g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-90+275T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76463984 | ||||||
| chr7:76464017
|
G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-90+308G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464017 | ||||||
| chr7:76464152
|
G | T | 1 | a0001c0003t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-90+443G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464152 | ||||||
| chr7:76464222
|
G | A | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+513G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464222 | ||||||
| chr7:76464245
|
A | G | 143 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(140): Show | 144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-90+536A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464245 | ||||||
| chr7:76464263
|
C | T | 2 | a0001c0001t0002g0109a0001c0001t0002g0110 | 2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-90+554C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464263 | ||||||
| chr7:76464264
|
G | A | 11 | a0001c0003t0001g0116a0004c0006t0001g0115a0004c0006t0001g0117others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+555G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464264 | ||||||
| chr7:76464316
|
T | G | 3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+607T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464316 | ||||||
| chr7:76464394
|
G | A | 1 | a0001c0001t0002g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-90+685G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464394 | ||||||
| chr7:76464420
|
CT | C | 49 | a0001c0003t0001g0219a0001c0003t0001g0220a0001c0013t0001g0224others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90+712delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464420 | ||||||
| chr7:76464421
|
T | C | 110 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(107): Show | 110 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.-90+712T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464421 | ||||||
| chr7:76464698
|
C | T | 128 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(125): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-90+989C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464698 | ||||||
| chr7:76464715
|
T | A | 5 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(2): Show | 5 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+1006T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464715 | ||||||
| chr7:76464759
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-90+1050C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464759 | ||||||
| chr7:76464777
|
TTACA | T | 16 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-90+1074_-90+1077d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76464777 | |||||
| chr7:76464833
|
C | T | 1 | a0003c0004t0001g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-90+1124C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464833 | ||||||
| chr7:76464859
|
A | G | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-90+1150A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464859 | ||||||
| chr7:76464867
|
A | G | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+1158A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464867 | ||||||
| chr7:76464971
|
T | C | 237 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(234): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-90+1262T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464971 | ||||||
| chr7:76465038
|
A | C | 13 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-90+1329A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465038 | ||||||
| chr7:76465044
|
T | G | 5 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(2): Show | 5 | HG02451.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+1335T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465044 | ||||||
| chr7:76465136
|
A | G | 17 | a0001c0001t0002g0079a0001c0001t0002g0111a0001c0001t0002g0112others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-90+1427A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465136 | ||||||
| chr7:76465224
|
G | A | 4 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(1): Show | 4 | HG00597.hp2 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+1515G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465224 | ||||||
| chr7:76465227
|
A | G | 145 | a0001c0001t0002g0108a0001c0001t0002g0111a0001c0001t0002g0112others(142): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.-90+1518A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465227 | ||||||
| chr7:76465462
|
A | G | 263 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-90+1753A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465462 | ||||||
| chr7:76465471
|
C | T | 206 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(203): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-90+1762C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465471 | ||||||
| chr7:76465501
|
C | T | 1 | a0003c0004t0001g0257 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-90+1792C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465501 | ||||||
| chr7:76465661
|
A | G | 11 | a0001c0001t0002g0107a0001c0001t0002g0111a0001c0001t0002g0112others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+1952A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465661 | ||||||
| chr7:76465673
|
C | T | 110 | a0001c0003t0001g0116a0001c0003t0001g0157a0001c0003t0001g0219others(107): Show | 111 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-90+1964C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465673 | ||||||
| chr7:76465712
|
C | G | 27 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(24): Show | 27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.-90+2003C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465712 | ||||||
| chr7:76465769
|
C | T | 2 | a0002c0032t0001g0256a0003c0005t0001g0024 | 2 | HG00733.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-90+2060C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465769 | ||||||
| chr7:76465860
|
C | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-90+2151C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465860 | ||||||
| chr7:76465886
|
G | T | 1 | a0001c0001t0002g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-90+2177G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465886 | ||||||
| chr7:76465984
|
C | T | 1 | a0001c0003t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-90+2275C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465984 | ||||||
| chr7:76465991
|
C | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-90+2282C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465991 | ||||||
| chr7:76466019
|
C | T | 11 | a0001c0003t0001g0116a0004c0006t0001g0115a0004c0006t0001g0117others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+2310C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466019 | ||||||
| chr7:76466268
|
G | A | 11 | a0001c0003t0001g0116a0004c0006t0001g0115a0004c0006t0001g0117others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+2559G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466268 | ||||||
| chr7:76466351
|
C | T | 6 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(3): Show | 6 | HG02071.hp1 HG02451.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90+2642C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466351 | ||||||
| chr7:76466413
|
C | CT | 139 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(136): Show | 140 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.-90+2714dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76466413 | |||||
| chr7:76466592
|
CT | C | 49 | a0001c0001t0002g0012a0001c0003t0001g0128a0001c0003t0001g0129others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.-90+2895delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76466592 | |||||
| chr7:76466592
|
CTT | C | 9 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0001g0138others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+2894_-90+2895d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76466592 | |||||
| chr7:76466631
|
G | A | 2 | a0001c0001t0002g0183a0002c0020t0009g0011 | 2 | HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+2922G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466631 | ||||||
| chr7:76466660
|
C | T | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-90+2951C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466660 | ||||||
| chr7:76466678
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-90+2969A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466678 | ||||||
| chr7:76466690
|
C | A | 1 | a0002c0002t0001g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-90+2981C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466690 | ||||||
| chr7:76466713
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-90+3004C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466713 | ||||||
| chr7:76466722
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-90+3013C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466722 | ||||||
| chr7:76466743
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-90+3034C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466743 | ||||||
| chr7:76466786
|
C | T | 11 | a0001c0003t0001g0116a0004c0006t0001g0115a0004c0006t0001g0117others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+3077C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466786 | ||||||
| chr7:76466787
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-90+3078G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466787 | ||||||
| chr7:76466836
|
G | T | 11 | a0001c0003t0001g0116a0004c0006t0001g0115a0004c0006t0001g0117others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+3127G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466836 | ||||||
| chr7:76466844
|
T | C | 3 | a0001c0001t0002g0183a0001c0003t0001g0158a0002c0020t0009g0011 | 3 | HG01175.hp2 HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3135T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466844 | ||||||
| chr7:76466877
|
T | C | 3 | a0001c0001t0002g0183a0001c0003t0001g0158a0002c0020t0009g0011 | 3 | HG01175.hp2 HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3168T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466877 | ||||||
| chr7:76466888
|
G | A | 2 | a0001c0001t0002g0183a0002c0020t0009g0011 | 2 | HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3179G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466888 | ||||||
| chr7:76466929
|
A | G | 2 | a0001c0001t0002g0183a0002c0020t0009g0011 | 2 | HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3220A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466929 | ||||||
| chr7:76466945
|
A | G | 1 | a0014c0016t0001g0227 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-90+3236A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466945 | ||||||
| chr7:76466964
|
A | G | 2 | a0001c0001t0002g0183a0002c0020t0009g0011 | 2 | HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3255A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466964 | ||||||
| chr7:76466980
|
C | T | 1 | a0003c0004t0001g0255 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-90+3271C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466980 | ||||||
| chr7:76466981
|
G | A | 1 | a0002c0002t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-90+3272G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466981 | ||||||
| chr7:76467097
|
C | T | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-90+3388C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467097 | ||||||
| chr7:76467106
|
C | G | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-90+3397C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467106 | ||||||
| chr7:76467116
|
C | G | 32 | a0001c0001t0002g0077a0001c0001t0002g0078a0001c0001t0002g0183others(29): Show | 32 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.-90+3407C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467116 | ||||||
| chr7:76467143
|
C | G | 1 | a0001c0003t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-90+3434C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467143 | ||||||
| chr7:76467145
|
C | T | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-90+3436C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467145 | ||||||
| chr7:76467189
|
A | G | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-90+3480A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467189 | ||||||
| chr7:76467229
|
A | G | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-90+3520A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467229 | ||||||
| chr7:76467241
|
T | A | 142 | a0001c0001t0002g0183a0001c0003t0001g0116a0001c0003t0001g0128others(139): Show | 143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.-90+3532T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467241 | ||||||
| chr7:76467243
|
G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-90+3534G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467243 | ||||||
| chr7:76467376
|
G | A | 1 | a0002c0008t0004g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+3667G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467376 | ||||||
| chr7:76467384
|
G | A | 129 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(126): Show | 130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-90+3675G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467384 | ||||||
| chr7:76467447
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-90+3738C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467447 | ||||||
| chr7:76467733
|
A | C | 6 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+4024A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467733 | ||||||
| chr7:76467746
|
G | C | 11 | a0001c0003t0001g0116a0004c0006t0001g0115a0004c0006t0001g0117others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+4037G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467746 | ||||||
| chr7:76467750
|
C | T | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-90+4041C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467750 | ||||||
| chr7:76467799
|
G | A | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-90+4090G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467799 | ||||||
| chr7:76467897
|
C | T | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-90+4188C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467897 | ||||||
| chr7:76467904
|
C | A | 1 | a0001c0003t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-90+4195C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467904 | ||||||
| chr7:76468028
|
T | C | 1 | a0010c0030t0003g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-90+4319T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468028 | ||||||
| chr7:76468140
|
G | A | 1 | a0001c0001t0010g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-90+4431G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468140 | ||||||
| chr7:76468178
|
G | A | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90+4469G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468178 | ||||||
| chr7:76468438
|
GCCC | G | 99 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(96): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-90+4730_-90+4732d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468438 | ||||||
| chr7:76468447
|
C | CT | 6 | a0001c0001t0002g0084a0001c0001t0002g0085a0002c0011t0003g0264others(3): Show | 6 | HG00733.hp1 HG01891.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+4738_-90+4739i others(3): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468447
|
CA | C | 15 | a0001c0003t0001g0219a0001c0003t0001g0220a0001c0003t0001g0266others(12): Show | 15 | HG00735.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-90+4739delA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468447
|
CAT | C | 36 | a0002c0002t0001g0004a0002c0002t0001g0126a0002c0002t0001g0127others(33): Show | 37 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4740d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468447
|
CATTT | C | 11 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076others(8): Show | 11 | HG01192.hp2 HG01993.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4742d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468447
|
CATTTT | C | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4743d others(7): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468447
|
CATTTTT | C | 5 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG01167.hp1 HG02080.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4744d others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468447
|
CATTTTTT | C | 11 | a0001c0003t0001g0116a0004c0006t0001g0115a0004c0006t0001g0117others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4745d others(9): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468447
|
CATTTTTT others(5): Show |
C | 57 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4750d others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468447
|
CATTTTTT others(6): Show |
C | 13 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4751d others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | ||||||
| chr7:76468448
|
A | AT | 8 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0102others(5): Show | 8 | HG00741.hp2 HG01106.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+4767dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468448 | |||||
| chr7:76468448
|
A | T | 9 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(6): Show | 9 | HG00733.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-90+4739A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468448 | ||||||
| chr7:76468561
|
A | T | 7 | a0004c0006t0001g0115a0004c0006t0001g0119a0004c0006t0001g0120others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90+4852A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468561 | ||||||
| chr7:76468578
|
C | T | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+4869C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468578 | ||||||
| chr7:76468677
|
C | T | 58 | a0001c0003t0001g0219a0001c0003t0001g0220a0001c0003t0001g0266others(55): Show | 59 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-90+4968C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468677 | ||||||
| chr7:76468758
|
A | ATT | 8 | a0001c0003t0001g0138a0001c0003t0001g0140a0001c0003t0001g0141others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+5070_-90+5071d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTT | 32 | a0001c0003t0001g0219a0001c0003t0001g0220a0002c0002t0001g0004others(29): Show | 33 | HG00280.hp2 HG00558.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-90+5068_-90+5071d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTT | 19 | a0002c0002t0001g0125a0002c0002t0001g0187a0002c0002t0001g0190others(16): Show | 19 | HG00423.hp1 HG00673.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-90+5067_-90+5071d others(7): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0265others(2): Show | 5 | HG02965.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+5065_-90+5071d others(9): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(1): Show |
14 | a0001c0001t0002g0111a0001c0003t0001g0116a0002c0007t0001g0259others(11): Show | 14 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-90+5064_-90+5071d others(10): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(2): Show |
10 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114others(7): Show | 10 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90+5063_-90+5071d others(11): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(3): Show |
14 | a0003c0004t0001g0234a0003c0004t0001g0235a0003c0004t0001g0236others(11): Show | 14 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-90+5062_-90+5071d others(12): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(4): Show |
15 | a0003c0004t0001g0189a0003c0004t0001g0246a0003c0004t0001g0247others(12): Show | 15 | HG00735.hp1 HG01175.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-90+5061_-90+5071d others(13): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(5): Show |
1 | a0003c0004t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90+5060_-90+5071d others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(12): Show |
1 | a0001c0003t0001g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-90+5053_-90+5071d others(21): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(13): Show |
3 | a0001c0003t0001g0144a0001c0003t0001g0145a0001c0003t0001g0146 | 3 | HG02647.hp1 HG03139.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-90+5052_-90+5071d others(22): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(14): Show |
11 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(8): Show | 11 | HG00408.hp1 HG00597.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+5051_-90+5071d others(23): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(15): Show |
1 | a0001c0003t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-90+5050_-90+5071d others(24): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(19): Show |
1 | a0001c0003t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-90+5071_-90+5072i others(28): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
A | ATTTTTTT others(20): Show |
1 | a0001c0003t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-90+5071_-90+5072i others(29): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468758
|
AT | A | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(74): Show | 80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-90+5071delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | |||||
| chr7:76468797
|
CTG | C | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+5090_-90+5091d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468797 | |||||
| chr7:76468800
|
T | C | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+5091T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468800 | ||||||
| chr7:76468825
|
C | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034 | 3 | HG00140.hp1 HG01346.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-90+5116C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468825 | ||||||
| chr7:76468832
|
G | A | 28 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0235others(25): Show | 28 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-90+5123G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468832 | ||||||
| chr7:76469017
|
A | G | 133 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(130): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.-90+5308A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469017 | ||||||
| chr7:76469051
|
T | C | 144 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(141): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-90+5342T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469051 | ||||||
| chr7:76469133
|
T | C | 144 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(141): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-90+5424T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469133 | ||||||
| chr7:76469166
|
A | G | 3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+5457A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469166 | ||||||
| chr7:76469221
|
A | G | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+5512A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469221 | ||||||
| chr7:76469330
|
C | T | 144 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(141): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-90+5621C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469330 | ||||||
| chr7:76469359
|
G | GAT | 62 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.-90+5651_-90+5652d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469359 | |||||
| chr7:76469360
|
A | AT | 7 | a0001c0001t0002g0031a0001c0001t0002g0108a0001c0001t0002g0180others(4): Show | 7 | HG00741.hp1 HG01361.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90+5671dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469360 | |||||
| chr7:76469360
|
A | ATAT | 5 | a0001c0003t0001g0142a0002c0011t0003g0264a0003c0004t0001g0257others(2): Show | 5 | HG01243.hp2 HG02135.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+5652_-90+5653i others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469360 | |||||
| chr7:76469360
|
A | ATTT | 11 | a0001c0003t0001g0116a0004c0006t0001g0115a0004c0006t0001g0117others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+5669_-90+5671d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469360 | |||||
| chr7:76469361
|
T | TA | 49 | a0001c0003t0001g0219a0001c0003t0001g0220a0001c0003t0001g0266others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90+5652_-90+5653i others(3): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469361 | ||||||
| chr7:76469362
|
T | A | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90+5653T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469362 | ||||||
| chr7:76469381
|
A | T | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-90+5672A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469381 | ||||||
| chr7:76469394
|
CTT | C | 139 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(136): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-90+5700_-90+5701d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469394 | |||||
| chr7:76469413
|
G | A | 1 | a0003c0004t0001g0234 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-90+5704G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469413 | ||||||
| chr7:76469415
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-90+5706C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469415 | ||||||
| chr7:76469416
|
G | A | 17 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0181others(14): Show | 17 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+5707G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469416 | ||||||
| chr7:76469425
|
T | C | 144 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(141): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-90+5716T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469425 | ||||||
| chr7:76469481
|
T | G | 19 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(16): Show | 19 | HG00639.hp2 HG01192.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-90+5772T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469481 | ||||||
| chr7:76469503
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-90+5794C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469503 | ||||||
| chr7:76469507
|
C | T | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+5798C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469507 | ||||||
| chr7:76469548
|
A | G | 1 | a0001c0013t0001g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90+5839A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469548 | ||||||
| chr7:76469550
|
A | G | 1 | a0001c0013t0001g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90+5841A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469550 | ||||||
| chr7:76469552
|
T | C | 1 | a0001c0013t0001g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90+5843T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469552 | ||||||
| chr7:76469670
|
G | A | 1 | a0001c0001t0010g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-90+5961G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469670 | ||||||
| chr7:76469763
|
C | T | 3 | a0002c0002t0001g0193a0002c0002t0001g0209a0002c0002t0001g0222 | 3 | HG02622.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-90+6054C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469763 | ||||||
| chr7:76469766
|
C | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-90+6057C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469766 | ||||||
| chr7:76469856
|
T | G | 1 | a0003c0004t0001g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-90+6147T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469856 | ||||||
| chr7:76469908
|
A | T | 53 | a0001c0003t0001g0219a0001c0003t0001g0220a0001c0013t0001g0224others(50): Show | 54 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-90+6199A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469908 | ||||||
| chr7:76469937
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-90+6228A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469937 | ||||||
| chr7:76470121
|
A | C | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+6412A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470121 | ||||||
| chr7:76470159
|
G | A | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-90+6450G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470159 | ||||||
| chr7:76470243
|
T | C | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-90+6534T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470243 | ||||||
| chr7:76470308
|
A | G | 4 | a0003c0005t0001g0013a0003c0005t0001g0014a0003c0005t0001g0018others(1): Show | 4 | HG02818.hp2 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+6599A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470308 | ||||||
| chr7:76470409
|
G | A | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-90+6700G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470409 | ||||||
| chr7:76470661
|
T | G | 28 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0235others(25): Show | 28 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-90+6952T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470661 | ||||||
| chr7:76470713
|
G | A | 1 | a0002c0002t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-90+7004G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470713 | ||||||
| chr7:76470878
|
G | C | 49 | a0001c0003t0001g0219a0001c0003t0001g0220a0001c0013t0001g0224others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90+7169G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470878 | ||||||
| chr7:76470907
|
T | C | 31 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(28): Show | 31 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-90+7198T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470907 | ||||||
| chr7:76471154
|
T | G | 76 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(73): Show | 77 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-90+7445T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471154 | ||||||
| chr7:76471156
|
C | CT | 72 | a0001c0001t0002g0012a0001c0001t0002g0071a0001c0001t0002g0072others(69): Show | 73 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-90+7470dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | |||||
| chr7:76471156
|
C | CTT | 34 | a0002c0002t0001g0125a0002c0002t0001g0190a0002c0002t0001g0208others(31): Show | 34 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-90+7469_-90+7470d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | |||||
| chr7:76471156
|
C | CTTT | 6 | a0002c0008t0001g0229a0002c0008t0001g0230a0003c0004t0001g0252others(3): Show | 6 | HG00639.hp1 HG01109.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+7468_-90+7470d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | |||||
| chr7:76471156
|
CT | C | 10 | a0001c0001t0002g0035a0001c0001t0002g0038a0001c0001t0002g0083others(7): Show | 10 | HG01070.hp1 HG01167.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-90+7470delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | |||||
| chr7:76471156
|
CTTT | C | 25 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(22): Show | 25 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-90+7468_-90+7470d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | |||||
| chr7:76471184
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-90+7475C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471184 | ||||||
| chr7:76471200
|
C | T | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+7491C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471200 | ||||||
| chr7:76471209
|
T | G | 1 | a0001c0001t0002g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-90+7500T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471209 | ||||||
| chr7:76471218
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-90+7509G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471218 | ||||||
| chr7:76471287
|
T | A | 135 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(132): Show | 136 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-90+7578T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471287 | ||||||
| chr7:76471322
|
C | T | 137 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(134): Show | 138 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.-90+7613C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471322 | ||||||
| chr7:76471350
|
A | G | 1 | a0002c0002t0001g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-90+7641A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471350 | ||||||
| chr7:76471352
|
A | G | 8 | a0002c0002t0001g0187a0002c0002t0001g0192a0002c0002t0001g0207others(5): Show | 8 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90+7643A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471352 | ||||||
| chr7:76471363
|
A | G | 1 | a0002c0002t0001g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-90+7654A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471363 | ||||||
| chr7:76471434
|
T | A | 4 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(1): Show | 4 | HG00597.hp2 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+7725T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471434 | ||||||
| chr7:76471452
|
C | T | 28 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(25): Show | 28 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-90+7743C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471452 | ||||||
| chr7:76471540
|
T | G | 24 | a0001c0001t0002g0107a0001c0003t0001g0266a0001c0003t0001g0267others(21): Show | 24 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.-90+7831T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471540 | ||||||
| chr7:76471622
|
G | A | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+7913G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471622 | ||||||
| chr7:76471726
|
G | A | 1 | a0002c0002t0005g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-90+8017G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471726 | ||||||
| chr7:76471822
|
C | T | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+8113C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471822 | ||||||
| chr7:76472035
|
C | T | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-90+8326C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472035 | ||||||
| chr7:76472122
|
GGTTT | G | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-8295_-89-8292d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76472122 | |||||
| chr7:76472156
|
G | T | 15 | a0001c0023t0006g0023a0003c0005t0001g0013a0003c0005t0001g0014others(12): Show | 15 | HG00639.hp2 HG01192.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-89-8265G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472156 | ||||||
| chr7:76472171
|
C | T | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-8250C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472171 | ||||||
| chr7:76472210
|
A | G | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-8211A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472210 | ||||||
| chr7:76472225
|
C | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0177 | 2 | HG00733.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-89-8196C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472225 | ||||||
| chr7:76472236
|
G | T | 29 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(26): Show | 29 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-89-8185G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472236 | ||||||
| chr7:76472323
|
A | C | 135 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0063others(132): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-89-8098A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472323 | ||||||
| chr7:76472382
|
G | A | 239 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(236): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-89-8039G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472382 | ||||||
| chr7:76472412
|
C | T | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-8009C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472412 | ||||||
| chr7:76472436
|
C | A | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-7985C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472436 | ||||||
| chr7:76472447
|
T | C | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-7974T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472447 | ||||||
| chr7:76472482
|
A | G | 44 | a0002c0002t0001g0004a0002c0002t0001g0125a0002c0002t0001g0126others(41): Show | 45 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-89-7939A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472482 | ||||||
| chr7:76472602
|
A | G | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-89-7819A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472602 | ||||||
| chr7:76472750
|
T | A | 1 | a0001c0001t0002g0167 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-89-7671T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472750 | ||||||
| chr7:76472887
|
G | A | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-7534G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472887 | ||||||
| chr7:76472892
|
A | C | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-7529A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472892 | ||||||
| chr7:76472903
|
A | G | 130 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(127): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-89-7518A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472903 | ||||||
| chr7:76472996
|
C | T | 1 | a0001c0003t0001g0131 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-89-7425C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472996 | ||||||
| chr7:76473162
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-89-7259T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473162 | ||||||
| chr7:76473400
|
T | C | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-7021T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473400 | ||||||
| chr7:76473574
|
A | G | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-6847A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473574 | ||||||
| chr7:76473607
|
C | T | 28 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0235others(25): Show | 28 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-89-6814C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473607 | ||||||
| chr7:76473826
|
A | G | 2 | a0003c0005t0001g0016a0003c0005t0001g0017 | 2 | HG00639.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-89-6595A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473826 | ||||||
| chr7:76473898
|
G | A | 130 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(127): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-89-6523G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473898 | ||||||
| chr7:76473919
|
CT | C | 128 | a0001c0001t0002g0009a0001c0001t0002g0181a0001c0003t0001g0116others(125): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-89-6483delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76473919 | |||||
| chr7:76473959
|
T | C | 1 | a0011c0019t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-89-6462T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473959 | ||||||
| chr7:76474082
|
C | T | 13 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-6339C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474082 | ||||||
| chr7:76474141
|
A | G | 1 | a0001c0003t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-89-6280A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474141 | ||||||
| chr7:76474146
|
C | G | 1 | a0001c0003t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-89-6275C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474146 | ||||||
| chr7:76474148
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-6273C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474148 | ||||||
| chr7:76474163
|
C | T | 6 | a0001c0001t0002g0037a0001c0001t0002g0060a0001c0001t0002g0061others(3): Show | 6 | HG01496.hp1 HG01934.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-6258C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474163 | ||||||
| chr7:76474181
|
T | TTTTTTC | 24 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(21): Show | 24 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-89-6217_-89-6212d others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76474181 | |||||
| chr7:76474181
|
TTTTTTCT others(5): Show |
T | 57 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-89-6223_-89-6212d others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76474181 | |||||
| chr7:76474223
|
CT | C | 116 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0038others(113): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-89-6185delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76474223 | |||||
| chr7:76474223
|
CTT | C | 28 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0235others(25): Show | 28 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-89-6186_-89-6185d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76474223 | |||||
| chr7:76474278
|
C | T | 2 | a0002c0002t0001g0186a0002c0002t0001g0213 | 2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-89-6143C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474278 | ||||||
| chr7:76474279
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0002g0097 | 2 | HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-89-6142G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474279 | ||||||
| chr7:76474507
|
G | C | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-5914G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474507 | ||||||
| chr7:76474514
|
A | G | 49 | a0001c0003t0001g0116a0001c0003t0001g0219a0001c0003t0001g0220others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-89-5907A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474514 | ||||||
| chr7:76474515
|
G | T | 60 | a0001c0003t0001g0116a0001c0003t0001g0156a0001c0003t0001g0219others(57): Show | 61 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-89-5906G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474515 | ||||||
| chr7:76474563
|
C | G | 5 | a0001c0003t0001g0116a0001c0003t0001g0140a0001c0003t0001g0141others(2): Show | 5 | HG02723.hp2 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-89-5858C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474563 | ||||||
| chr7:76474864
|
G | T | 50 | a0001c0003t0001g0116a0001c0003t0001g0158a0001c0003t0001g0219others(47): Show | 51 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-89-5557G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474864 | ||||||
| chr7:76474906
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-5515C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474906 | ||||||
| chr7:76475069
|
G | T | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-89-5352G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475069 | ||||||
| chr7:76475097
|
A | T | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-89-5324A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475097 | ||||||
| chr7:76475183
|
T | A | 14 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(11): Show | 14 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89-5238T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475183 | ||||||
| chr7:76475226
|
A | G | 271 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(268): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-89-5195A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475226 | ||||||
| chr7:76475226
|
A | T | 1 | a0001c0001t0002g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-89-5195A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475226 | ||||||
| chr7:76475243
|
G | A | 9 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0001g0138others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-5178G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475243 | ||||||
| chr7:76475259
|
C | T | 1 | a0002c0011t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-89-5162C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475259 | ||||||
| chr7:76475271
|
A | G | 49 | a0001c0003t0001g0116a0001c0003t0001g0219a0001c0003t0001g0220others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-89-5150A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475271 | ||||||
| chr7:76475456
|
G | A | 130 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(127): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-89-4965G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475456 | ||||||
| chr7:76475510
|
A | T | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-4911A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475510 | ||||||
| chr7:76475513
|
C | G | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-4908C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475513 | ||||||
| chr7:76475515
|
C | A | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-4906C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475515 | ||||||
| chr7:76475515
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-89-4906C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475515 | ||||||
| chr7:76475519
|
T | A | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-4902T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475519 | ||||||
| chr7:76475553
|
G | C | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-89-4868G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475553 | ||||||
| chr7:76475574
|
C | T | 14 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(11): Show | 14 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89-4847C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475574 | ||||||
| chr7:76475701
|
GA | G | 101 | a0001c0003t0001g0116a0001c0003t0001g0219a0001c0003t0001g0220others(98): Show | 102 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-89-4712delA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76475701 | |||||
| chr7:76475701
|
GAA | G | 29 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(26): Show | 29 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-89-4713_-89-4712d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76475701 | |||||
| chr7:76476000
|
A | G | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-89-4421A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476000 | ||||||
| chr7:76476017
|
G | A | 51 | a0001c0003t0001g0116a0001c0003t0001g0219a0001c0003t0001g0220others(48): Show | 52 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-89-4404G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476017 | ||||||
| chr7:76476021
|
C | T | 139 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(136): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-89-4400C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476021 | ||||||
| chr7:76476095
|
T | G | 28 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0235others(25): Show | 28 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-89-4326T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476095 | ||||||
| chr7:76476156
|
T | C | 1 | a0005c0009t0002g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-89-4265T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476156 | ||||||
| chr7:76476186
|
A | G | 1 | a0001c0003t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-89-4235A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476186 | ||||||
| chr7:76476227
|
G | C | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-4194G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476227 | ||||||
| chr7:76476402
|
T | C | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-4019T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476402 | ||||||
| chr7:76476540
|
T | C | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0011t0003g0264others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-3881T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476540 | ||||||
| chr7:76476748
|
T | A | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-89-3673T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476748 | ||||||
| chr7:76476771
|
C | T | 1 | a0005c0009t0002g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-89-3650C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476771 | ||||||
| chr7:76476871
|
T | C | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-3550T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476871 | ||||||
| chr7:76476872
|
G | A | 131 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(128): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-89-3549G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476872 | ||||||
| chr7:76476895
|
G | A | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-3526G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476895 | ||||||
| chr7:76477041
|
G | A | 2 | a0001c0003t0001g0146a0001c0003t0001g0154 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-89-3380G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477041 | ||||||
| chr7:76477157
|
C | CGCCCGCC others(1): Show |
87 | a0001c0003t0001g0116a0001c0003t0001g0219a0001c0003t0001g0220others(84): Show | 88 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-89-3257_-89-3256i others(10): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477157 | |||||
| chr7:76477189
|
C | T | 13 | a0003c0004t0001g0242a0003c0004t0001g0243a0003c0004t0001g0251others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-3232C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477189 | ||||||
| chr7:76477194
|
C | T | 2 | a0004c0006t0001g0117a0004c0006t0001g0118 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-89-3227C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477194 | ||||||
| chr7:76477195
|
A | G | 13 | a0003c0004t0001g0242a0003c0004t0001g0243a0003c0004t0001g0251others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-3226A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477195 | ||||||
| chr7:76477231
|
G | A | 3 | a0001c0003t0001g0146a0001c0003t0001g0154a0001c0003t0001g0158 | 3 | HG01175.hp2 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-89-3190G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477231 | ||||||
| chr7:76477235
|
C | T | 137 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(134): Show | 138 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.-89-3186C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477235 | ||||||
| chr7:76477244
|
C | T | 138 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(135): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-89-3177C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477244 | ||||||
| chr7:76477273
|
G | A | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-3148G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477273 | ||||||
| chr7:76477378
|
T | G | 64 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(61): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-89-3043T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477378 | ||||||
| chr7:76477499
|
T | C | 13 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-2922T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477499 | ||||||
| chr7:76477537
|
A | C | 3 | a0001c0001t0002g0012a0001c0001t0002g0095a0001c0003t0001g0158 | 3 | HG01175.hp2 NA18961.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-89-2884A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477537 | ||||||
| chr7:76477602
|
A | G | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-89-2819A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477602 | ||||||
| chr7:76477666
|
C | A | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-2755C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477666 | ||||||
| chr7:76477728
|
A | G | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-2693A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477728 | ||||||
| chr7:76477800
|
C | CTAAA | 16 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0029others(13): Show | 17 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-89-2583_-89-2580d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | |||||
| chr7:76477800
|
C | CTAAATAA others(1): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0089a0001c0001t0002g0168 | 3 | NA18959.hp1 NA18959.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-89-2587_-89-2580d others(10): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | |||||
| chr7:76477800
|
CTAAA | C | 9 | a0001c0001t0002g0184a0001c0003t0001g0128a0001c0003t0001g0138others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-2583_-89-2580d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | |||||
| chr7:76477800
|
CTAAATAA others(1): Show |
C | 116 | a0001c0001t0002g0110a0001c0003t0001g0116a0001c0003t0001g0129others(113): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-89-2587_-89-2580d others(10): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | |||||
| chr7:76477800
|
CTAAATAA others(5): Show |
C | 9 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0003t0001g0266others(6): Show | 9 | HG02165.hp1 HG02897.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-2591_-89-2580d others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | |||||
| chr7:76477800
|
CTAAATAA others(9): Show |
C | 13 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-2595_-89-2580d others(18): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | |||||
| chr7:76477991
|
C | T | 1 | a0001c0013t0001g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-89-2430C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477991 | ||||||
| chr7:76478093
|
G | A | 7 | a0004c0006t0001g0115a0004c0006t0001g0119a0004c0006t0001g0120others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-89-2328G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478093 | ||||||
| chr7:76478229
|
G | A | 49 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-89-2192G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478229 | ||||||
| chr7:76478231
|
A | G | 59 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(56): Show | 60 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-89-2190A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478231 | ||||||
| chr7:76478414
|
A | AT | 28 | a0001c0001t0002g0058a0001c0001t0002g0103a0001c0001t0002g0104others(25): Show | 28 | HG00597.hp1 HG00741.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-89-1988dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76478414 | |||||
| chr7:76478414
|
AT | A | 8 | a0001c0001t0002g0089a0001c0001t0002g0167a0001c0003t0001g0116others(5): Show | 8 | HG01884.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-89-1988delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76478414 | |||||
| chr7:76478457
|
C | T | 6 | a0001c0001t0002g0106a0001c0003t0001g0266a0001c0003t0001g0267others(3): Show | 6 | HG01192.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-1964C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478457 | ||||||
| chr7:76478514
|
G | T | 3 | a0003c0004t0001g0241a0003c0004t0001g0250a0003c0004t0001g0254 | 3 | HG00735.hp1 HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-89-1907G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478514 | ||||||
| chr7:76478568
|
G | A | 1 | a0002c0002t0001g0197 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-89-1853G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478568 | ||||||
| chr7:76478613
|
A | G | 49 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0039others(46): Show | 49 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-89-1808A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478613 | ||||||
| chr7:76478658
|
C | T | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-89-1763C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478658 | ||||||
| chr7:76478662
|
C | G | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-89-1759C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478662 | ||||||
| chr7:76478662
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-89-1759C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478662 | ||||||
| chr7:76478687
|
G | A | 237 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(234): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-89-1734G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478687 | ||||||
| chr7:76478746
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(75): Show | 81 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-89-1675G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478746 | ||||||
| chr7:76478829
|
C | A | 3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-1592C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478829 | ||||||
| chr7:76478957
|
T | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-89-1464T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478957 | ||||||
| chr7:76478963
|
A | G | 83 | a0001c0001t0002g0106a0001c0003t0001g0266a0001c0003t0001g0267others(80): Show | 84 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-89-1458A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478963 | ||||||
| chr7:76478993
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-1428C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478993 | ||||||
| chr7:76479036
|
A | G | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-1385A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479036 | ||||||
| chr7:76479039
|
C | G | 28 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0235others(25): Show | 28 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-89-1382C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479039 | ||||||
| chr7:76479104
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-89-1317C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479104 | ||||||
| chr7:76479251
|
A | T | 92 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(89): Show | 92 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-89-1170A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479251 | ||||||
| chr7:76479262
|
G | A | 6 | a0001c0001t0002g0040a0001c0001t0002g0066a0001c0001t0002g0067others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-1159G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479262 | ||||||
| chr7:76479288
|
C | T | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-89-1133C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479288 | ||||||
| chr7:76479316
|
G | A | 11 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG02056.hp1 HG02129.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-89-1105G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479316 | ||||||
| chr7:76479395
|
A | G | 146 | a0001c0001t0010g0086a0001c0003t0001g0116a0001c0003t0001g0128others(143): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-89-1026A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479395 | ||||||
| chr7:76479508
|
A | T | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-913A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479508 | ||||||
| chr7:76479529
|
G | A | 136 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(133): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-89-892G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479529 | ||||||
| chr7:76479610
|
T | A | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-811T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479610 | ||||||
| chr7:76479641
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-89-780C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479641 | ||||||
| chr7:76479710
|
G | A | 124 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(121): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-89-711G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479710 | ||||||
| chr7:76479839
|
A | T | 1 | a0001c0001t0010g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-89-582A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479839 | ||||||
| chr7:76479873
|
G | T | 8 | a0004c0006t0001g0115a0004c0006t0001g0119a0004c0006t0001g0120others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-548G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479873 | ||||||
| chr7:76479907
|
G | A | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-89-514G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479907 | ||||||
| chr7:76479915
|
G | A | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-89-506G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479915 | ||||||
| chr7:76479924
|
G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-89-497G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479924 | ||||||
| chr7:76479964
|
G | C | 1 | a0002c0008t0004g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-89-457G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479964 | ||||||
| chr7:76480034
|
C | T | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-387C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480034 | ||||||
| chr7:76480077
|
G | A | 62 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.-89-344G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480077 | ||||||
| chr7:76480079
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-342C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480079 | ||||||
| chr7:76480099
|
G | A | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-322G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480099 | ||||||
| chr7:76480103
|
C | G | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-318C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480103 | ||||||
| chr7:76480195
|
C | T | 1 | a0004c0006t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-89-226C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480195 | ||||||
| chr7:76480227
|
A | C | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-194A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480227 | ||||||
| chr7:76480228
|
C | A | 1 | a0001c0001t0002g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-89-193C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480228 | ||||||
| chr7:76480273
|
G | C | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-89-148G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480273 | ||||||
| chr7:76480301
|
T | C | 13 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-120T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480301 | ||||||
| chr7:76480305
|
C | CA | 6 | a0001c0003t0001g0266a0001c0003t0001g0267a0002c0002t0001g0226others(3): Show | 6 | HG02056.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-101dupA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76480305 | |||||
| chr7:76480327
|
G | C | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-89-94G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480327 | ||||||
| chr7:76480342
|
G | A | 1 | a0014c0016t0001g0227 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-89-79G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480342 | ||||||
| chr7:76480396
|
C | A | 3 | a0002c0002t0001g0125a0002c0002t0001g0126a0002c0002t0001g0127 | 3 | HG01070.hp2 HG01071.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-89-25C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480396 | ||||||
| chr7:76480399
|
C | G | 1 | a0002c0011t0003g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-89-22C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480399 | ||||||
| chr7:76480812
|
T | C | 2 | a0004c0006t0001g0117a0004c0006t0001g0118 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.268+35T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76480812 | ||||||
| chr7:76480917
|
G | A | 34 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(31): Show | 34 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.268+140G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76480917 | ||||||
| chr7:76481018
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+241C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481018 | ||||||
| chr7:76481109
|
G | A | 4 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(1): Show | 4 | HG00597.hp2 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+332G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481109 | ||||||
| chr7:76481111
|
G | A | 9 | a0003c0005t0001g0015a0003c0005t0001g0016a0003c0005t0001g0017others(6): Show | 9 | HG00639.hp2 HG01192.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+334G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481111 | ||||||
| chr7:76481155
|
C | T | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.268+378C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481155 | ||||||
| chr7:76481181
|
G | A | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268+404G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481181 | ||||||
| chr7:76481189
|
CT | C | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.268+427delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 76481189 | |||||
| chr7:76481232
|
A | G | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.268+455A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481232 | ||||||
| chr7:76481251
|
G | A | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.268+474G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481251 | ||||||
| chr7:76481376
|
G | A | 1 | a0009c0015t0001g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.268+599G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481376 | ||||||
| chr7:76481385
|
C | G | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.268+608C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481385 | ||||||
| chr7:76481706
|
G | T | 49 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.269-802G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481706 | ||||||
| chr7:76481806
|
T | G | 1 | a0001c0001t0002g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.269-702T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481806 | ||||||
| chr7:76481835
|
GT | G | 128 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(125): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.269-662delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 76481835 | |||||
| chr7:76481848
|
GTGTT | G | 142 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(139): Show | 143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.269-642_269-639del others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 76481848 | |||||
| chr7:76481922
|
T | A | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.269-586T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481922 | ||||||
| chr7:76481923
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-585C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481923 | ||||||
| chr7:76481925
|
T | A | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.269-583T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481925 | ||||||
| chr7:76481953
|
C | T | 1 | a0001c0001t0002g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.269-555C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481953 | ||||||
| chr7:76481954
|
T | C | 1 | a0001c0001t0002g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.269-554T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481954 | ||||||
| chr7:76481955
|
C | A | 1 | a0001c0001t0002g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.269-553C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481955 | ||||||
| chr7:76481956
|
C | T | 13 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.269-552C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481956 | ||||||
| chr7:76481957
|
G | A | 2 | a0001c0001t0002g0105a0001c0003t0001g0136 | 2 | HG02818.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.269-551G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481957 | ||||||
| chr7:76481979
|
C | T | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.269-529C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481979 | ||||||
| chr7:76481980
|
G | A | 2 | a0001c0001t0002g0161a0001c0001t0002g0177 | 2 | HG00733.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.269-528G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481980 | ||||||
| chr7:76481980
|
G | C | 1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.269-528G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481980 | ||||||
| chr7:76482094
|
A | G | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-414A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76482094 | ||||||
| chr7:76482215
|
C | G | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.269-293C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76482215 | ||||||
| chr7:76482274
|
C | T | 1 | a0002c0011t0003g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.269-234C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76482274 | ||||||
| chr7:76483152
|
C | T | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | splice_region_variant&intron_variant | LOW | c.908+5C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483152 | ||||||
| chr7:76483163
|
G | A | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.908+16G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483163 | ||||||
| chr7:76483166
|
G | A | 1 | a0003c0005t0001g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.908+19G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483166 | ||||||
| chr7:76483170
|
G | A | 62 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.908+23G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483170 | ||||||
| chr7:76483258
|
C | T | 1 | a0002c0002t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.908+111C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483258 | ||||||
| chr7:76483300
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG00408.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.908+153C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483300 | ||||||
| chr7:76483307
|
A | G | 1 | a0010c0030t0003g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.908+160A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483307 | ||||||
| chr7:76483345
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+198C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483345 | ||||||
| chr7:76483346
|
G | A | 1 | a0010c0030t0003g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.908+199G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483346 | ||||||
| chr7:76483385
|
T | C | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.908+238T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483385 | ||||||
| chr7:76483584
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.908+437C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483584 | ||||||
| chr7:76483638
|
T | C | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.908+491T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483638 | ||||||
| chr7:76483969
|
A | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0058 | 2 | NA18999.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.908+822A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483969 | ||||||
| chr7:76484013
|
C | T | 3 | a0002c0002t0001g0193a0002c0002t0001g0209a0002c0002t0001g0222 | 3 | HG02622.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.908+866C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484013 | ||||||
| chr7:76484014
|
A | G | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.908+867A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484014 | ||||||
| chr7:76484022
|
A | G | 6 | a0001c0003t0001g0137a0001c0013t0001g0224a0002c0002t0001g0228others(3): Show | 6 | HG01081.hp2 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+875A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484022 | ||||||
| chr7:76484046
|
C | T | 131 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(128): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.908+899C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484046 | ||||||
| chr7:76484217
|
G | T | 1 | a0001c0001t0002g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.908+1070G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484217 | ||||||
| chr7:76484333
|
G | A | 145 | a0001c0001t0002g0003a0001c0001t0002g0161a0001c0001t0002g0165others(142): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.908+1186G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484333 | ||||||
| chr7:76484378
|
AC | A | 52 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0041others(49): Show | 53 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.908+1238delC | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76484378 | |||||
| chr7:76484550
|
C | T | 5 | a0001c0001t0002g0028a0002c0002t0001g0004a0002c0008t0004g0132others(2): Show | 6 | HG01256.hp2 HG01258.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.908+1403C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484550 | ||||||
| chr7:76484551
|
G | A | 17 | a0001c0001t0002g0003a0001c0001t0002g0161a0001c0001t0002g0167others(14): Show | 18 | HG00544.hp2 HG00597.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.908+1404G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484551 | ||||||
| chr7:76484579
|
G | T | 1 | a0001c0001t0002g0179 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.908+1432G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484579 | ||||||
| chr7:76484581
|
C | T | 3 | a0003c0004t0001g0235a0003c0004t0001g0240a0003c0004t0001g0261 | 3 | HG00140.hp2 HG01123.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.908+1434C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484581 | ||||||
| chr7:76484582
|
A | G | 157 | a0001c0001t0001g0088a0001c0001t0002g0003a0001c0001t0002g0038others(154): Show | 159 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.908+1435A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484582 | ||||||
| chr7:76484659
|
G | A | 39 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(36): Show | 41 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.908+1512G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484659 | ||||||
| chr7:76484685
|
G | A | 3 | a0001c0003t0001g0135a0001c0003t0001g0144a0001c0003t0001g0149 | 3 | HG00323.hp2 NA18952.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.908+1538G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484685 | ||||||
| chr7:76484719
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.908+1572C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484719 | ||||||
| chr7:76484720
|
G | T | 94 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(91): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.908+1573G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484720 | ||||||
| chr7:76484812
|
G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.908+1665G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484812 | ||||||
| chr7:76484857
|
T | G | 157 | a0001c0001t0002g0003a0001c0001t0002g0096a0001c0001t0002g0161others(154): Show | 159 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.908+1710T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484857 | ||||||
| chr7:76484879
|
C | T | 27 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(24): Show | 27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.908+1732C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484879 | ||||||
| chr7:76484904
|
C | CT | 31 | a0001c0001t0002g0003a0001c0001t0002g0161a0001c0001t0002g0165others(28): Show | 32 | HG00544.hp2 HG00597.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.908+1759dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76484904 | |||||
| chr7:76485079
|
C | A | 1 | a0002c0002t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.908+1932C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485079 | ||||||
| chr7:76485235
|
A | G | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908+2088A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485235 | ||||||
| chr7:76485253
|
A | G | 164 | a0001c0001t0002g0003a0001c0001t0002g0161a0001c0001t0002g0165others(161): Show | 166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.908+2106A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485253 | ||||||
| chr7:76485262
|
G | A | 1 | a0002c0007t0001g0260 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.908+2115G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485262 | ||||||
| chr7:76485267
|
G | T | 33 | a0001c0001t0002g0003a0001c0001t0002g0161a0001c0001t0002g0165others(30): Show | 34 | HG00544.hp2 HG00597.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.908+2120G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485267 | ||||||
| chr7:76485270
|
A | G | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.908+2123A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485270 | ||||||
| chr7:76485280
|
G | A | 1 | a0001c0001t0002g0095 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.908+2133G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485280 | ||||||
| chr7:76485311
|
T | C | 166 | a0001c0001t0002g0003a0001c0001t0002g0071a0001c0001t0002g0161others(163): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.908+2164T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485311 | ||||||
| chr7:76485450
|
G | T | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.908+2303G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485450 | ||||||
| chr7:76485462
|
G | T | 140 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(137): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.908+2315G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485462 | ||||||
| chr7:76485555
|
A | T | 141 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.908+2408A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485555 | ||||||
| chr7:76485565
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0089others(2): Show | 5 | NA18959.hp1 NA18961.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.908+2418C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485565 | ||||||
| chr7:76485612
|
T | G | 1 | a0001c0001t0002g0180 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.908+2465T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485612 | ||||||
| chr7:76485625
|
A | C | 1 | a0004c0006t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.908+2478A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485625 | ||||||
| chr7:76485772
|
A | C | 1 | a0007c0012t0001g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.908+2625A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485772 | ||||||
| chr7:76485816
|
G | A | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+2669G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485816 | ||||||
| chr7:76485920
|
G | A | 1 | a0002c0002t0001g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.908+2773G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485920 | ||||||
| chr7:76486163
|
C | T | 134 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(131): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.908+3016C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486163 | ||||||
| chr7:76486197
|
C | T | 1 | a0001c0001t0002g0179 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.908+3050C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486197 | ||||||
| chr7:76486232
|
C | T | 139 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(136): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.908+3085C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486232 | ||||||
| chr7:76486452
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.908+3305C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486452 | ||||||
| chr7:76486516
|
G | A | 1 | a0002c0011t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.908+3369G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486516 | ||||||
| chr7:76486518
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0002g0097 | 2 | HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.908+3371C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486518 | ||||||
| chr7:76486557
|
G | C | 1 | a0001c0001t0002g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.908+3410G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486557 | ||||||
| chr7:76486558
|
G | A | 1 | a0001c0018t0011g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.908+3411G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486558 | ||||||
| chr7:76486559
|
G | A | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908+3412G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486559 | ||||||
| chr7:76486658
|
A | G | 2 | a0001c0001t0002g0071a0002c0017t0001g0188 | 2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.908+3511A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486658 | ||||||
| chr7:76486688
|
T | C | 3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.908+3541T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486688 | ||||||
| chr7:76486700
|
G | C | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.908+3553G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486700 | ||||||
| chr7:76486712
|
C | T | 1 | a0001c0001t0002g0058 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.908+3565C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486712 | ||||||
| chr7:76486733
|
A | G | 1 | a0004c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.908+3586A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486733 | ||||||
| chr7:76486754
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.908+3607G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486754 | ||||||
| chr7:76486805
|
G | A | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.908+3658G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486805 | ||||||
| chr7:76486810
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.908+3663A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486810 | ||||||
| chr7:76486814
|
C | A | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.908+3667C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486814 | ||||||
| chr7:76486846
|
G | GGCGGCGG others(8): Show |
1 | a0002c0011t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.908+3701_908+3702i others(17): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | |||||
| chr7:76486846
|
G | GGCGGCGG others(14): Show |
1 | a0010c0030t0003g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.908+3701_908+3702i others(23): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | |||||
| chr7:76486846
|
G | GGCGGCGG others(17): Show |
1 | a0002c0011t0003g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.908+3701_908+3702i others(26): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | |||||
| chr7:76486846
|
G | GGCGGCGG others(20): Show |
2 | a0004c0006t0001g0117a0004c0006t0001g0118 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.908+3701_908+3702i others(29): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | |||||
| chr7:76486846
|
G | GGCGGCGG others(23): Show |
7 | a0004c0006t0001g0119a0004c0006t0001g0120a0004c0006t0001g0121others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+3701_908+3702i others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | |||||
| chr7:76486846
|
G | GGCT | 4 | a0001c0001t0001g0088a0001c0001t0002g0054a0001c0001t0002g0097others(1): Show | 4 | HG00609.hp1 HG01258.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+3738_908+3740d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | |||||
| chr7:76486846
|
GGCTGCT | G | 49 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.908+3735_908+3740d others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | |||||
| chr7:76486846
|
GGCTGCTG others(23): Show |
G | 1 | a0002c0002t0001g0197 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.908+3711_908+3740d others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | |||||
| chr7:76486849
|
T | G | 93 | a0001c0001t0002g0071a0001c0003t0001g0116a0001c0003t0001g0128others(90): Show | 93 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.908+3702T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486849 | ||||||
| chr7:76486858
|
T | G | 1 | a0004c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.908+3711T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486858 | ||||||
| chr7:76486861
|
T | G | 1 | a0004c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.908+3714T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486861 | ||||||
| chr7:76486883
|
G | T | 1 | a0004c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.908+3736G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486883 | ||||||
| chr7:76486884
|
C | CTGCTGCT others(44): Show |
1 | a0003c0005t0001g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.908+3740_908+3741i others(53): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(41): Show |
1 | a0003c0005t0001g0015 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.908+3740_908+3741i others(50): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(35): Show |
1 | a0011c0019t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.908+3740_908+3741i others(44): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(32): Show |
3 | a0003c0005t0001g0019a0003c0005t0001g0021a0003c0005t0001g0025 | 3 | HG03239.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.908+3740_908+3741i others(41): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(29): Show |
2 | a0003c0004t0001g0248a0003c0005t0001g0026 | 2 | HG02258.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.908+3740_908+3741i others(38): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(26): Show |
4 | a0003c0004t0001g0238a0003c0004t0001g0246a0003c0004t0001g0249others(1): Show | 4 | HG00639.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(35): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(23): Show |
12 | a0003c0004t0001g0236a0003c0004t0001g0239a0003c0004t0001g0240others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(20): Show |
10 | a0002c0002t0001g0207a0003c0004t0001g0189a0003c0004t0001g0234others(7): Show | 10 | HG00735.hp1 HG01109.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(29): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(17): Show |
2 | a0003c0004t0001g0241a0003c0004t0001g0255 | 2 | HG01081.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.908+3740_908+3741i others(26): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(14): Show |
2 | a0003c0005t0001g0013a0003c0005t0001g0014 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.908+3740_908+3741i others(23): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(8): Show |
4 | a0001c0001t0002g0071a0001c0003t0001g0138a0003c0005t0001g0022others(1): Show | 4 | HG02109.hp1 HG02738.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(17): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(5): Show |
11 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0001g0140others(8): Show | 11 | HG01243.hp2 HG02056.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTGCT others(2): Show |
14 | a0001c0003t0001g0158a0001c0003t0001g0266a0001c0003t0001g0267others(11): Show | 14 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(11): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTGCTTT | 5 | a0001c0003t0001g0146a0001c0003t0001g0154a0002c0020t0009g0011others(2): Show | 5 | HG01891.hp1 HG02647.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | CTTT | 33 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(30): Show | 33 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.908+3738_908+3739i others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | |||||
| chr7:76486884
|
C | T | 1 | a0004c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.908+3737C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486884 | ||||||
| chr7:76486894
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.908+3747C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486894 | ||||||
| chr7:76487119
|
G | A | 3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.908+3972G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487119 | ||||||
| chr7:76487189
|
C | G | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908+4042C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487189 | ||||||
| chr7:76487213
|
G | A | 2 | a0001c0001t0002g0161a0001c0001t0002g0177 | 2 | HG00733.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.908+4066G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487213 | ||||||
| chr7:76487234
|
T | A | 3 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200 | 3 | HG02165.hp2 NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.908+4087T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487234 | ||||||
| chr7:76487258
|
A | G | 1 | a0002c0011t0003g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.908+4111A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487258 | ||||||
| chr7:76487438
|
C | T | 2 | a0001c0003t0001g0145a0001c0003t0001g0151 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.908+4291C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487438 | ||||||
| chr7:76487443
|
G | A | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.908+4296G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487443 | ||||||
| chr7:76487571
|
C | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.908+4424C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487571 | ||||||
| chr7:76487607
|
G | T | 1 | a0002c0002t0001g0186 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.908+4460G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487607 | ||||||
| chr7:76487718
|
C | T | 28 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.909-4435C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487718 | ||||||
| chr7:76487740
|
G | A | 8 | a0004c0006t0001g0115a0004c0006t0001g0119a0004c0006t0001g0120others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-4413G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487740 | ||||||
| chr7:76487757
|
C | T | 18 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054others(15): Show | 18 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.909-4396C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487757 | ||||||
| chr7:76487921
|
G | A | 54 | a0001c0003t0001g0146a0001c0003t0001g0154a0001c0003t0001g0158others(51): Show | 55 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.909-4232G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487921 | ||||||
| chr7:76487930
|
G | A | 6 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0041others(3): Show | 7 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(4): Show |
intron_variant | MODIFIER | c.909-4223G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487930 | ||||||
| chr7:76487960
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-4193C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487960 | ||||||
| chr7:76487975
|
C | T | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-4178C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487975 | ||||||
| chr7:76488056
|
T | C | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-4097T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488056 | ||||||
| chr7:76488125
|
A | T | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-4028A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488125 | ||||||
| chr7:76488153
|
C | T | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-4000C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488153 | ||||||
| chr7:76488171
|
T | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-3982T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488171 | ||||||
| chr7:76488176
|
G | A | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-3977G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488176 | ||||||
| chr7:76488186
|
C | T | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-3967C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488186 | ||||||
| chr7:76488198
|
G | T | 1 | a0002c0002t0001g0208 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.909-3955G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488198 | ||||||
| chr7:76488283
|
G | A | 52 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-3870G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488283 | ||||||
| chr7:76488410
|
G | GC | 275 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(272): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.909-3740dupC | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76488410 | |||||
| chr7:76488427
|
T | C | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.909-3726T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488427 | ||||||
| chr7:76488434
|
T | C | 157 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(154): Show | 158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.909-3719T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488434 | ||||||
| chr7:76488501
|
C | T | 52 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-3652C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488501 | ||||||
| chr7:76488550
|
T | C | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-3603T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488550 | ||||||
| chr7:76488559
|
A | T | 34 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(31): Show | 34 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.909-3594A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488559 | ||||||
| chr7:76488661
|
C | T | 1 | a0002c0002t0001g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.909-3492C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488661 | ||||||
| chr7:76488662
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.909-3491G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488662 | ||||||
| chr7:76488741
|
T | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-3412T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488741 | ||||||
| chr7:76488756
|
C | T | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.909-3397C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488756 | ||||||
| chr7:76488760
|
G | A | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.909-3393G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488760 | ||||||
| chr7:76488782
|
G | C | 1 | a0002c0002t0001g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.909-3371G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488782 | ||||||
| chr7:76488789
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-3364A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488789 | ||||||
| chr7:76488820
|
C | T | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-3333C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488820 | ||||||
| chr7:76488893
|
G | A | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.909-3260G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488893 | ||||||
| chr7:76488894
|
A | AG | 52 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-3258dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76488894 | |||||
| chr7:76488895
|
GA | G | 8 | a0001c0001t0002g0078a0001c0003t0001g0146a0002c0011t0003g0264others(5): Show | 8 | HG02056.hp1 HG02523.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-3245delA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76488895 | |||||
| chr7:76488913
|
G | A | 1 | a0001c0013t0001g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.909-3240G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488913 | ||||||
| chr7:76488950
|
A | T | 105 | a0001c0001t0002g0104a0001c0003t0001g0116a0001c0003t0001g0128others(102): Show | 105 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.909-3203A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488950 | ||||||
| chr7:76489026
|
T | A | 91 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(88): Show | 91 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.909-3127T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489026 | ||||||
| chr7:76489157
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.909-2996A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489157 | ||||||
| chr7:76489251
|
C | T | 1 | a0004c0006t0001g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.909-2902C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489251 | ||||||
| chr7:76489288
|
C | A | 40 | a0002c0008t0001g0229a0002c0008t0001g0230a0003c0004t0001g0189others(37): Show | 40 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.909-2865C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489288 | ||||||
| chr7:76489290
|
A | C | 6 | a0001c0003t0001g0146a0001c0003t0001g0154a0001c0003t0001g0158others(3): Show | 6 | HG00639.hp1 HG00733.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.909-2863A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489290 | ||||||
| chr7:76489469
|
A | G | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-2684A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489469 | ||||||
| chr7:76489518
|
G | A | 52 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-2635G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489518 | ||||||
| chr7:76489553
|
G | C | 33 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(30): Show | 33 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.909-2600G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489553 | ||||||
| chr7:76489624
|
C | T | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-2529C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489624 | ||||||
| chr7:76489640
|
G | T | 103 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(100): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-2513G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489640 | ||||||
| chr7:76489667
|
A | T | 76 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.909-2486A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489667 | ||||||
| chr7:76489875
|
A | C | 52 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-2278A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489875 | ||||||
| chr7:76489896
|
A | C | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-2257A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489896 | ||||||
| chr7:76489899
|
A | AC | 4 | a0001c0001t0002g0093a0001c0001t0002g0103a0002c0002t0001g0190others(1): Show | 4 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-2254_909-2253i others(3): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489899 | ||||||
| chr7:76489899
|
A | C | 52 | a0001c0001t0002g0051a0001c0001t0002g0058a0001c0013t0001g0224others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-2254A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489899 | ||||||
| chr7:76489902
|
C | T | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.909-2251C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489902 | ||||||
| chr7:76490056
|
G | C | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.909-2097G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490056 | ||||||
| chr7:76490068
|
C | A | 2 | a0002c0002t0001g0126a0002c0002t0001g0127 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.909-2085C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490068 | ||||||
| chr7:76490109
|
C | T | 71 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(68): Show | 71 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.909-2044C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490109 | ||||||
| chr7:76490115
|
C | T | 1 | a0001c0003t0001g0148 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.909-2038C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490115 | ||||||
| chr7:76490142
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-2011A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490142 | ||||||
| chr7:76490182
|
T | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-1971T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490182 | ||||||
| chr7:76490257
|
T | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-1896T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490257 | ||||||
| chr7:76490334
|
C | G | 52 | a0001c0013t0001g0224a0001c0023t0006g0023a0002c0002t0001g0004others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-1819C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490334 | ||||||
| chr7:76490334
|
C | T | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-1819C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490334 | ||||||
| chr7:76490385
|
T | C | 104 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(101): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-1768T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490385 | ||||||
| chr7:76490408
|
A | G | 3 | a0001c0001t0002g0106a0001c0001t0002g0108a0002c0002t0001g0004 | 4 | HG01256.hp2 HG01258.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-1745A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490408 | ||||||
| chr7:76490620
|
A | G | 53 | a0001c0001t0002g0105a0001c0013t0001g0224a0002c0002t0001g0004others(50): Show | 54 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.909-1533A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490620 | ||||||
| chr7:76490810
|
C | T | 4 | a0003c0004t0001g0238a0003c0004t0001g0239a0003c0004t0001g0248others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-1343C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490810 | ||||||
| chr7:76490884
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0095 | 3 | NA18961.hp1 NA18967.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.909-1269G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490884 | ||||||
| chr7:76490995
|
C | CTTT | 9 | a0002c0002t0001g0126a0002c0002t0001g0186a0002c0002t0001g0202others(6): Show | 9 | HG00558.hp1 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.909-1141_909-1139d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76490995 | |||||
| chr7:76490995
|
C | CTTTT | 85 | a0001c0013t0001g0224a0001c0031t0001g0273a0002c0002t0001g0004others(82): Show | 86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.909-1142_909-1139d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76490995 | |||||
| chr7:76490995
|
C | CTTTTT | 48 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(45): Show | 48 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.909-1143_909-1139d others(7): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76490995 | |||||
| chr7:76490995
|
C | CTTTTTT | 11 | a0001c0003t0001g0136a0001c0003t0001g0147a0001c0003t0001g0151others(8): Show | 11 | HG01109.hp1 HG01175.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.909-1144_909-1139d others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76490995 | |||||
| chr7:76491053
|
G | A | 33 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(30): Show | 33 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.909-1100G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491053 | ||||||
| chr7:76491060
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.909-1093A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491060 | ||||||
| chr7:76491187
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-966A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491187 | ||||||
| chr7:76491188
|
G | A | 5 | a0003c0005t0001g0013a0003c0005t0001g0014a0003c0005t0001g0018others(2): Show | 5 | HG02818.hp2 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.909-965G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491188 | ||||||
| chr7:76491296
|
A | AT | 9 | a0001c0001t0002g0029a0001c0001t0002g0049a0001c0001t0002g0059others(6): Show | 9 | HG00733.hp2 HG01106.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.909-841dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491296 | |||||
| chr7:76491296
|
AT | A | 67 | a0001c0003t0001g0219a0001c0003t0001g0267a0001c0013t0001g0224others(64): Show | 68 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.909-841delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491296 | |||||
| chr7:76491317
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0173 | 2 | HG02040.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.909-836C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491317 | ||||||
| chr7:76491411
|
A | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-742A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491411 | ||||||
| chr7:76491535
|
G | A | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-618G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491535 | ||||||
| chr7:76491615
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-538A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491615 | ||||||
| chr7:76491624
|
C | CT | 56 | a0001c0013t0001g0224a0002c0002t0001g0004a0002c0002t0001g0125others(53): Show | 57 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.909-520dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491624 | |||||
| chr7:76491686
|
TTA | T | 6 | a0001c0003t0001g0266a0002c0002t0001g0192a0002c0002t0001g0198others(3): Show | 6 | HG00639.hp2 HG02523.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.909-465_909-464del others(2): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491686 | |||||
| chr7:76491687
|
TA | T | 133 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(130): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.909-465delA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491687 | ||||||
| chr7:76491688
|
A | T | 17 | a0001c0003t0001g0146a0002c0002t0001g0211a0002c0002t0007g0201others(14): Show | 17 | HG01109.hp1 HG01175.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.909-465A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491688 | ||||||
| chr7:76491715
|
ACT | A | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.909-435_909-434del others(2): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491715 | |||||
| chr7:76491837
|
C | A | 1 | a0001c0001t0002g0167 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.909-316C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491837 | ||||||
| chr7:76491896
|
AACTCCTG others(41): Show |
A | 1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.909-256_909-209del others(48): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491896 | ||||||
| chr7:76492052
|
A | G | 157 | a0001c0001t0002g0171a0001c0003t0001g0116a0001c0003t0001g0128others(154): Show | 158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.909-101A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76492052 | ||||||
| chr7:76492101
|
C | G | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-52C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76492101 | ||||||
| chr7:76492102
|
G | A | 1 | a0005c0009t0002g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.909-51G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76492102 | ||||||
| chr7:76492265
|
A | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1009+12A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492265 | ||||||
| chr7:76492269
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1009+16C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492269 | ||||||
| chr7:76492295
|
C | CG | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1009+44dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76492295 | |||||
| chr7:76492361
|
A | G | 34 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(31): Show | 34 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1009+108A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492361 | ||||||
| chr7:76492403
|
G | A | 121 | a0001c0013t0001g0224a0001c0031t0001g0273a0002c0002t0001g0004others(118): Show | 122 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1009+150G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492403 | ||||||
| chr7:76492422
|
A | G | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1009+169A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492422 | ||||||
| chr7:76492450
|
C | T | 43 | a0001c0031t0001g0273a0002c0029t0001g0005a0003c0004t0001g0189others(40): Show | 43 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1009+197C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492450 | ||||||
| chr7:76492463
|
A | ACGGTGGG others(4): Show |
11 | a0002c0007t0001g0185a0002c0007t0001g0259a0002c0007t0001g0260others(8): Show | 11 | HG00558.hp2 HG00609.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009+214_1009+224d others(13): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76492463 | |||||
| chr7:76492502
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1009+249A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492502 | ||||||
| chr7:76492939
|
C | T | 1 | a0002c0002t0001g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1009+686C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492939 | ||||||
| chr7:76492940
|
T | C | 1 | a0002c0002t0001g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1009+687T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492940 | ||||||
| chr7:76493121
|
CGCCATGT others(8): Show |
C | 1 | a0002c0002t0001g0202 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1009+869_1009+883d others(17): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493121 | ||||||
| chr7:76493122
|
G | C | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1009+869G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493122 | ||||||
| chr7:76493170
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1009+917C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493170 | ||||||
| chr7:76493203
|
G | A | 145 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(142): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1009+950G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493203 | ||||||
| chr7:76493218
|
C | T | 1 | a0002c0002t0001g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1009+965C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493218 | ||||||
| chr7:76493222
|
G | C | 1 | a0004c0006t0001g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1009+969G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493222 | ||||||
| chr7:76493224
|
C | A | 1 | a0004c0006t0001g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1009+971C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493224 | ||||||
| chr7:76493225
|
A | T | 1 | a0004c0006t0001g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1009+972A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493225 | ||||||
| chr7:76493247
|
A | T | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1009+994A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493247 | ||||||
| chr7:76493321
|
G | A | 144 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(141): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1009+1068G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493321 | ||||||
| chr7:76493322
|
G | A | 1 | a0005c0026t0001g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1009+1069G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493322 | ||||||
| chr7:76493608
|
G | A | 1 | a0004c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1009+1355G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493608 | ||||||
| chr7:76493649
|
A | G | 145 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(142): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1009+1396A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493649 | ||||||
| chr7:76493756
|
G | T | 8 | a0002c0002t0001g0186a0002c0002t0001g0196a0002c0002t0001g0197others(5): Show | 8 | HG01099.hp2 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009+1503G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493756 | ||||||
| chr7:76493860
|
C | G | 155 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(152): Show | 156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1009+1607C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493860 | ||||||
| chr7:76493948
|
T | C | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1009+1695T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493948 | ||||||
| chr7:76493969
|
A | AGAATTTA others(7): Show |
1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1009+1717_1009+173 others(18): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76493969 | |||||
| chr7:76494005
|
T | G | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1009+1752T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494005 | ||||||
| chr7:76494074
|
G | T | 12 | a0002c0007t0001g0185a0002c0007t0001g0259a0002c0007t0001g0260others(9): Show | 12 | HG00558.hp2 HG00609.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1009+1821G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494074 | ||||||
| chr7:76494142
|
AGAGCAGT others(4): Show |
A | 1 | a0002c0002t0001g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1009+1891_1009+190 others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76494142 | |||||
| chr7:76494146
|
C | T | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1009+1893C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494146 | ||||||
| chr7:76494213
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1009+1960A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494213 | ||||||
| chr7:76494276
|
T | C | 2 | a0002c0002t0005g0006a0002c0002t0005g0274 | 2 | HG00735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1009+2023T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494276 | ||||||
| chr7:76494327
|
C | T | 146 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(143): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1009+2074C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494327 | ||||||
| chr7:76494537
|
A | G | 157 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(154): Show | 158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1009+2284A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494537 | ||||||
| chr7:76494579
|
C | T | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1009+2326C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494579 | ||||||
| chr7:76494762
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1009+2509A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494762 | ||||||
| chr7:76494885
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1010-2452C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494885 | ||||||
| chr7:76494930
|
G | A | 1 | a0002c0008t0001g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1010-2407G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494930 | ||||||
| chr7:76494941
|
C | T | 146 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(143): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1010-2396C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494941 | ||||||
| chr7:76494955
|
C | A | 1 | a0002c0007t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1010-2382C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494955 | ||||||
| chr7:76494959
|
C | G | 275 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(272): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1010-2378C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494959 | ||||||
| chr7:76495246
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1010-2091G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495246 | ||||||
| chr7:76495368
|
T | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-1969T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495368 | ||||||
| chr7:76495665
|
G | T | 1 | a0003c0004t0001g0244 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1010-1672G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495665 | ||||||
| chr7:76495678
|
G | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1010-1659G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495678 | ||||||
| chr7:76495798
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1010-1539A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495798 | ||||||
| chr7:76495842
|
T | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-1495T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495842 | ||||||
| chr7:76495847
|
C | G | 1 | a0001c0001t0002g0105 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1010-1490C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495847 | ||||||
| chr7:76495906
|
G | A | 1 | a0003c0005t0001g0025 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1010-1431G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495906 | ||||||
| chr7:76495931
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-1406A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495931 | ||||||
| chr7:76495959
|
T | C | 154 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(151): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1010-1378T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495959 | ||||||
| chr7:76495959
|
T | G | 2 | a0002c0002t0001g0126a0002c0002t0001g0127 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1010-1378T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495959 | ||||||
| chr7:76495963
|
C | T | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-1374C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495963 | ||||||
| chr7:76495969
|
T | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-1368T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495969 | ||||||
| chr7:76495983
|
C | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-1354C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495983 | ||||||
| chr7:76496011
|
C | T | 152 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(149): Show | 153 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1010-1326C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496011 | ||||||
| chr7:76496048
|
G | A | 1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1010-1289G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496048 | ||||||
| chr7:76496112
|
G | C | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-1225G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496112 | ||||||
| chr7:76496113
|
C | G | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-1224C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496113 | ||||||
| chr7:76496114
|
T | C | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-1223T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496114 | ||||||
| chr7:76496132
|
G | GC | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-1205_1010-120 others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496132 | ||||||
| chr7:76496160
|
C | T | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-1177C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496160 | ||||||
| chr7:76496221
|
G | A | 2 | a0002c0011t0003g0264a0010c0030t0003g0263 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1010-1116G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496221 | ||||||
| chr7:76496293
|
C | T | 1 | a0003c0005t0001g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1010-1044C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496293 | ||||||
| chr7:76496339
|
T | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-998T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496339 | ||||||
| chr7:76496415
|
A | C | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-922A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496415 | ||||||
| chr7:76496415
|
A | G | 155 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(152): Show | 156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-922A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496415 | ||||||
| chr7:76496433
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1010-904A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496433 | ||||||
| chr7:76496485
|
C | T | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1010-852C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496485 | ||||||
| chr7:76496498
|
G | GGAGCTGG others(6): Show |
1 | a0001c0001t0002g0037 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1010-837_1010-825d others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76496498 | |||||
| chr7:76496530
|
A | AG | 3 | a0001c0003t0001g0147a0001c0003t0001g0158a0002c0002t0001g0196 | 3 | HG01099.hp2 HG01175.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1010-804dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76496530 | |||||
| chr7:76496565
|
C | A | 1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1010-772C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496565 | ||||||
| chr7:76496565
|
C | T | 150 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(147): Show | 151 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1010-772C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496565 | ||||||
| chr7:76496664
|
G | A | 43 | a0001c0031t0001g0273a0003c0004t0001g0189a0003c0004t0001g0234others(40): Show | 43 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1010-673G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496664 | ||||||
| chr7:76496692
|
C | T | 1 | a0002c0002t0001g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1010-645C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496692 | ||||||
| chr7:76496743
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1010-594G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496743 | ||||||
| chr7:76496802
|
A | T | 1 | a0002c0002t0001g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1010-535A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496802 | ||||||
| chr7:76496825
|
C | T | 3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1010-512C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496825 | ||||||
| chr7:76496909
|
A | C | 1 | a0005c0026t0001g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1010-428A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496909 | ||||||
| chr7:76496909
|
A | G | 154 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(151): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1010-428A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496909 | ||||||
| chr7:76496910
|
C | G | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-427C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496910 | ||||||
| chr7:76496981
|
T | A | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-356T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496981 | ||||||
| chr7:76496982
|
G | T | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-355G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496982 | ||||||
| chr7:76496984
|
A | G | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-353A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496984 | ||||||
| chr7:76497042
|
G | A | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1010-295G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76497042 | ||||||
| chr7:76497184
|
C | T | 2 | a0001c0001t0002g0092a0001c0001t0002g0102 | 2 | HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1010-153C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76497184 | ||||||
| chr7:76497260
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1010-77G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76497260 | ||||||
| chr7:76497284
|
G | T | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1010-53G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76497284 | ||||||
| chr7:76497524
|
C | T | 121 | a0001c0013t0001g0224a0001c0031t0001g0273a0002c0002t0001g0004others(118): Show | 122 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1150+47C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497524 | ||||||
| chr7:76497540
|
T | C | 164 | a0001c0001t0002g0003a0001c0001t0002g0167a0001c0001t0002g0171others(161): Show | 166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1150+63T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497540 | ||||||
| chr7:76497583
|
C | T | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1150+106C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497583 | ||||||
| chr7:76497612
|
C | A | 1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150+135C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497612 | ||||||
| chr7:76497642
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1150+165C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497642 | ||||||
| chr7:76497664
|
C | T | 1 | a0002c0002t0001g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1150+187C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497664 | ||||||
| chr7:76497707
|
A | G | 1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1150+230A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497707 | ||||||
| chr7:76497750
|
A | G | 2 | a0001c0003t0001g0157a0002c0008t0001g0229 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1150+273A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497750 | ||||||
| chr7:76497754
|
G | T | 154 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(151): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1150+277G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497754 | ||||||
| chr7:76497755
|
T | A | 1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150+278T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497755 | ||||||
| chr7:76497788
|
C | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1150+311C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497788 | ||||||
| chr7:76497837
|
C | T | 12 | a0002c0007t0001g0185a0002c0007t0001g0259a0002c0007t0001g0260others(9): Show | 12 | HG00558.hp2 HG00609.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+360C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497837 | ||||||
| chr7:76497849
|
GGCCCAGG others(6): Show |
G | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150+390_1150+402d others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76497849 | |||||
| chr7:76497932
|
G | A | 1 | a0003c0004t0001g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1150+455G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497932 | ||||||
| chr7:76498056
|
C | A | 1 | a0001c0003t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1150+579C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498056 | ||||||
| chr7:76498058
|
A | G | 1 | a0001c0003t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1150+581A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498058 | ||||||
| chr7:76498060
|
C | T | 38 | a0001c0031t0001g0273a0003c0004t0001g0189a0003c0004t0001g0234others(35): Show | 38 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1150+583C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498060 | ||||||
| chr7:76498072
|
C | T | 141 | a0001c0001t0002g0110a0001c0001t0002g0166a0001c0003t0001g0116others(138): Show | 142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1150+595C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498072 | ||||||
| chr7:76498120
|
C | T | 5 | a0001c0001t0002g0040a0002c0002t0001g0193a0002c0002t0001g0209others(2): Show | 5 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150+643C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498120 | ||||||
| chr7:76498136
|
T | TG | 3 | a0001c0001t0002g0061a0002c0002t0001g0187a0002c0002t0001g0226 | 3 | HG00673.hp2 HG04184.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1150+661dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498136 | |||||
| chr7:76498142
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150+665C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498142 | ||||||
| chr7:76498191
|
T | C | 23 | a0001c0001t0002g0089a0001c0003t0001g0128a0001c0003t0001g0129others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1150+714T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498191 | ||||||
| chr7:76498236
|
C | T | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1150+759C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498236 | ||||||
| chr7:76498260
|
G | A | 1 | a0014c0016t0001g0227 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1150+783G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498260 | ||||||
| chr7:76498270
|
C | T | 2 | a0001c0003t0001g0220a0001c0023t0006g0023 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1150+793C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498270 | ||||||
| chr7:76498291
|
G | A | 1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150+814G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498291 | ||||||
| chr7:76498337
|
G | A | 1 | a0001c0003t0001g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1150+860G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498337 | ||||||
| chr7:76498366
|
G | A | 1 | a0001c0001t0002g0079 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1150+889G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498366 | ||||||
| chr7:76498389
|
C | A | 1 | a0001c0001t0002g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1150+912C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498389 | ||||||
| chr7:76498537
|
C | T | 160 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0109others(157): Show | 161 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1150+1060C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498537 | ||||||
| chr7:76498569
|
G | C | 1 | a0002c0008t0004g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1150+1092G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498569 | ||||||
| chr7:76498570
|
C | CG | 7 | a0001c0001t0002g0036a0001c0001t0002g0052a0001c0001t0002g0181others(4): Show | 7 | HG00673.hp2 HG02056.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+1098dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498570 | |||||
| chr7:76498570
|
C | G | 1 | a0002c0008t0004g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1150+1093C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498570 | ||||||
| chr7:76498616
|
G | A | 29 | a0001c0031t0001g0273a0003c0004t0001g0189a0003c0004t0001g0234others(26): Show | 29 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1150+1139G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498616 | ||||||
| chr7:76498625
|
G | A | 1 | a0002c0002t0001g0221 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1150+1148G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498625 | ||||||
| chr7:76498716
|
C | T | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1150+1239C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498716 | ||||||
| chr7:76498727
|
TG | T | 155 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(152): Show | 156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1150+1255delG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498727 | |||||
| chr7:76498738
|
G | A | 1 | a0003c0005t0001g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1150+1261G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498738 | ||||||
| chr7:76498768
|
A | C | 43 | a0001c0031t0001g0273a0003c0004t0001g0189a0003c0004t0001g0234others(40): Show | 43 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1150+1291A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498768 | ||||||
| chr7:76498788
|
C | CTGGGATG others(17): Show |
1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150+1313_1150+131 others(28): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498788 | |||||
| chr7:76498788
|
CTGTA | C | 124 | a0001c0003t0001g0116a0001c0003t0001g0136a0001c0003t0001g0137others(121): Show | 125 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1150+1314_1150+131 others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498788 | |||||
| chr7:76498789
|
T | TGGGTGTG others(5): Show |
4 | a0004c0006t0001g0120a0004c0006t0001g0121a0004c0006t0001g0122others(1): Show | 4 | HG01884.hp1 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+1313_1150+131 others(16): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498789 | |||||
| chr7:76498791
|
T | G | 27 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(24): Show | 27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1150+1314T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498791 | ||||||
| chr7:76498792
|
A | G | 28 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(25): Show | 28 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.1150+1315A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498792 | ||||||
| chr7:76498794
|
G | GGGGGTGT others(4): Show |
4 | a0004c0006t0001g0120a0004c0006t0001g0121a0004c0006t0001g0122others(1): Show | 4 | HG01884.hp1 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+1319_1150+132 others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498794 | |||||
| chr7:76498794
|
G | GGGTGTGT others(3): Show |
1 | a0002c0002t0001g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1150+1324_1150+133 others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498794 | |||||
| chr7:76498794
|
G | GGGTGTGT others(21): Show |
2 | a0002c0007t0001g0259a0002c0028t0001g0258 | 2 | HG01496.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1150+1336_1150+133 others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498794 | |||||
| chr7:76498794
|
G | GGGTGTGT others(20): Show |
71 | a0001c0003t0001g0116a0001c0003t0001g0136a0001c0003t0001g0137others(68): Show | 72 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1150+1336_1150+133 others(31): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498794 | |||||
| chr7:76498794
|
G | GTGTGGAG others(16): Show |
27 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(24): Show | 27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1150+1317_1150+131 others(27): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498794 | ||||||
| chr7:76498809
|
T | TGGGGGTG others(21): Show |
2 | a0001c0031t0001g0273a0002c0017t0001g0188 | 2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1150+1336_1150+133 others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498809 | |||||
| chr7:76498810
|
G | GGGGGTGT others(45): Show |
3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1150+1336_1150+133 others(56): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498810 | |||||
| chr7:76498810
|
G | GGGGGTGT others(70): Show |
1 | a0002c0002t0001g0203 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1150+1336_1150+133 others(81): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498810 | |||||
| chr7:76498811
|
GGGTGTGT others(17): Show |
G | 1 | a0001c0001t0002g0093 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1150+1337_1150+136 others(28): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498811 | |||||
| chr7:76498817
|
G | A | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1150+1340G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498817 | ||||||
| chr7:76498820
|
G | A | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1150+1343G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498820 | ||||||
| chr7:76498828
|
A | G | 114 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(111): Show | 115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1150+1351A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498828 | ||||||
| chr7:76498835
|
A | G | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1150+1358A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498835 | ||||||
| chr7:76498845
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1150+1368G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498845 | ||||||
| chr7:76498859
|
G | T | 1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1150+1382G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498859 | ||||||
| chr7:76498860
|
A | G | 1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1150+1383A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498860 | ||||||
| chr7:76498861
|
G | A | 1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1150+1384G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498861 | ||||||
| chr7:76498871
|
G | A | 1 | a0003c0005t0001g0026 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1150+1394G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498871 | ||||||
| chr7:76498871
|
G | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1150+1394G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498871 | ||||||
| chr7:76498889
|
G | C | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1150+1412G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498889 | ||||||
| chr7:76498917
|
GT | G | 155 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(152): Show | 156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1150+1441delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498917 | ||||||
| chr7:76498918
|
T | G | 1 | a0001c0003t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1150+1441T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498918 | ||||||
| chr7:76498919
|
G | T | 1 | a0001c0003t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1150+1442G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498919 | ||||||
| chr7:76498969
|
G | T | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1151-1472G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498969 | ||||||
| chr7:76499011
|
A | AGT | 144 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(141): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1151-1426_1151-142 others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499011 | |||||
| chr7:76499017
|
G | T | 9 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1151-1424G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499017 | ||||||
| chr7:76499020
|
T | G | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1151-1421T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499020 | ||||||
| chr7:76499026
|
A | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1151-1415A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499026 | ||||||
| chr7:76499030
|
G | A | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1151-1411G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499030 | ||||||
| chr7:76499041
|
T | A | 1 | a0002c0007t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1151-1400T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499041 | ||||||
| chr7:76499055
|
T | G | 1 | a0002c0002t0001g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1151-1386T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499055 | ||||||
| chr7:76499097
|
G | T | 1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1151-1344G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499097 | ||||||
| chr7:76499117
|
C | G | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1151-1324C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499117 | ||||||
| chr7:76499154
|
T | TGGGTGTG others(2948): Show |
1 | a0002c0002t0005g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1151-1286_1151-128 others(2959): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3039): Show |
1 | a0001c0001t0002g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(3050): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3044): Show |
1 | a0004c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(3055): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2970): Show |
1 | a0001c0003t0001g0147 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(2981): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2942): Show |
1 | a0003c0004t0001g0242 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2931): Show |
1 | a0003c0004t0001g0249 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(2942): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3033): Show |
1 | a0001c0001t0002g0047 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3044): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3032): Show |
1 | a0001c0001t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3030): Show |
1 | a0001c0001t0002g0030 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3041): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3034): Show |
1 | a0005c0009t0002g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3112): Show |
1 | a0001c0001t0002g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3123): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3106): Show |
1 | a0001c0001t0002g0102 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3117): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3034): Show |
1 | a0005c0009t0008g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3032): Show |
1 | a0001c0023t0006g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3104): Show |
1 | a0001c0001t0002g0105 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3115): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3024): Show |
1 | a0001c0001t0002g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3035): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3033): Show |
1 | a0001c0001t0002g0032 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3044): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3032): Show |
1 | a0001c0001t0002g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3030): Show |
2 | a0001c0001t0002g0161a0001c0001t0002g0177 | 2 | HG00733.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3041): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3008): Show |
1 | a0001c0001t0002g0059 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3019): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3115): Show |
1 | a0001c0001t0002g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3126): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3108): Show |
1 | a0001c0001t0002g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3119): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3087): Show |
1 | a0001c0001t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3098): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3086): Show |
3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0114 | 3 | HG02451.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3097): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3086): Show |
1 | a0001c0001t0002g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3097): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3083): Show |
1 | a0001c0001t0002g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3094): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3034): Show |
1 | a0001c0001t0002g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3111): Show |
1 | a0001c0001t0002g0009 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3122): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3107): Show |
1 | a0001c0001t0002g0095 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3118): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3109): Show |
1 | a0001c0001t0002g0008 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3120): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3108): Show |
2 | a0001c0001t0002g0012a0001c0001t0002g0090 | 2 | NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3119): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3112): Show |
2 | a0001c0001t0002g0106a0001c0001t0002g0108 | 2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3123): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3108): Show |
1 | a0001c0001t0002g0093 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3119): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3111): Show |
7 | a0001c0001t0001g0088a0001c0001t0002g0096a0001c0001t0002g0097others(4): Show | 7 | HG01071.hp1 HG01106.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3122): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3109): Show |
1 | a0001c0001t0002g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3120): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3110): Show |
1 | a0012c0022t0002g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3121): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3016): Show |
3 | a0001c0001t0002g0068a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | HG02056.hp1 HG02155.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3027): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3035): Show |
1 | a0001c0001t0002g0076 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3046): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3035): Show |
1 | a0001c0001t0002g0063 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3046): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3034): Show |
2 | a0001c0001t0002g0044a0001c0001t0002g0175 | 2 | HG04228.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3035): Show |
1 | a0001c0001t0002g0169 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3046): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3033): Show |
44 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(41): Show | 47 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3044): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3032): Show |
1 | a0001c0001t0002g0049 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3030): Show |
1 | a0001c0001t0002g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3041): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3004): Show |
1 | a0001c0001t0002g0065 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3015): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3032): Show |
2 | a0001c0001t0002g0110a0001c0001t0002g0167 | 2 | HG02970.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3060): Show |
3 | a0006c0010t0002g0010a0006c0010t0002g0087a0006c0010t0002g0098 | 3 | HG03490.hp1 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3071): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3039): Show |
1 | a0001c0001t0002g0178 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3050): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3077): Show |
1 | a0001c0001t0002g0085 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3088): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2830): Show |
1 | a0001c0001t0002g0052 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2841): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2824): Show |
4 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0055others(1): Show | 4 | HG00609.hp1 HG01934.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2835): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3104): Show |
1 | a0001c0001t0002g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3115): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3086): Show |
1 | a0001c0001t0002g0089 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3097): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3044): Show |
1 | a0001c0001t0002g0037 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3055): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3034): Show |
1 | a0005c0009t0002g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3106): Show |
1 | a0001c0001t0002g0082 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3117): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3110): Show |
1 | a0001c0018t0011g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3121): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3034): Show |
1 | a0001c0001t0002g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3033): Show |
3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0072 | 3 | HG02257.hp1 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3044): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3060): Show |
1 | a0002c0007t0001g0259 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3071): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2946): Show |
1 | a0005c0026t0001g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2945): Show |
1 | a0001c0003t0001g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2956): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3022): Show |
1 | a0004c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3033): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2942): Show |
1 | a0001c0003t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2947): Show |
1 | a0001c0003t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2958): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2946): Show |
1 | a0001c0003t0001g0144 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2947): Show |
1 | a0001c0003t0001g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2958): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2947): Show |
1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2958): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2948): Show |
1 | a0001c0003t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2959): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2947): Show |
1 | a0001c0003t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2958): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2946): Show |
1 | a0001c0003t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2946): Show |
6 | a0001c0003t0001g0129a0001c0003t0001g0131a0001c0003t0001g0145others(3): Show | 6 | HG00597.hp2 HG01975.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2946): Show |
3 | a0001c0003t0001g0116a0001c0003t0001g0219a0001c0003t0001g0220 | 3 | HG02723.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2946): Show |
6 | a0001c0003t0001g0136a0001c0003t0001g0138a0001c0003t0001g0140others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2945): Show |
1 | a0001c0003t0001g0130 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2956): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2945): Show |
1 | a0001c0003t0001g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2956): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2946): Show |
1 | a0001c0003t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2949): Show |
1 | a0001c0003t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2960): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2949): Show |
1 | a0001c0003t0001g0267 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2960): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2926): Show |
1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2937): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2893): Show |
3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2904): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2925): Show |
1 | a0005c0033t0001g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2936): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2924): Show |
4 | a0003c0004t0001g0238a0003c0004t0001g0248a0007c0012t0001g0232others(1): Show | 4 | HG00639.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2935): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2905): Show |
1 | a0003c0005t0001g0026 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2916): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2904): Show |
13 | a0003c0005t0001g0013a0003c0005t0001g0014a0003c0005t0001g0015others(10): Show | 13 | HG00639.hp2 HG01192.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2915): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3190): Show |
2 | a0002c0008t0004g0132a0002c0008t0004g0133 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3201): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2943): Show |
1 | a0001c0031t0001g0273 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2954): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2945): Show |
1 | a0002c0007t0001g0275 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2956): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2942): Show |
8 | a0002c0007t0001g0185a0002c0007t0001g0260a0002c0007t0001g0268others(5): Show | 8 | HG00558.hp2 HG00609.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2942): Show |
1 | a0002c0028t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3192): Show |
1 | a0002c0008t0004g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3203): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2938): Show |
1 | a0003c0004t0001g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2949): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2941): Show |
14 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0236others(11): Show | 14 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2952): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2939): Show |
1 | a0003c0004t0001g0237 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2950): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2840): Show |
1 | a0003c0004t0001g0235 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2851): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3021): Show |
1 | a0004c0006t0001g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3032): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3022): Show |
2 | a0004c0006t0001g0120a0004c0006t0001g0122 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3033): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3019): Show |
1 | a0004c0006t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3030): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3022): Show |
2 | a0004c0006t0001g0117a0004c0006t0001g0123 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3033): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3023): Show |
1 | a0004c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3034): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2943): Show |
1 | a0001c0003t0001g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2954): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2940): Show |
1 | a0001c0003t0001g0148 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2951): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2940): Show |
1 | a0001c0003t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2951): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3080): Show |
1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3091): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2958): Show |
1 | a0003c0004t0001g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2969): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(2942): Show |
1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGAGG others(3029): Show |
1 | a0004c0006t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1151-1276_1151-127 others(3040): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2955): Show |
1 | a0002c0002t0001g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2966): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2955): Show |
1 | a0002c0002t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2966): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2952): Show |
1 | a0002c0002t0001g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2963): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2955): Show |
1 | a0002c0002t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2966): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2952): Show |
1 | a0002c0002t0001g0206 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2963): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2952): Show |
1 | a0002c0002t0001g0204 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2963): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0231 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2956): Show |
1 | a0002c0002t0001g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2967): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2953): Show |
1 | a0002c0002t0001g0214 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2964): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2951): Show |
5 | a0002c0002t0001g0186a0002c0002t0001g0197a0002c0002t0001g0202others(2): Show | 5 | HG01928.hp2 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2962): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2951): Show |
17 | a0002c0002t0001g0125a0002c0002t0001g0126a0002c0002t0001g0127others(14): Show | 17 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2962): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2951): Show |
1 | a0001c0013t0001g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2962): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2950): Show |
4 | a0002c0002t0001g0004a0002c0002t0001g0217a0002c0002t0001g0218others(1): Show | 5 | HG01123.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2934): Show |
1 | a0002c0002t0001g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2945): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(3434): Show |
1 | a0009c0015t0001g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(3445): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0221 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2935): Show |
2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2946): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2948): Show |
3 | a0002c0002t0001g0193a0002c0002t0001g0209a0002c0002t0001g0222 | 3 | HG02622.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2959): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499154
|
T | TGTGGGGT others(2988): Show |
1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2999): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | |||||
| chr7:76499158
|
G | GAGGTGTG others(2921): Show |
1 | a0003c0004t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2932): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499158 | |||||
| chr7:76499158
|
G | GAGGTGTG others(2920): Show |
2 | a0003c0004t0001g0241a0003c0004t0001g0250 | 2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2931): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499158 | |||||
| chr7:76499190
|
G | T | 2 | a0003c0004t0001g0237a0003c0004t0001g0247 | 2 | HG03704.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1151-1251G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499190 | ||||||
| chr7:76499231
|
A | G | 1 | a0003c0004t0001g0262 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1151-1210A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499231 | ||||||
| chr7:76499273
|
C | T | 1 | a0002c0028t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1151-1168C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499273 | ||||||
| chr7:76499276
|
G | C | 1 | a0002c0028t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1151-1165G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499276 | ||||||
| chr7:76499277
|
T | G | 2 | a0002c0028t0001g0258a0005c0027t0001g0139 | 2 | HG02056.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1151-1164T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499277 | ||||||
| chr7:76499286
|
A | G | 3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1151-1155A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499286 | ||||||
| chr7:76499349
|
C | T | 3 | a0001c0001t0002g0169a0001c0001t0002g0182a0002c0029t0001g0005 | 3 | HG03225.hp1 NA18967.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1151-1092C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499349 | ||||||
| chr7:76499354
|
C | T | 4 | a0001c0001t0002g0040a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151-1087C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499354 | ||||||
| chr7:76499368
|
A | G | 156 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(153): Show | 157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1151-1073A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499368 | ||||||
| chr7:76499488
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1151-953C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499488 | ||||||
| chr7:76499600
|
C | G | 73 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1151-841C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499600 | ||||||
| chr7:76499663
|
A | G | 3 | a0002c0011t0003g0264a0002c0011t0003g0265a0010c0030t0003g0263 | 3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1151-778A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499663 | ||||||
| chr7:76499693
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1151-748G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499693 | ||||||
| chr7:76499697
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1151-744C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499697 | ||||||
| chr7:76499800
|
A | G | 46 | a0001c0001t0002g0041a0001c0001t0002g0046a0001c0001t0002g0183others(43): Show | 46 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1151-641A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499800 | ||||||
| chr7:76499801
|
C | T | 46 | a0001c0001t0002g0041a0001c0001t0002g0046a0001c0001t0002g0183others(43): Show | 46 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1151-640C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499801 | ||||||
| chr7:76499931
|
G | C | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1151-510G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499931 | ||||||
| chr7:76499985
|
C | G | 49 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(46): Show | 49 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1151-456C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499985 | ||||||
| chr7:76500047
|
G | C | 157 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(154): Show | 158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1151-394G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500047 | ||||||
| chr7:76500080
|
G | A | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1151-361G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500080 | ||||||
| chr7:76500202
|
A | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0109a0001c0001t0002g0110 | 3 | HG02970.hp1 HG03453.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1151-239A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500202 | ||||||
| chr7:76500222
|
G | A | 79 | a0001c0003t0001g0128a0001c0003t0001g0129a0001c0003t0001g0130others(76): Show | 79 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1151-219G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500222 | ||||||
| chr7:76500249
|
G | A | 1 | a0002c0002t0001g0231 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1151-192G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500249 | ||||||
| chr7:76500368
|
C | G | 159 | a0001c0001t0002g0169a0001c0001t0002g0182a0001c0003t0001g0116others(156): Show | 160 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1151-73C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500368 | ||||||
| chr7:76500414
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1151-27C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500414 | ||||||
| chr7:76500546
|
C | T | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+26C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500546 | ||||||
| chr7:76500597
|
T | G | 1 | a0001c0001t0002g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1230+77T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500597 | ||||||
| chr7:76500613
|
T | G | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1230+93T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500613 | ||||||
| chr7:76500642
|
G | C | 43 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0235others(40): Show | 43 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1230+122G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500642 | ||||||
| chr7:76500674
|
C | T | 2 | a0001c0001t0002g0106a0001c0001t0002g0108 | 2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1230+154C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500674 | ||||||
| chr7:76500686
|
A | G | 2 | a0002c0020t0009g0011a0002c0032t0001g0256 | 2 | HG00733.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+166A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500686 | ||||||
| chr7:76500695
|
G | A | 3 | a0001c0001t0002g0169a0001c0001t0002g0182a0002c0020t0009g0011 | 3 | HG02897.hp1 NA18967.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230+175G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500695 | ||||||
| chr7:76500793
|
A | G | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+273A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500793 | ||||||
| chr7:76500839
|
C | T | 1 | a0003c0004t0001g0234 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1230+319C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500839 | ||||||
| chr7:76500933
|
A | T | 1 | a0003c0005t0001g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1230+413A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500933 | ||||||
| chr7:76500971
|
T | A | 43 | a0003c0004t0001g0189a0003c0004t0001g0234a0003c0004t0001g0235others(40): Show | 43 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1230+451T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500971 | ||||||
| chr7:76500993
|
A | C | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1230+473A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500993 | ||||||
| chr7:76501018
|
C | T | 1 | a0003c0005t0001g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1230+498C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501018 | ||||||
| chr7:76501019
|
T | C | 1 | a0003c0005t0001g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1230+499T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501019 | ||||||
| chr7:76501151
|
A | G | 1 | a0002c0002t0001g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1230+631A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501151 | ||||||
| chr7:76501157
|
T | TG | 3 | a0002c0002t0001g0196a0002c0007t0001g0259a0005c0009t0002g0172 | 3 | HG00621.hp2 HG01099.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1230+640dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 76501157 | |||||
| chr7:76501340
|
C | T | 1 | a0002c0002t0001g0214 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1230+820C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501340 | ||||||
| chr7:76501515
|
G | C | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-783G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501515 | ||||||
| chr7:76501529
|
C | G | 3 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200 | 3 | HG02165.hp2 NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1231-769C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501529 | ||||||
| chr7:76501581
|
C | T | 2 | a0002c0011t0003g0264a0010c0030t0003g0263 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1231-717C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501581 | ||||||
| chr7:76501649
|
A | C | 122 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(119): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1231-649A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501649 | ||||||
| chr7:76501661
|
G | A | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-637G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501661 | ||||||
| chr7:76501737
|
G | T | 2 | a0001c0003t0001g0266a0001c0003t0001g0267 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1231-561G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501737 | ||||||
| chr7:76501744
|
C | T | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-554C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501744 | ||||||
| chr7:76501814
|
G | A | 10 | a0004c0006t0001g0115a0004c0006t0001g0117a0004c0006t0001g0118others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-484G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501814 | ||||||
| chr7:76501850
|
C | G | 1 | a0001c0001t0002g0059 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1231-448C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501850 | ||||||
| chr7:76501852
|
C | T | 117 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(114): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1231-446C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501852 | ||||||
| chr7:76501888
|
CT | C | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1231-394delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 76501888 | |||||
| chr7:76501897
|
T | C | 1 | a0002c0011t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1231-401T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501897 | ||||||
| chr7:76501929
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1231-369C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501929 | ||||||
| chr7:76502011
|
C | G | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-287C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76502011 | ||||||
| chr7:76502019
|
T | A | 1 | a0008c0014t0001g0210 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1231-279T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76502019 | ||||||
| chr7:76502136
|
T | C | 199 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(196): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1231-162T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76502136 | ||||||
| chr7:76502200
|
TC | T | 15 | a0003c0005t0001g0013a0003c0005t0001g0014a0003c0005t0001g0015others(12): Show | 15 | HG00639.hp2 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1231-96delC | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 76502200 | |||||
| chr7:76502269
|
G | A | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-29G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76502269 | ||||||
| chr7:76502472
|
C | A | 1 | a0005c0027t0001g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1389+16C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502472 | ||||||
| chr7:76502495
|
C | G | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1389+39C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502495 | ||||||
| chr7:76502526
|
C | T | 3 | a0001c0003t0001g0146a0001c0003t0001g0154a0001c0003t0001g0158 | 3 | HG01175.hp2 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1389+70C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502526 | ||||||
| chr7:76502538
|
G | A | 2 | a0001c0001t0002g0109a0002c0002t0001g0216 | 2 | HG03453.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1389+82G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502538 | ||||||
| chr7:76502592
|
G | A | 2 | a0001c0013t0001g0224a0014c0016t0001g0227 | 2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1389+136G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502592 | ||||||
| chr7:76502657
|
C | G | 36 | a0001c0001t0001g0088a0001c0001t0002g0008a0001c0001t0002g0009others(33): Show | 36 | HG00741.hp2 HG01071.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.1389+201C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502657 | ||||||
| chr7:76502756
|
C | A | 2 | a0002c0008t0001g0229a0002c0008t0001g0230 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1389+300C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502756 | ||||||
| chr7:76502760
|
C | T | 12 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+304C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502760 | ||||||
| chr7:76502816
|
G | A | 1 | a0003c0004t0001g0235 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1389+360G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502816 | ||||||
| chr7:76502952
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1390-474G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502952 | ||||||
| chr7:76502953
|
C | A | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1390-473C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502953 | ||||||
| chr7:76503060
|
G | A | 71 | a0001c0013t0001g0224a0001c0023t0006g0023a0001c0031t0001g0273others(68): Show | 72 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1390-366G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503060 | ||||||
| chr7:76503080
|
A | G | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1390-346A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503080 | ||||||
| chr7:76503094
|
G | A | 1 | a0004c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1390-332G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503094 | ||||||
| chr7:76503156
|
C | A | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1390-270C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503156 | ||||||
| chr7:76503291
|
G | A | 7 | a0003c0005t0001g0015a0003c0005t0001g0016a0003c0005t0001g0017others(4): Show | 7 | HG00639.hp2 HG01192.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1390-135G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503291 | ||||||
| chr7:76503359
|
C | T | 1 | a0004c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1390-67C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503359 | ||||||
| chr7:76503360
|
G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1390-66G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503360 | ||||||
| chr7:76503374
|
T | C | 2 | a0003c0005t0001g0013a0003c0005t0001g0014 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1390-52T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503374 | ||||||
| chr7:76503421
|
G | C | 1 | a0005c0009t0002g0164 | 1 | HG02080.hp2 | splice_region_variant&intron_variant | LOW | c.1390-5G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503421 | ||||||
| chr7:76503645
|
A | G | 169 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(166): Show | 173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1551+58A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503645 | ||||||
| chr7:76503724
|
A | G | 24 | a0001c0001t0001g0088a0001c0001t0002g0092a0001c0001t0002g0093others(21): Show | 24 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1551+137A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503724 | ||||||
| chr7:76503737
|
C | T | 27 | a0001c0001t0001g0088a0001c0001t0002g0092a0001c0001t0002g0093others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.1551+150C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503737 | ||||||
| chr7:76503757
|
C | T | 74 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(71): Show | 74 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1551+170C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503757 | ||||||
| chr7:76503781
|
G | T | 3 | a0001c0023t0006g0023a0002c0011t0003g0264a0010c0030t0003g0263 | 3 | HG02451.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1551+194G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503781 | ||||||
| chr7:76503814
|
T | C | 15 | a0001c0001t0001g0088a0001c0001t0002g0092a0001c0001t0002g0093others(12): Show | 15 | HG00741.hp2 HG01168.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1551+227T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503814 | ||||||
| chr7:76503818
|
G | A | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1551+231G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503818 | ||||||
| chr7:76503923
|
C | T | 9 | a0001c0031t0001g0273a0002c0007t0001g0268a0002c0007t0001g0270others(6): Show | 9 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.1551+336C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503923 | ||||||
| chr7:76503944
|
G | A | 29 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(26): Show | 29 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1551+357G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503944 | ||||||
| chr7:76504036
|
C | T | 61 | a0001c0013t0001g0224a0001c0031t0001g0273a0002c0002t0001g0004others(58): Show | 62 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1552-320C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504036 | ||||||
| chr7:76504040
|
C | T | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1552-316C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504040 | ||||||
| chr7:76504081
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1552-275G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504081 | ||||||
| chr7:76504092
|
G | T | 16 | a0001c0031t0001g0273a0002c0007t0001g0185a0002c0007t0001g0259others(13): Show | 16 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.1552-264G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504092 | ||||||
| chr7:76504110
|
C | CAG | 129 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(126): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1552-246_1552-245i others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504110 | ||||||
| chr7:76504312
|
C | T | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1552-44C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504312 | ||||||
| chr7:76504321
|
G | A | 1 | a0003c0005t0001g0015 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1552-35G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504321 | ||||||
| chr7:76504461
|
C | A | 3 | a0002c0008t0004g0132a0002c0008t0004g0133a0002c0008t0004g0134 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1641+16C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504461 | ||||||
| chr7:76504466
|
G | C | 270 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(267): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1641+21G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504466 | ||||||
| chr7:76504493
|
G | A | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1641+48G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504493 | ||||||
| chr7:76504534
|
G | A | 1 | a0002c0002t0001g0213 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1641+89G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504534 | ||||||
| chr7:76504558
|
C | T | 1 | a0002c0002t0005g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1641+113C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504558 | ||||||
| chr7:76504584
|
A | G | 31 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(28): Show | 31 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1641+139A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504584 | ||||||
| chr7:76504685
|
T | C | 2 | a0004c0006t0001g0117a0004c0006t0001g0118 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1641+240T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504685 | ||||||
| chr7:76504718
|
G | A | 4 | a0001c0023t0006g0023a0002c0011t0003g0264a0002c0011t0003g0265others(1): Show | 4 | HG02451.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1641+273G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504718 | ||||||
| chr7:76504886
|
G | T | 71 | a0001c0013t0001g0224a0001c0023t0006g0023a0001c0031t0001g0273others(68): Show | 72 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1641+441G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504886 | ||||||
| chr7:76504919
|
C | T | 117 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(114): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1642-455C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504919 | ||||||
| chr7:76505081
|
C | T | 32 | a0001c0003t0001g0116a0001c0003t0001g0128a0001c0003t0001g0129others(29): Show | 32 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1642-293C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505081 | ||||||
| chr7:76505116
|
C | A | 118 | a0001c0001t0001g0088a0001c0001t0002g0001a0001c0001t0002g0002others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1642-258C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505116 | ||||||
| chr7:76505167
|
G | C | 4 | a0004c0006t0001g0120a0004c0006t0001g0121a0004c0006t0001g0122others(1): Show | 4 | HG01884.hp1 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1642-207G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505167 | ||||||
| chr7:76505264
|
C | T | 2 | a0002c0007t0001g0275a0002c0007t0001g0276 | 2 | HG00609.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1642-110C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505264 | ||||||
| chr7:76505356
|
C | G | 3 | a0001c0001t0002g0009a0001c0001t0002g0096a0001c0001t0002g0099 | 3 | HG01071.hp1 HG01106.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1642-18C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505356 |