Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9993 |
|---|---|
| ensemblid | ENSG00000070413.21 |
| hgncid | 2845 |
| symbol | DGCR2 |
| name | DiGeorge syndrome critical region gene 2 |
| refseq_nuc | NM_005137.3 |
| refseq_prot | NP_005128.1 |
| ensembl_nuc | ENST00000263196.12 |
| ensembl_prot | ENSP00000263196.7 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 19036286 |
| end | 19122412 |
| strand | - |
| ver | v1.2 |
| region | chr22:19036286-19122412 |
| region5000 | chr22:19031286-19127412 |
| regionname0 | DGCR2_chr22_19036286_19122412 |
| regionname5000 | DGCR2_chr22_19031286_19127412 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 550 | 158 | 37 | 31 | 68 | 5 | 16 | 40 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002 | 0/1 | 550 | 153 | 49 | 29 | 54 | 5 | 15 | 43 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0003 | 0/0 | 550 | 30 | 0 | 8 | 17 | 0 | 5 | 14 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0004 | 0/0 | 550 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0005 | 0/0 | 550 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0006 | 0/0 | 550 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1653 | 151 | 37 | 28 | 68 | 5 | 12 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| c0002 | 0/1 | 1653 | 147 | 44 | 28 | 54 | 5 | 15 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| c0003 | 0/0 | 1653 | 30 | 0 | 8 | 17 | 0 | 5 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| c0004 | 0/0 | 1653 | 7 | 0 | 3 | 0 | 0 | 4 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| c0005 | 0/0 | 1653 | 6 | 5 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| c0006 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| c0007 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| c0008 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2786 | 112 | 10 | 25 | 59 | 5 | 12 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0002 | 0/0 | 2800 | 35 | 1 | 7 | 20 | 1 | 6 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0003 | 0/0 | 2786 | 25 | 6 | 9 | 8 | 0 | 2 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0004 | 0/0 | 2787 | 20 | 1 | 3 | 11 | 0 | 5 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0005 | 0/0 | 2786 | 18 | 10 | 1 | 7 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0006 | 0/0 | 2800 | 11 | 11 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0007 | 0/0 | 2800 | 10 | 0 | 3 | 5 | 0 | 2 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0008 | 0/0 | 2800 | 10 | 0 | 0 | 8 | 0 | 2 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0009 | 0/0 | 2787 | 10 | 7 | 3 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0010 | 0/0 | 2786 | 8 | 8 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0011 | 0/0 | 2786 | 8 | 6 | 2 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0012 | 0/0 | 2800 | 7 | 0 | 5 | 2 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0013 | 0/0 | 2787 | 6 | 0 | 1 | 4 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0014 | 0/0 | 2786 | 4 | 0 | 0 | 4 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0015 | 0/0 | 2786 | 4 | 0 | 1 | 0 | 0 | 3 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0016 | 0/0 | 2786 | 4 | 3 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0017 | 0/0 | 2800 | 4 | 0 | 0 | 4 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0018 | 0/0 | 2800 | 4 | 0 | 2 | 1 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0019 | 0/0 | 2805 | 3 | 3 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0020 | 0/0 | 2800 | 3 | 3 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0021 | 0/0 | 2786 | 3 | 0 | 0 | 3 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0022 | 0/0 | 2786 | 2 | 2 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0023 | 0/0 | 2786 | 2 | 0 | 2 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0024 | 0/0 | 2786 | 2 | 2 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0025 | 0/0 | 2800 | 2 | 0 | 0 | 0 | 2 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0026 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0027 | 0/0 | 2800 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0028 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0029 | 0/0 | 2786 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0030 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0031 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0032 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0033 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0034 | 0/0 | 2786 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0035 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0036 | 0/0 | 2786 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0037 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0038 | 0/0 | 2786 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0039 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0040 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0041 | 0/0 | 2800 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0042 | 0/1 | 2800 | 1 | 0 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0043 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0044 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0045 | 0/0 | 2800 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0046 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0047 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0048 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0049 | 0/0 | 2786 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0050 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0051 | 0/0 | 2786 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| t0052 | 0/0 | 2786 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| 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 | 3 | 3 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1653 | 151 | 37 | 28 | 68 | 5 | 12 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0004 | 0/0 | 1653 | 7 | 0 | 3 | 0 | 0 | 4 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002 | 0/1 | 1653 | 147 | 44 | 28 | 54 | 5 | 15 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0005 | 0/0 | 1653 | 6 | 5 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0003c0003 | 0/0 | 1653 | 30 | 0 | 8 | 17 | 0 | 5 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0004c0008 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0005c0006 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0006c0007 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4438 | 110 | 10 | 25 | 57 | 5 | 12 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0005 | 0/0 | 4438 | 17 | 10 | 1 | 6 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0010 | 0/0 | 4438 | 8 | 8 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0016 | 0/0 | 4438 | 4 | 3 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0021 | 0/0 | 4438 | 3 | 0 | 0 | 3 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0024 | 0/0 | 4438 | 2 | 2 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0030 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0032 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0048 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0049 | 0/0 | 4438 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0050 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0051 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0001t0052 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0004t0015 | 0/0 | 4438 | 4 | 0 | 1 | 0 | 0 | 3 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0004t0023 | 0/0 | 4438 | 2 | 0 | 2 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0001c0004t0029 | 0/0 | 4438 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0002 | 0/0 | 4452 | 35 | 1 | 7 | 20 | 1 | 6 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0003 | 0/0 | 4438 | 25 | 6 | 9 | 8 | 0 | 2 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0004 | 0/0 | 4439 | 20 | 1 | 3 | 11 | 0 | 5 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0006 | 0/0 | 4452 | 11 | 11 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0009 | 0/0 | 4439 | 10 | 7 | 3 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0011 | 0/0 | 4438 | 8 | 6 | 2 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0013 | 0/0 | 4439 | 6 | 0 | 1 | 4 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0014 | 0/0 | 4438 | 4 | 0 | 0 | 4 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0017 | 0/0 | 4452 | 4 | 0 | 0 | 4 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0018 | 0/0 | 4452 | 4 | 0 | 2 | 1 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0019 | 0/0 | 4457 | 3 | 3 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0022 | 0/0 | 4438 | 2 | 2 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0025 | 0/0 | 4452 | 2 | 0 | 0 | 0 | 2 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0031 | 0/0 | 4439 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0033 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0034 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0035 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0036 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0037 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0038 | 0/0 | 4438 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0039 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0040 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0041 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0042 | 0/1 | 4452 | 1 | 0 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0046 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0002t0047 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0005t0020 | 0/0 | 4452 | 3 | 3 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0005t0043 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0005t0044 | 0/0 | 4469 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0002c0005t0045 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0003c0003t0007 | 0/0 | 4452 | 10 | 0 | 3 | 5 | 0 | 2 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0003c0003t0008 | 0/0 | 4452 | 10 | 0 | 0 | 8 | 0 | 2 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0003c0003t0012 | 0/0 | 4452 | 7 | 0 | 5 | 2 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0003c0003t0026 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0003c0003t0027 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0003c0003t0028 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0004c0008t0001 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0005c0006t0005 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| a0006c0007t0001 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | copy fasta | chr22 | 19031286 | 19127412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0016g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0016g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0021g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0021g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0021g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0024g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0024g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0030g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0032g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0048g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0049g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0050g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0051g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0001t0052g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0004t0015g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0004t0015g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0004t0015g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0004t0015g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0004t0023g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0004t0023g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0001c0004t0029g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0011g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0011g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0011g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0011g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0011g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0011g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0011g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0011g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0013g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0013g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0013g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0013g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0014g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0014g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0014g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0014g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0017g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0017g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0017g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0017g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0018g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0018g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0018g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0018g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0019g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0019g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0019g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0022g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0022g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0025g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0025g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0031g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0033g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0034g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0035g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0036g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0037g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0038g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0039g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0040g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0041g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0042g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0046g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0002t0047g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0005t0020g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0005t0020g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0005t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0005t0043g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0005t0044g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0002c0005t0045g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0012g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0012g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0012g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0012g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0012g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0012g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0012g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0026g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0027g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0003c0003t0028g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0004c0008t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0005c0006t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| a0006c0007t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0141 | EUR | FIN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0045 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00438 | hp1 | a0002 | c0002 | t0004 | g0090 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00544 | hp1 | a0002 | c0002 | t0013 | g0082 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00609 | hp2 | a0002 | c0002 | t0036 | g0056 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0159 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00642 | hp1 | a0003 | c0003 | t0012 | g0013 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0060 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00673 | hp2 | a0002 | c0002 | t0013 | g0077 | EAS | CHS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0151 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0170 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0161 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01070 | hp1 | a0002 | c0002 | t0031 | g0063 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01070 | hp2 | a0001 | c0004 | t0023 | g0127 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0162 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01071 | hp2 | a0001 | c0004 | t0023 | g0132 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01081 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01099 | hp1 | a0001 | c0001 | t0016 | g0115 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01099 | hp2 | a0002 | c0002 | t0004 | g0078 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0065 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01109 | hp1 | a0002 | c0002 | t0009 | g0085 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01168 | hp1 | a0001 | c0004 | t0015 | g0128 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01169 | hp1 | a0002 | c0002 | t0018 | g0150 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01192 | hp1 | a0001 | c0001 | t0049 | g0196 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01255 | hp2 | a0002 | c0002 | t0011 | g0328 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0051 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01256 | hp2 | a0003 | c0003 | t0007 | g0012 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01257 | hp2 | a0002 | c0002 | t0009 | g0005 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01258 | hp1 | a0002 | c0002 | t0009 | g0005 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01258 | hp2 | a0003 | c0003 | t0007 | g0026 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01261 | hp1 | a0002 | c0002 | t0011 | g0326 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0149 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01346 | hp2 | a0002 | c0005 | t0044 | g0137 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0055 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0066 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01433 | hp2 | a0002 | c0002 | t0018 | g0158 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01496 | hp1 | a0002 | c0002 | t0013 | g0004 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01515 | hp2 | a0002 | c0002 | t0025 | g0145 | EUR | IBS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01517 | hp1 | a0002 | c0002 | t0025 | g0171 | EUR | IBS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | IBS | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01884 | hp1 | a0002 | c0002 | t0009 | g0126 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01884 | hp2 | a0002 | c0002 | t0003 | g0053 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01891 | hp2 | a0002 | c0002 | t0003 | g0068 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0062 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0175 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01952 | hp2 | a0003 | c0003 | t0007 | g0015 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01975 | hp2 | a0003 | c0003 | t0012 | g0016 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0054 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01993 | hp2 | a0003 | c0003 | t0012 | g0014 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02027 | hp2 | a0003 | c0003 | t0008 | g0019 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02056 | hp2 | a0003 | c0003 | t0028 | g0022 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02080 | hp2 | a0001 | c0001 | t0021 | g0286 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02083 | hp1 | a0003 | c0003 | t0012 | g0025 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02145 | hp1 | a0002 | c0002 | t0006 | g0185 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02148 | hp1 | a0002 | c0002 | t0004 | g0092 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02148 | hp2 | a0003 | c0003 | t0012 | g0017 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | CDX | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02155 | hp2 | a0001 | c0001 | t0021 | g0291 | EAS | CDX | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CDX | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CDX | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02257 | hp1 | a0002 | c0002 | t0006 | g0001 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0072 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02258 | hp1 | a0002 | c0002 | t0006 | g0001 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0073 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02300 | hp1 | a0002 | c0002 | t0004 | g0093 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02300 | hp2 | a0003 | c0003 | t0012 | g0018 | AMR | PEL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0119 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02451 | hp2 | a0002 | c0002 | t0047 | g0325 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | KHV | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02602 | hp2 | a0001 | c0004 | t0015 | g0129 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02615 | hp1 | a0001 | c0001 | t0016 | g0044 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02615 | hp2 | a0002 | c0002 | t0019 | g0088 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02622 | hp1 | a0002 | c0005 | t0043 | g0138 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02622 | hp2 | a0002 | c0002 | t0009 | g0105 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02630 | hp2 | a0001 | c0001 | t0024 | g0111 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02647 | hp1 | a0002 | c0002 | t0009 | g0106 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02647 | hp2 | a0002 | c0002 | t0011 | g0333 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0076 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02698 | hp2 | a0001 | c0004 | t0015 | g0131 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02717 | hp1 | a0002 | c0002 | t0035 | g0095 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0117 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02723 | hp2 | a0002 | c0002 | t0033 | g0107 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02735 | hp1 | a0003 | c0003 | t0007 | g0037 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0148 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02738 | hp2 | a0002 | c0002 | t0004 | g0075 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0120 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02809 | hp2 | a0002 | c0002 | t0006 | g0186 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02818 | hp1 | a0002 | c0002 | t0009 | g0104 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0122 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02886 | hp1 | a0002 | c0005 | t0020 | g0136 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02886 | hp2 | a0001 | c0001 | t0016 | g0114 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0118 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02896 | hp2 | a0002 | c0002 | t0006 | g0187 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0113 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02897 | hp2 | a0002 | c0002 | t0011 | g0329 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02922 | hp1 | a0002 | c0002 | t0011 | g0327 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02922 | hp2 | a0002 | c0002 | t0022 | g0069 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02965 | hp1 | a0002 | c0002 | t0046 | g0324 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02965 | hp2 | a0001 | c0001 | t0048 | g0218 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02970 | hp1 | a0002 | c0002 | t0019 | g0087 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0125 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02976 | hp1 | a0001 | c0001 | t0024 | g0112 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0003 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0124 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03098 | hp1 | a0002 | c0002 | t0011 | g0332 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0123 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03130 | hp2 | a0002 | c0002 | t0006 | g0181 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03139 | hp2 | a0002 | c0005 | t0020 | g0135 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03209 | hp1 | a0001 | c0001 | t0050 | g0334 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03209 | hp2 | a0002 | c0002 | t0040 | g0049 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03225 | hp2 | a0002 | c0005 | t0045 | g0139 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03239 | hp2 | a0001 | c0004 | t0029 | g0043 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03453 | hp1 | a0002 | c0002 | t0011 | g0331 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0167 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03490 | hp2 | a0001 | c0004 | t0015 | g0130 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0169 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03516 | hp2 | a0002 | c0002 | t0037 | g0064 | AFR | ESN | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03540 | hp1 | a0002 | c0002 | t0006 | g0188 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03540 | hp2 | a0002 | c0002 | t0009 | g0084 | AFR | GWD | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03579 | hp1 | a0002 | c0002 | t0006 | g0001 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0089 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03688 | hp1 | a0002 | c0002 | t0004 | g0101 | SAS | STU | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03688 | hp2 | a0003 | c0003 | t0027 | g0035 | SAS | STU | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03710 | hp1 | a0002 | c0002 | t0003 | g0046 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03831 | hp1 | a0003 | c0003 | t0008 | g0010 | SAS | BEB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | BEB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03834 | hp2 | a0003 | c0003 | t0007 | g0027 | SAS | BEB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0154 | SAS | BEB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03942 | hp1 | a0002 | c0002 | t0041 | g0166 | SAS | BEB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0157 | SAS | STU | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG04115 | hp2 | a0002 | c0002 | t0004 | g0094 | SAS | STU | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG04199 | hp1 | a0002 | c0002 | t0018 | g0182 | SAS | STU | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG04199 | hp2 | a0003 | c0003 | t0008 | g0031 | SAS | STU | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | STU | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0155 | SAS | STU | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18522 | hp1 | a0002 | c0002 | t0009 | g0074 | AFR | YRI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18522 | hp2 | a0002 | c0002 | t0011 | g0330 | AFR | YRI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0288 | EAS | CHB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | CHB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18906 | hp1 | a0002 | c0002 | t0019 | g0100 | AFR | YRI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18906 | hp2 | a0002 | c0002 | t0006 | g0179 | AFR | YRI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18940 | hp1 | a0002 | c0002 | t0004 | g0083 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18942 | hp1 | a0002 | c0002 | t0014 | g0042 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18944 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18945 | hp1 | a0004 | c0008 | t0001 | g0292 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18945 | hp2 | a0002 | c0002 | t0017 | g0160 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18946 | hp1 | a0001 | c0001 | t0052 | g0335 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18947 | hp2 | a0002 | c0002 | t0004 | g0098 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18951 | hp1 | a0002 | c0002 | t0004 | g0079 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18956 | hp1 | a0002 | c0002 | t0004 | g0108 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18956 | hp2 | a0003 | c0003 | t0026 | g0009 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18957 | hp2 | a0002 | c0002 | t0034 | g0047 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18960 | hp2 | a0002 | c0002 | t0017 | g0146 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18961 | hp1 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18964 | hp2 | a0003 | c0003 | t0008 | g0023 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18965 | hp2 | a0001 | c0001 | t0051 | g0319 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18971 | hp2 | a0003 | c0003 | t0008 | g0024 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18975 | hp1 | a0002 | c0002 | t0004 | g0099 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18978 | hp2 | a0002 | c0002 | t0014 | g0040 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18981 | hp1 | a0003 | c0003 | t0012 | g0029 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18984 | hp2 | a0003 | c0003 | t0008 | g0011 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18990 | hp1 | a0002 | c0002 | t0004 | g0103 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18997 | hp1 | a0002 | c0002 | t0004 | g0097 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA18997 | hp2 | a0001 | c0001 | t0021 | g0322 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19003 | hp2 | a0006 | c0007 | t0001 | g0281 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19004 | hp1 | a0003 | c0003 | t0007 | g0036 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19005 | hp1 | a0002 | c0002 | t0013 | g0081 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19007 | hp1 | a0002 | c0002 | t0004 | g0096 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19009 | hp1 | a0003 | c0003 | t0007 | g0033 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19010 | hp2 | a0002 | c0002 | t0014 | g0041 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19012 | hp1 | a0003 | c0003 | t0008 | g0021 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19030 | hp1 | a0001 | c0001 | t0032 | g0121 | AFR | LWK | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | LWK | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | LWK | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | LWK | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19056 | hp1 | a0003 | c0003 | t0007 | g0020 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19057 | hp1 | a0005 | c0006 | t0005 | g0193 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19057 | hp2 | a0002 | c0002 | t0004 | g0080 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19060 | hp1 | a0002 | c0002 | t0014 | g0039 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19068 | hp1 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19074 | hp1 | a0003 | c0003 | t0008 | g0030 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19079 | hp1 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19079 | hp2 | a0002 | c0002 | t0017 | g0180 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19084 | hp1 | a0002 | c0002 | t0017 | g0178 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19085 | hp1 | a0003 | c0003 | t0007 | g0028 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19086 | hp1 | a0002 | c0002 | t0013 | g0102 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19088 | hp1 | a0003 | c0003 | t0008 | g0038 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19089 | hp1 | a0003 | c0003 | t0008 | g0032 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19089 | hp2 | a0002 | c0002 | t0018 | g0140 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19090 | hp1 | a0003 | c0003 | t0007 | g0034 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19090 | hp2 | a0002 | c0002 | t0004 | g0091 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19240 | hp1 | a0002 | c0002 | t0022 | g0071 | AFR | YRI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA19240 | hp2 | a0001 | c0001 | t0030 | g0116 | AFR | YRI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | ASW | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA20129 | hp2 | a0002 | c0002 | t0006 | g0184 | AFR | ASW | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA20752 | hp2 | a0002 | c0002 | t0013 | g0004 | EUR | TSI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA20805 | hp2 | a0002 | c0002 | t0038 | g0061 | EUR | TSI | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0251 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02486 | hp1 | a0002 | c0002 | t0006 | g0189 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02486 | hp2 | a0002 | c0002 | t0004 | g0109 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02559 | hp1 | a0002 | c0002 | t0039 | g0110 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG02559 | hp2 | a0002 | c0005 | t0020 | g0191 | AFR | ACB | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0314 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0070 | AFR | MSL | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG06807 | hp1 | a0002 | c0002 | t0009 | g0086 | AFR | USA | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | USA | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | USA | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0176 | AFR | USA | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0042 | g0152 | REF | REF | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0195 | REF | REF | DGCR2_chr22_19031286_19127412 | DGCR2 | chr22 | 19031286 | 19127412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:19039043
|
C | T | 1 | a0006 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1475G>A | p.Arg492His | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1681/4438 | 1475/1653 | 492/550 | chr22 | 19039043 | ||
| chr22:19039100
|
A | G | 1 | a0002 | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
missense_variant | MODERATE | c.1418T>C | p.Val473Ala | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1624/4438 | 1418/1653 | 473/550 | chr22 | 19039100 | ||
| chr22:19041130
|
C | T | 1 | a0003 | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
missense_variant | MODERATE | c.1324G>A | p.Gly442Ser | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/10 | 1530/4438 | 1324/1653 | 442/550 | chr22 | 19041130 | ||
| chr22:19041915
|
C | T | 1 | a0005 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1051G>A | p.Val351Ile | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 8/10 | 1257/4438 | 1051/1653 | 351/550 | chr22 | 19041915 | ||
| chr22:19068109
|
G | A | 1 | a0004 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.319C>T | p.Arg107Cys | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/10 | 525/4438 | 319/1653 | 107/550 | chr22 | 19068109 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:19038967
|
C | G | 1 | a0001c0004 | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
synonymous_variant | LOW | c.1551G>C | p.Leu517Leu | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1757/4438 | 1551/1653 | 517/550 | chr22 | 19038967 | ||
| chr22:19064973
|
G | A | 1 | a0002c0005 | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
synonymous_variant | LOW | c.423C>T | p.Ala141Ala | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/10 | 629/4438 | 423/1653 | 141/550 | chr22 | 19064973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:19036462
|
G | A | 1 | a0002c0002t0037 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 2403 | chr22 | 19036462 | |||||
| chr22:19036619
|
G | A | 3 | a0001c0004t0015a0001c0004t0023a0001c0004t0029 | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2246C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 2246 | chr22 | 19036619 | |||||
| chr22:19036688
|
T | C | 1 | a0001c0001t0032 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2177A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 2177 | chr22 | 19036688 | |||||
| chr22:19036724
|
T | TGGCCTGA others(11): Show |
1 | a0002c0005t0044 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123_*2140dupTCCA others(14): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 2140 | chr22 | 19036724 | |||||
| chr22:19036729
|
T | TGAGTGCT others(11): Show |
1 | a0002c0002t0019 | 3 | HG02615.hp2 HG02970.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2118_*2135dupGGGC others(14): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 2135 | chr22 | 19036729 | |||||
| chr22:19036853
|
C | T | 1 | a0001c0001t0051 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2012G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 2012 | chr22 | 19036853 | |||||
| chr22:19036854
|
G | A | 1 | a0002c0002t0035 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2011C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 2011 | chr22 | 19036854 | |||||
| chr22:19036908
|
G | A | 1 | a0001c0001t0050 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1957C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1957 | chr22 | 19036908 | |||||
| chr22:19036999
|
G | A | 1 | a0002c0002t0036 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1866C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1866 | chr22 | 19036999 | |||||
| chr22:19037097
|
G | A | 6 | a0001c0001t0021a0002c0002t0037a0002c0002t0046others(3): Show | 17 | HG02027.hp2 HG02056.hp2 HG02080.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1768C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1768 | chr22 | 19037097 | |||||
| chr22:19037138
|
C | T | 33 | a0001c0001t0005a0001c0001t0010a0001c0001t0030others(30): Show | 187 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*1727G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1727 | chr22 | 19037138 | |||||
| chr22:19037275
|
G | T | 1 | a0001c0001t0049 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1590C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1590 | chr22 | 19037275 | |||||
| chr22:19037301
|
C | A | 1 | a0002c0002t0041 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1564G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1564 | chr22 | 19037301 | |||||
| chr22:19037309
|
G | A | 1 | a0002c0002t0034 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1556C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1556 | chr22 | 19037309 | |||||
| chr22:19037462
|
C | CT | 24 | a0001c0001t0048a0002c0002t0002a0002c0002t0004others(21): Show | 136 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1402_*1403insA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1402 | chr22 | 19037462 | |||||
| chr22:19037466
|
G | A | 1 | a0002c0002t0031 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1399C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1399 | chr22 | 19037466 | |||||
| chr22:19037493
|
C | T | 1 | a0002c0002t0034 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1372G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1372 | chr22 | 19037493 | |||||
| chr22:19037569
|
C | T | 1 | a0002c0002t0025 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1296G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1296 | chr22 | 19037569 | |||||
| chr22:19037817
|
A | C | 6 | a0002c0002t0002a0002c0002t0017a0002c0002t0018others(3): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1048T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1048 | chr22 | 19037817 | |||||
| chr22:19037842
|
C | T | 1 | a0003c0003t0027 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1023G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 1023 | chr22 | 19037842 | |||||
| chr22:19037868
|
C | T | 19 | a0002c0002t0003a0002c0002t0004a0002c0002t0009others(16): Show | 88 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*997G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 997 | chr22 | 19037868 | |||||
| chr22:19037882
|
G | A | 2 | a0002c0005t0020a0002c0005t0045 | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*983C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 983 | chr22 | 19037882 | |||||
| chr22:19038019
|
C | T | 1 | a0002c0002t0033 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*846G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 846 | chr22 | 19038019 | |||||
| chr22:19038067
|
C | T | 1 | a0002c0002t0017 | 4 | NA18945.hp2 NA18960.hp2 NA19079.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*798G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 798 | chr22 | 19038067 | |||||
| chr22:19038215
|
A | G | 3 | a0001c0001t0010a0001c0001t0024a0001c0001t0032 | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*650T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 650 | chr22 | 19038215 | |||||
| chr22:19038253
|
C | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 27 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*612G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 612 | chr22 | 19038253 | |||||
| chr22:19038265
|
G | A | 1 | a0002c0002t0039 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*600C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 600 | chr22 | 19038265 | |||||
| chr22:19038338
|
G | A | 1 | a0002c0002t0040 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 527 | chr22 | 19038338 | |||||
| chr22:19038384
|
C | T | 6 | a0002c0002t0002a0002c0002t0006a0002c0002t0017others(3): Show | 57 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*481G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 481 | chr22 | 19038384 | |||||
| chr22:19038510
|
T | A | 6 | a0003c0003t0007a0003c0003t0008a0003c0003t0012others(3): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*355A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 355 | chr22 | 19038510 | |||||
| chr22:19038512
|
A | G | 43 | a0001c0001t0010a0001c0001t0024a0001c0001t0030others(40): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*353T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 353 | chr22 | 19038512 | |||||
| chr22:19038781
|
A | G | 3 | a0001c0004t0015a0001c0004t0023a0001c0004t0029 | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*84T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 84 | chr22 | 19038781 | |||||
| chr22:19038819
|
A | G | 1 | a0001c0001t0030 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*46T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 46 | chr22 | 19038819 | |||||
| chr22:19038824
|
A | G | 1 | a0002c0002t0022 | 2 | HG02922.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*41T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 10/10 | 41 | chr22 | 19038824 | |||||
| chr22:19122234
|
G | GGCTGCGT others(6): Show |
17 | a0002c0002t0002a0002c0002t0006a0002c0002t0017others(14): Show | 94 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
5_prime_UTR_variant | MODIFIER | c.-29_-28insGGGGTCAC others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | 29 | chr22 | 19122234 | |||||
| chr22:19122240
|
A | G | 41 | a0001c0001t0010a0001c0001t0016a0001c0001t0024others(38): Show | 196 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-34T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | 34 | chr22 | 19122240 | |||||
| chr22:19122251
|
A | G | 41 | a0001c0001t0010a0001c0001t0016a0001c0001t0024others(38): Show | 196 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-45T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | 45 | chr22 | 19122251 | |||||
| chr22:19122299
|
A | G | 41 | a0001c0001t0010a0001c0001t0016a0001c0001t0024others(38): Show | 196 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-93T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | 93 | chr22 | 19122299 | |||||
| chr22:19122375
|
C | T | 1 | a0001c0004t0029 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-169G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | 169 | chr22 | 19122375 | |||||
| chr22:19122388
|
C | T | 1 | a0002c0002t0014 | 4 | NA18942.hp1 NA18978.hp2 NA19010.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-182G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | 182 | chr22 | 19122388 | |||||
| chr22:19122389
|
A | T | 5 | a0003c0003t0007a0003c0003t0008a0003c0003t0012others(2): Show | 29 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-183T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | 183 | chr22 | 19122389 | |||||
| chr22:19122390
|
C | T | 1 | a0003c0003t0026 | 1 | NA18956.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-184G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | chr22 | 19122390 | ||||||
| chr22:19122392
|
G | A | 1 | a0001c0001t0052 | 1 | NA18946.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-186C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/10 | chr22 | 19122392 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:19039159
|
G | A | 1 | a0003c0003t0008g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1397-38C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039159 | ||||||
| chr22:19039191
|
C | T | 14 | a0002c0002t0003g0072a0002c0002t0003g0073a0002c0002t0009g0005others(11): Show | 15 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1397-70G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039191 | ||||||
| chr22:19039201
|
A | G | 2 | a0003c0003t0008g0023a0003c0003t0008g0024 | 2 | NA18964.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1397-80T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039201 | ||||||
| chr22:19039364
|
C | A | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1397-243G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039364 | ||||||
| chr22:19039426
|
G | C | 1 | a0001c0001t0001g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1397-305C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039426 | ||||||
| chr22:19039587
|
C | T | 6 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397-466G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039587 | ||||||
| chr22:19039588
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1397-467C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039588 | ||||||
| chr22:19039596
|
G | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1397-475C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039596 | ||||||
| chr22:19039616
|
C | T | 60 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(57): Show | 63 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.1397-495G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039616 | ||||||
| chr22:19039670
|
T | C | 6 | a0003c0003t0007g0015a0003c0003t0012g0013a0003c0003t0012g0014others(3): Show | 6 | HG00642.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397-549A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039670 | ||||||
| chr22:19039723
|
TTTTTC | T | 4 | a0002c0002t0003g0003a0002c0002t0003g0070a0002c0002t0022g0069others(1): Show | 5 | HG01243.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1397-607_1397-603d others(7): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039723 | ||||||
| chr22:19039874
|
G | A | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-753C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039874 | ||||||
| chr22:19039899
|
AAGG | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1397-781_1397-779d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039899 | ||||||
| chr22:19039943
|
G | A | 1 | a0002c0002t0042g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1397-822C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19039943 | ||||||
| chr22:19040007
|
T | A | 1 | a0001c0001t0001g0316 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1397-886A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040007 | ||||||
| chr22:19040053
|
A | G | 1 | a0001c0001t0049g0196 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1397-932T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040053 | ||||||
| chr22:19040069
|
G | A | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1397-948C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040069 | ||||||
| chr22:19040084
|
C | T | 176 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(173): Show | 183 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1397-963G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040084 | ||||||
| chr22:19040355
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1396+703C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040355 | ||||||
| chr22:19040447
|
G | C | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396+611C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040447 | ||||||
| chr22:19040490
|
G | A | 1 | a0001c0001t0005g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1396+568C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040490 | ||||||
| chr22:19040664
|
A | T | 1 | a0002c0002t0017g0178 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1396+394T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040664 | ||||||
| chr22:19040729
|
CACT | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1396+326_1396+328d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040729 | ||||||
| chr22:19040805
|
G | C | 1 | a0002c0002t0037g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1396+253C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040805 | ||||||
| chr22:19040806
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1396+252C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040806 | ||||||
| chr22:19040807
|
C | G | 176 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(173): Show | 183 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1396+251G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040807 | ||||||
| chr22:19040949
|
G | A | 31 | a0002c0005t0020g0191a0003c0003t0007g0012a0003c0003t0007g0015others(28): Show | 31 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.1396+109C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040949 | ||||||
| chr22:19040963
|
T | C | 195 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(192): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1396+95A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040963 | ||||||
| chr22:19040967
|
T | C | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1396+91A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19040967 | ||||||
| chr22:19041003
|
C | A | 1 | a0001c0001t0016g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1396+55G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 9/9 | chr22 | 19041003 | ||||||
| chr22:19041305
|
A | G | 1 | a0002c0002t0009g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1160-11T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 8/9 | chr22 | 19041305 | ||||||
| chr22:19041317
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1160-23G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 8/9 | chr22 | 19041317 | ||||||
| chr22:19041573
|
C | T | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+234G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 8/9 | chr22 | 19041573 | ||||||
| chr22:19041598
|
C | G | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1159+209G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 8/9 | chr22 | 19041598 | ||||||
| chr22:19042029
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1007-70G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042029 | ||||||
| chr22:19042071
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1007-112C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042071 | ||||||
| chr22:19042152
|
A | C | 1 | a0002c0002t0003g0052 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1007-193T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042152 | ||||||
| chr22:19042160
|
G | A | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1007-201C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042160 | ||||||
| chr22:19042299
|
C | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1007-340G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042299 | ||||||
| chr22:19042376
|
C | T | 1 | a0002c0002t0002g0142 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1007-417G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042376 | ||||||
| chr22:19042494
|
A | G | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1007-535T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042494 | ||||||
| chr22:19042562
|
G | A | 6 | a0002c0002t0004g0090a0002c0002t0004g0091a0002c0002t0004g0097others(3): Show | 6 | HG00438.hp1 NA18947.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-603C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042562 | ||||||
| chr22:19042568
|
C | T | 1 | a0002c0002t0013g0081 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1007-609G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042568 | ||||||
| chr22:19042575
|
G | A | 1 | a0001c0001t0032g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1007-616C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042575 | ||||||
| chr22:19042578
|
G | T | 2 | a0001c0001t0010g0124a0001c0001t0010g0125 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1007-619C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042578 | ||||||
| chr22:19042600
|
A | G | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1007-641T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042600 | ||||||
| chr22:19042693
|
C | T | 1 | a0002c0002t0003g0048 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1007-734G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042693 | ||||||
| chr22:19042823
|
A | G | 145 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(142): Show | 152 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.1007-864T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042823 | ||||||
| chr22:19042835
|
T | C | 60 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(57): Show | 63 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.1007-876A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042835 | ||||||
| chr22:19042903
|
G | A | 1 | a0002c0002t0003g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1007-944C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042903 | ||||||
| chr22:19042981
|
ACT | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1007-1024_1007-102 others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19042981 | ||||||
| chr22:19043065
|
G | T | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1007-1106C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043065 | ||||||
| chr22:19043083
|
GGTGAGTA others(4): Show |
G | 1 | a0002c0002t0002g0134 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1007-1135_1007-112 others(15): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043083 | ||||||
| chr22:19043206
|
G | A | 3 | a0002c0002t0002g0151a0002c0002t0002g0159a0002c0002t0002g0170 | 3 | HG00639.hp2 HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1007-1247C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043206 | ||||||
| chr22:19043209
|
A | G | 173 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(170): Show | 180 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.1007-1250T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043209 | ||||||
| chr22:19043319
|
C | G | 100 | a0002c0002t0003g0002a0002c0002t0003g0003a0002c0002t0003g0045others(97): Show | 106 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1007-1360G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043319 | ||||||
| chr22:19043332
|
C | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1007-1373G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043332 | ||||||
| chr22:19043374
|
G | C | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1007-1415C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043374 | ||||||
| chr22:19043412
|
T | TGG | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1007-1455_1007-145 others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043412 | ||||||
| chr22:19043595
|
G | A | 48 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(45): Show | 50 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1007-1636C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043595 | ||||||
| chr22:19043702
|
AC | A | 93 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(90): Show | 97 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1007-1744delG | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043702 | ||||||
| chr22:19043732
|
C | A | 1 | a0002c0002t0003g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1007-1773G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043732 | ||||||
| chr22:19043809
|
C | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1007-1850G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19043809 | ||||||
| chr22:19044101
|
T | C | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1007-2142A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044101 | ||||||
| chr22:19044242
|
G | GCCCAGGG others(2): Show |
3 | a0001c0001t0001g0221a0001c0001t0001g0243a0001c0001t0001g0306 | 3 | HG02074.hp2 HG02165.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1007-2292_1007-228 others(13): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044242 | ||||||
| chr22:19044259
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0243a0001c0001t0001g0306 | 3 | HG02074.hp2 HG02165.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1007-2300C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044259 | ||||||
| chr22:19044296
|
G | A | 1 | a0002c0002t0014g0042 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1007-2337C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044296 | ||||||
| chr22:19044305
|
T | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1007-2346A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044305 | ||||||
| chr22:19044309
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1007-2350C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044309 | ||||||
| chr22:19044377
|
C | G | 1 | a0002c0002t0003g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1007-2418G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044377 | ||||||
| chr22:19044405
|
G | A | 6 | a0002c0002t0004g0090a0002c0002t0004g0091a0002c0002t0004g0097others(3): Show | 6 | HG00438.hp1 NA18947.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-2446C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044405 | ||||||
| chr22:19044546
|
A | AT | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-2588dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044546 | ||||||
| chr22:19044700
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1007-2741T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044700 | ||||||
| chr22:19044701
|
C | A | 1 | a0002c0002t0037g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1007-2742G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044701 | ||||||
| chr22:19044702
|
G | A | 85 | a0002c0002t0003g0002a0002c0002t0003g0003a0002c0002t0003g0045others(82): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1007-2743C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044702 | ||||||
| chr22:19044750
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1007-2791G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044750 | ||||||
| chr22:19044791
|
T | A | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1007-2832A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044791 | ||||||
| chr22:19044841
|
C | A | 1 | a0001c0001t0005g0288 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1007-2882G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044841 | ||||||
| chr22:19044931
|
T | C | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1007-2972A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044931 | ||||||
| chr22:19044989
|
T | C | 2 | a0002c0002t0033g0107a0002c0002t0039g0110 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1007-3030A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044989 | ||||||
| chr22:19044996
|
GT | G | 195 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(192): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1007-3038delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19044996 | ||||||
| chr22:19045081
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1007-3122T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045081 | ||||||
| chr22:19045133
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1007-3174G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045133 | ||||||
| chr22:19045150
|
T | C | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1007-3191A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045150 | ||||||
| chr22:19045365
|
T | TAAAC | 176 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(173): Show | 183 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1006+3071_1006+307 others(8): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045365 | ||||||
| chr22:19045452
|
C | T | 176 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(173): Show | 183 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1006+2988G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045452 | ||||||
| chr22:19045461
|
C | T | 2 | a0003c0003t0008g0023a0003c0003t0008g0024 | 2 | NA18964.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1006+2979G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045461 | ||||||
| chr22:19045739
|
C | T | 2 | a0002c0002t0002g0175a0002c0002t0002g0176 | 2 | HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1006+2701G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045739 | ||||||
| chr22:19045796
|
A | G | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1006+2644T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045796 | ||||||
| chr22:19045840
|
C | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1006+2600G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045840 | ||||||
| chr22:19045894
|
T | A | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1006+2546A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045894 | ||||||
| chr22:19045930
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1006+2510C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045930 | ||||||
| chr22:19045934
|
G | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1006+2506C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19045934 | ||||||
| chr22:19046019
|
T | C | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1006+2421A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046019 | ||||||
| chr22:19046234
|
AT | A | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1006+2205delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046234 | ||||||
| chr22:19046255
|
G | C | 85 | a0002c0002t0003g0002a0002c0002t0003g0003a0002c0002t0003g0045others(82): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1006+2185C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046255 | ||||||
| chr22:19046300
|
A | G | 2 | a0002c0002t0004g0092a0002c0002t0004g0093 | 2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1006+2140T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046300 | ||||||
| chr22:19046395
|
T | G | 2 | a0002c0002t0004g0078a0002c0002t0004g0109 | 2 | HG01099.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1006+2045A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046395 | ||||||
| chr22:19046399
|
T | C | 1 | a0002c0002t0011g0328 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1006+2041A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046399 | ||||||
| chr22:19046566
|
A | C | 91 | a0002c0002t0003g0002a0002c0002t0003g0003a0002c0002t0003g0045others(88): Show | 95 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1006+1874T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046566 | ||||||
| chr22:19046566
|
A | T | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1006+1874T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046566 | ||||||
| chr22:19046579
|
A | T | 1 | a0002c0002t0006g0186 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1006+1861T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046579 | ||||||
| chr22:19046727
|
A | G | 195 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(192): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1006+1713T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19046727 | ||||||
| chr22:19047085
|
A | G | 1 | a0001c0001t0016g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1006+1355T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047085 | ||||||
| chr22:19047271
|
A | G | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1006+1169T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047271 | ||||||
| chr22:19047316
|
A | G | 195 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(192): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1006+1124T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047316 | ||||||
| chr22:19047320
|
T | C | 61 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.1006+1120A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047320 | ||||||
| chr22:19047473
|
G | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1006+967C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047473 | ||||||
| chr22:19047556
|
G | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1006+884C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047556 | ||||||
| chr22:19047559
|
A | G | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1006+881T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047559 | ||||||
| chr22:19047822
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1006+618G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047822 | ||||||
| chr22:19047845
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1006+595A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047845 | ||||||
| chr22:19047894
|
A | C | 1 | a0003c0003t0007g0027 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1006+546T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047894 | ||||||
| chr22:19047917
|
C | T | 1 | a0002c0002t0003g0054 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1006+523G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047917 | ||||||
| chr22:19047920
|
G | A | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+520C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047920 | ||||||
| chr22:19047963
|
G | A | 2 | a0002c0002t0017g0178a0002c0002t0017g0180 | 2 | NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1006+477C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047963 | ||||||
| chr22:19047971
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1006+469G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19047971 | ||||||
| chr22:19048003
|
G | A | 2 | a0001c0001t0005g0210a0001c0001t0005g0211 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1006+437C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19048003 | ||||||
| chr22:19048022
|
G | A | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006+418C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19048022 | ||||||
| chr22:19048184
|
T | C | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1006+256A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19048184 | ||||||
| chr22:19048201
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1006+239C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19048201 | ||||||
| chr22:19048210
|
G | A | 22 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(19): Show | 23 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1006+230C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19048210 | ||||||
| chr22:19048319
|
T | C | 4 | a0002c0002t0002g0134a0002c0002t0002g0163a0002c0005t0043g0138others(1): Show | 4 | HG01346.hp2 HG02622.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+121A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19048319 | ||||||
| chr22:19048331
|
G | A | 1 | a0002c0002t0002g0167 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1006+109C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19048331 | ||||||
| chr22:19048333
|
T | C | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+107A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 7/9 | chr22 | 19048333 | ||||||
| chr22:19048719
|
A | G | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.803-76T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19048719 | ||||||
| chr22:19048919
|
C | T | 3 | a0002c0002t0009g0084a0002c0002t0009g0085a0002c0002t0009g0126 | 3 | HG01109.hp1 HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.803-276G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19048919 | ||||||
| chr22:19048942
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.803-299C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19048942 | ||||||
| chr22:19048966
|
C | T | 195 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(192): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.803-323G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19048966 | ||||||
| chr22:19049131
|
T | C | 2 | a0002c0002t0009g0085a0002c0002t0009g0126 | 2 | HG01109.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.803-488A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049131 | ||||||
| chr22:19049226
|
G | C | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.803-583C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049226 | ||||||
| chr22:19049241
|
G | A | 26 | a0002c0002t0004g0075a0002c0002t0004g0076a0002c0002t0004g0078others(23): Show | 27 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.803-598C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049241 | ||||||
| chr22:19049242
|
T | C | 8 | a0001c0001t0001g0225a0001c0001t0001g0294a0001c0001t0001g0302others(5): Show | 8 | HG00597.hp1 HG00621.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.803-599A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049242 | ||||||
| chr22:19049381
|
A | T | 2 | a0003c0003t0008g0023a0003c0003t0008g0024 | 2 | NA18964.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.803-738T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049381 | ||||||
| chr22:19049386
|
A | C | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-743T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049386 | ||||||
| chr22:19049403
|
C | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.803-760G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049403 | ||||||
| chr22:19049437
|
A | G | 3 | a0002c0002t0002g0154a0002c0002t0002g0155a0002c0002t0002g0157 | 3 | HG03927.hp1 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.803-794T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049437 | ||||||
| chr22:19049592
|
C | T | 3 | a0001c0001t0001g0283a0001c0001t0005g0209a0001c0001t0005g0279 | 3 | HG03453.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.803-949G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049592 | ||||||
| chr22:19049749
|
C | T | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.803-1106G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049749 | ||||||
| chr22:19049826
|
C | CA | 6 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0280others(3): Show | 6 | HG02965.hp2 HG03017.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-1184dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049826 | ||||||
| chr22:19049826
|
CA | C | 63 | a0001c0001t0010g0122a0001c0004t0015g0128a0001c0004t0015g0129others(60): Show | 66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.803-1184delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049826 | ||||||
| chr22:19049826
|
CAA | C | 123 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(120): Show | 127 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.803-1185_803-1184d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049826 | ||||||
| chr22:19049870
|
C | A | 1 | a0002c0002t0002g0169 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.803-1227G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049870 | ||||||
| chr22:19049928
|
T | C | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-1285A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049928 | ||||||
| chr22:19049939
|
GAATGAAC others(3): Show |
G | 1 | a0001c0001t0001g0307 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.803-1306_803-1297d others(12): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049939 | ||||||
| chr22:19049982
|
C | T | 1 | a0001c0004t0015g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.803-1339G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19049982 | ||||||
| chr22:19050022
|
T | C | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.803-1379A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050022 | ||||||
| chr22:19050060
|
C | G | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-1417G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050060 | ||||||
| chr22:19050061
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.803-1418C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050061 | ||||||
| chr22:19050172
|
T | C | 21 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0142others(18): Show | 22 | HG00558.hp2 HG00597.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.803-1529A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050172 | ||||||
| chr22:19050221
|
G | A | 61 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.803-1578C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050221 | ||||||
| chr22:19050237
|
G | A | 1 | a0002c0002t0002g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.803-1594C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050237 | ||||||
| chr22:19050739
|
G | A | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-2096C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050739 | ||||||
| chr22:19050742
|
C | G | 4 | a0002c0002t0002g0006a0002c0002t0002g0172a0002c0002t0002g0173others(1): Show | 5 | NA18950.hp1 NA18957.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-2099G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050742 | ||||||
| chr22:19050777
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.803-2134A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050777 | ||||||
| chr22:19050925
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.803-2282C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19050925 | ||||||
| chr22:19051136
|
C | A | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-2493G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051136 | ||||||
| chr22:19051188
|
C | CA | 95 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0214others(92): Show | 99 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.803-2546dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051188 | ||||||
| chr22:19051188
|
C | CAA | 48 | a0001c0001t0001g0215a0001c0001t0001g0296a0001c0001t0010g0120others(45): Show | 49 | HG00609.hp2 HG00642.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.803-2547_803-2546d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051188 | ||||||
| chr22:19051188
|
CA | C | 15 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0001t0001g0294others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.803-2546delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051188 | ||||||
| chr22:19051188
|
CAAAAAAA others(4): Show |
C | 10 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(7): Show | 10 | HG02451.hp1 HG02630.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-2556_803-2546d others(13): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051188 | ||||||
| chr22:19051334
|
C | T | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.803-2691G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051334 | ||||||
| chr22:19051386
|
A | G | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.803-2743T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051386 | ||||||
| chr22:19051759
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.803-3116G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051759 | ||||||
| chr22:19051885
|
T | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.803-3242A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051885 | ||||||
| chr22:19051925
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0052g0335 | 2 | NA18946.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.803-3282A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051925 | ||||||
| chr22:19051978
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.803-3335C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19051978 | ||||||
| chr22:19052029
|
T | C | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.803-3386A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052029 | ||||||
| chr22:19052143
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.803-3500C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052143 | ||||||
| chr22:19052193
|
G | T | 85 | a0002c0002t0003g0002a0002c0002t0003g0003a0002c0002t0003g0045others(82): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.803-3550C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052193 | ||||||
| chr22:19052214
|
C | T | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-3571G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052214 | ||||||
| chr22:19052245
|
A | G | 194 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(191): Show | 201 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.803-3602T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052245 | ||||||
| chr22:19052281
|
TG | T | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.803-3639delC | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052281 | ||||||
| chr22:19052398
|
A | C | 1 | a0002c0005t0045g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.803-3755T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052398 | ||||||
| chr22:19052414
|
T | TCA | 25 | a0001c0001t0001g0197a0001c0001t0001g0202a0001c0001t0001g0203others(22): Show | 25 | HG00597.hp1 HG00621.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-3773_803-3772d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052414 | ||||||
| chr22:19052414
|
T | TCACA | 112 | a0001c0004t0023g0127a0001c0004t0023g0132a0002c0002t0002g0006others(109): Show | 118 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.803-3775_803-3772d others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052414 | ||||||
| chr22:19052414
|
T | TCACACA | 55 | a0002c0002t0002g0165a0002c0002t0003g0002a0002c0002t0003g0045others(52): Show | 56 | HG00423.hp2 HG00609.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.803-3777_803-3772d others(8): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052414 | ||||||
| chr22:19052414
|
T | TCACACAC others(1): Show |
4 | a0002c0002t0002g0141a0002c0002t0003g0057a0003c0003t0007g0034others(1): Show | 4 | HG00323.hp2 NA18961.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-3779_803-3772d others(10): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052414 | ||||||
| chr22:19052414
|
T | TCACACAC others(3): Show |
1 | a0002c0002t0037g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.803-3781_803-3772d others(12): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052414 | ||||||
| chr22:19052414
|
TCACACA | T | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-3777_803-3772d others(8): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052414 | ||||||
| chr22:19052451
|
A | G | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.803-3808T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052451 | ||||||
| chr22:19052452
|
G | A | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.803-3809C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052452 | ||||||
| chr22:19052567
|
G | A | 3 | a0001c0004t0015g0128a0001c0004t0015g0130a0001c0004t0015g0131 | 3 | HG01168.hp1 HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.803-3924C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052567 | ||||||
| chr22:19052609
|
CA | C | 139 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(136): Show | 146 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.803-3967delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052609 | ||||||
| chr22:19052644
|
A | G | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.803-4001T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052644 | ||||||
| chr22:19052768
|
G | T | 2 | a0002c0005t0020g0135a0002c0005t0020g0136 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.803-4125C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052768 | ||||||
| chr22:19052778
|
A | AG | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.803-4136dupC | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052778 | ||||||
| chr22:19052840
|
A | G | 2 | a0002c0002t0004g0092a0002c0002t0004g0093 | 2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.802+4146T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052840 | ||||||
| chr22:19052876
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.802+4110T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052876 | ||||||
| chr22:19052896
|
C | T | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.802+4090G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052896 | ||||||
| chr22:19052933
|
C | T | 60 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(57): Show | 63 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.802+4053G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19052933 | ||||||
| chr22:19053262
|
A | G | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.802+3724T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053262 | ||||||
| chr22:19053295
|
T | A | 60 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(57): Show | 63 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.802+3691A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053295 | ||||||
| chr22:19053307
|
T | A | 1 | a0003c0003t0012g0018 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.802+3679A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053307 | ||||||
| chr22:19053365
|
A | G | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.802+3621T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053365 | ||||||
| chr22:19053430
|
G | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.802+3556C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053430 | ||||||
| chr22:19053463
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.802+3523C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053463 | ||||||
| chr22:19053468
|
C | T | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.802+3518G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053468 | ||||||
| chr22:19053493
|
A | G | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+3493T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053493 | ||||||
| chr22:19053527
|
G | A | 2 | a0002c0002t0004g0091a0002c0002t0004g0098 | 2 | NA18947.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.802+3459C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053527 | ||||||
| chr22:19053576
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.802+3410G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053576 | ||||||
| chr22:19053586
|
G | C | 3 | a0001c0004t0015g0128a0001c0004t0015g0130a0001c0004t0015g0131 | 3 | HG01168.hp1 HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.802+3400C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053586 | ||||||
| chr22:19053779
|
T | C | 1 | a0002c0005t0045g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.802+3207A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053779 | ||||||
| chr22:19053837
|
G | T | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+3149C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053837 | ||||||
| chr22:19053838
|
A | T | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+3148T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19053838 | ||||||
| chr22:19054186
|
G | A | 85 | a0002c0002t0003g0002a0002c0002t0003g0003a0002c0002t0003g0045others(82): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.802+2800C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054186 | ||||||
| chr22:19054227
|
G | GT | 85 | a0002c0002t0003g0002a0002c0002t0003g0003a0002c0002t0003g0045others(82): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.802+2758_802+2759i others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054227 | ||||||
| chr22:19054238
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+2748G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054238 | ||||||
| chr22:19054250
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.802+2736C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054250 | ||||||
| chr22:19054310
|
T | A | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.802+2676A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054310 | ||||||
| chr22:19054341
|
T | C | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.802+2645A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054341 | ||||||
| chr22:19054383
|
C | A | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.802+2603G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054383 | ||||||
| chr22:19054444
|
A | C | 1 | a0002c0002t0004g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.802+2542T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054444 | ||||||
| chr22:19054447
|
C | T | 6 | a0002c0002t0003g0003a0002c0002t0003g0070a0002c0002t0003g0072others(3): Show | 7 | HG01243.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+2539G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054447 | ||||||
| chr22:19054681
|
T | C | 1 | a0001c0001t0005g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802+2305A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054681 | ||||||
| chr22:19054741
|
T | TA | 134 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0141others(131): Show | 141 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.802+2244dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054741 | ||||||
| chr22:19054762
|
G | A | 4 | a0002c0002t0004g0079a0002c0002t0004g0080a0002c0002t0004g0083others(1): Show | 4 | HG00544.hp1 NA18940.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+2224C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19054762 | ||||||
| chr22:19055029
|
C | T | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.802+1957G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055029 | ||||||
| chr22:19055180
|
T | G | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+1806A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055180 | ||||||
| chr22:19055232
|
T | C | 2 | a0003c0003t0007g0012a0003c0003t0007g0026 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.802+1754A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055232 | ||||||
| chr22:19055309
|
G | A | 146 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.802+1677C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055309 | ||||||
| chr22:19055333
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.802+1653G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055333 | ||||||
| chr22:19055337
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.802+1649C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055337 | ||||||
| chr22:19055470
|
T | G | 1 | a0002c0002t0004g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.802+1516A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055470 | ||||||
| chr22:19055495
|
T | C | 1 | a0002c0005t0045g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.802+1491A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055495 | ||||||
| chr22:19055548
|
G | GTAAA | 32 | a0001c0001t0005g0210a0001c0001t0005g0211a0003c0003t0007g0012others(29): Show | 32 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.802+1434_802+1437d others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055548 | ||||||
| chr22:19055596
|
T | C | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+1390A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055596 | ||||||
| chr22:19055700
|
T | C | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.802+1286A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055700 | ||||||
| chr22:19055786
|
G | A | 48 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(45): Show | 50 | HG00438.hp1 HG01109.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.802+1200C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19055786 | ||||||
| chr22:19056174
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0284a0001c0001t0001g0285others(11): Show | 15 | HG00673.hp1 HG01496.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.802+812C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056174 | ||||||
| chr22:19056189
|
C | A | 1 | a0001c0001t0010g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.802+797G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056189 | ||||||
| chr22:19056225
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.802+761C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056225 | ||||||
| chr22:19056245
|
G | A | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.802+741C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056245 | ||||||
| chr22:19056246
|
C | T | 5 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0005g0262others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.802+740G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056246 | ||||||
| chr22:19056302
|
G | A | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+684C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056302 | ||||||
| chr22:19056554
|
T | C | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.802+432A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056554 | ||||||
| chr22:19056554
|
TA | T | 29 | a0001c0001t0001g0008a0001c0001t0001g0214a0001c0001t0001g0215others(26): Show | 30 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.802+431delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056554 | ||||||
| chr22:19056564
|
A | ACAC | 6 | a0002c0002t0002g0157a0002c0002t0003g0045a0002c0002t0003g0048others(3): Show | 6 | HG00423.hp2 HG00609.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+421_802+422ins others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056564 | ||||||
| chr22:19056566
|
A | AAC | 98 | a0002c0002t0002g0134a0002c0002t0002g0141a0002c0002t0002g0148others(95): Show | 103 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.802+418_802+419dup others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056566 | ||||||
| chr22:19056566
|
A | AC | 8 | a0001c0001t0001g0234a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+419_802+420ins others(1): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056566 | ||||||
| chr22:19056566
|
A | ACAC | 38 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0142others(35): Show | 40 | HG00558.hp2 HG00597.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.802+419_802+420ins others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056566 | ||||||
| chr22:19056566
|
A | C | 9 | a0001c0001t0001g0317a0001c0001t0030g0116a0002c0002t0002g0157others(6): Show | 9 | HG00423.hp2 HG00609.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+420T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056566 | ||||||
| chr22:19056616
|
G | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.802+370C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056616 | ||||||
| chr22:19056704
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.802+282A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056704 | ||||||
| chr22:19056749
|
C | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0272a0001c0001t0001g0273others(24): Show | 28 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.802+237G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056749 | ||||||
| chr22:19056854
|
T | A | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+132A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056854 | ||||||
| chr22:19056907
|
G | A | 2 | a0002c0002t0004g0094a0002c0002t0004g0101 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.802+79C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056907 | ||||||
| chr22:19056965
|
C | T | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.802+21G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 6/9 | chr22 | 19056965 | ||||||
| chr22:19057452
|
C | T | 3 | a0001c0001t0005g0213a0001c0001t0005g0217a0001c0001t0005g0238 | 3 | HG02280.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.626-290G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19057452 | ||||||
| chr22:19057496
|
A | G | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.626-334T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19057496 | ||||||
| chr22:19057761
|
C | CCTGT | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.626-600_626-599ins others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19057761 | ||||||
| chr22:19057812
|
C | A | 1 | a0002c0002t0017g0180 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.626-650G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19057812 | ||||||
| chr22:19058115
|
GCT | G | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.626-955_626-954del others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058115 | ||||||
| chr22:19058187
|
G | A | 1 | a0002c0002t0013g0102 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.626-1025C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058187 | ||||||
| chr22:19058213
|
C | T | 19 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.626-1051G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058213 | ||||||
| chr22:19058271
|
A | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.626-1109T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058271 | ||||||
| chr22:19058356
|
T | C | 1 | a0001c0001t0024g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626-1194A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058356 | ||||||
| chr22:19058419
|
A | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.626-1257T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058419 | ||||||
| chr22:19058422
|
G | A | 2 | a0002c0002t0002g0175a0002c0002t0002g0176 | 2 | HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.626-1260C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058422 | ||||||
| chr22:19058496
|
G | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.626-1334C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058496 | ||||||
| chr22:19058780
|
C | T | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-1618G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058780 | ||||||
| chr22:19058819
|
C | A | 2 | a0001c0001t0024g0111a0001c0001t0024g0112 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.626-1657G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058819 | ||||||
| chr22:19058919
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.626-1757G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058919 | ||||||
| chr22:19058982
|
G | A | 2 | a0003c0003t0008g0023a0003c0003t0008g0024 | 2 | NA18964.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.626-1820C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058982 | ||||||
| chr22:19058990
|
A | G | 2 | a0001c0001t0010g0113a0001c0001t0010g0118 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.626-1828T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19058990 | ||||||
| chr22:19059164
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.626-2002C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059164 | ||||||
| chr22:19059222
|
A | G | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.626-2060T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059222 | ||||||
| chr22:19059244
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.626-2082C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059244 | ||||||
| chr22:19059275
|
C | T | 1 | a0002c0002t0042g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.626-2113G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059275 | ||||||
| chr22:19059324
|
T | C | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.626-2162A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059324 | ||||||
| chr22:19059430
|
T | A | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.626-2268A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059430 | ||||||
| chr22:19059513
|
C | T | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.626-2351G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059513 | ||||||
| chr22:19059694
|
G | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.626-2532C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059694 | ||||||
| chr22:19059828
|
T | G | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.626-2666A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059828 | ||||||
| chr22:19059843
|
C | G | 1 | a0002c0002t0003g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.626-2681G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059843 | ||||||
| chr22:19059856
|
C | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.626-2694G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059856 | ||||||
| chr22:19059860
|
G | A | 1 | a0002c0002t0002g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.626-2698C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059860 | ||||||
| chr22:19059866
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.626-2704G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059866 | ||||||
| chr22:19059868
|
C | A | 1 | a0001c0001t0050g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.626-2706G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059868 | ||||||
| chr22:19059883
|
C | A | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.626-2721G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059883 | ||||||
| chr22:19059890
|
G | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.626-2728C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059890 | ||||||
| chr22:19059916
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.626-2754A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19059916 | ||||||
| chr22:19060005
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0263 | 2 | HG01109.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.626-2843T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060005 | ||||||
| chr22:19060050
|
C | A | 1 | a0001c0001t0021g0291 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.626-2888G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060050 | ||||||
| chr22:19060066
|
C | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.626-2904G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060066 | ||||||
| chr22:19060069
|
C | T | 1 | a0001c0001t0050g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.626-2907G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060069 | ||||||
| chr22:19060263
|
C | A | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.625+2939G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060263 | ||||||
| chr22:19060386
|
C | T | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.625+2816G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060386 | ||||||
| chr22:19060625
|
G | A | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.625+2577C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060625 | ||||||
| chr22:19060836
|
C | T | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+2366G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060836 | ||||||
| chr22:19060900
|
A | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.625+2302T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060900 | ||||||
| chr22:19060923
|
G | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.625+2279C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060923 | ||||||
| chr22:19060936
|
G | A | 58 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(55): Show | 61 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.625+2266C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060936 | ||||||
| chr22:19060993
|
A | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.625+2209T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19060993 | ||||||
| chr22:19061077
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.625+2125G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19061077 | ||||||
| chr22:19061134
|
T | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.625+2068A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19061134 | ||||||
| chr22:19061150
|
G | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.625+2052C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19061150 | ||||||
| chr22:19061175
|
C | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.625+2027G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19061175 | ||||||
| chr22:19061765
|
T | C | 145 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(142): Show | 152 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.625+1437A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19061765 | ||||||
| chr22:19062005
|
T | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.625+1197A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062005 | ||||||
| chr22:19062088
|
A | G | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.625+1114T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062088 | ||||||
| chr22:19062089
|
T | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.625+1113A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062089 | ||||||
| chr22:19062128
|
G | A | 1 | a0001c0001t0010g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.625+1074C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062128 | ||||||
| chr22:19062144
|
T | C | 49 | a0002c0002t0002g0133a0002c0002t0002g0134a0002c0002t0002g0141others(46): Show | 51 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.625+1058A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062144 | ||||||
| chr22:19062259
|
G | A | 1 | a0002c0002t0035g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.625+943C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062259 | ||||||
| chr22:19062269
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.625+933C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062269 | ||||||
| chr22:19062358
|
G | A | 55 | a0002c0002t0002g0133a0002c0002t0002g0134a0002c0002t0002g0141others(52): Show | 57 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.625+844C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062358 | ||||||
| chr22:19062360
|
G | A | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+842C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062360 | ||||||
| chr22:19062430
|
T | C | 1 | a0002c0002t0002g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.625+772A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062430 | ||||||
| chr22:19062457
|
T | C | 1 | a0002c0002t0002g0165 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.625+745A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062457 | ||||||
| chr22:19062494
|
C | T | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.625+708G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062494 | ||||||
| chr22:19062497
|
A | G | 90 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0172others(87): Show | 95 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.625+705T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062497 | ||||||
| chr22:19062568
|
G | A | 2 | a0002c0002t0002g0159a0002c0002t0002g0170 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.625+634C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062568 | ||||||
| chr22:19062584
|
C | T | 1 | a0002c0005t0045g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.625+618G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062584 | ||||||
| chr22:19062585
|
G | A | 1 | a0002c0002t0006g0185 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.625+617C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062585 | ||||||
| chr22:19062597
|
A | G | 175 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(172): Show | 182 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.625+605T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062597 | ||||||
| chr22:19062684
|
G | A | 5 | a0001c0001t0005g0220a0001c0001t0005g0233a0001c0001t0005g0235others(2): Show | 5 | NA18947.hp1 NA18981.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.625+518C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062684 | ||||||
| chr22:19062759
|
A | G | 2 | a0002c0002t0002g0133a0002c0002t0002g0167 | 2 | HG02074.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.625+443T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062759 | ||||||
| chr22:19062774
|
T | TTCGCATT others(21): Show |
1 | a0002c0002t0042g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.625+427_625+428ins others(28): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062774 | ||||||
| chr22:19062774
|
T | TTCTCTCT others(23): Show |
1 | a0002c0002t0002g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.625+427_625+428ins others(30): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062774 | ||||||
| chr22:19062775
|
G | GCTCTCTC others(11): Show |
1 | a0002c0002t0002g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.625+426_625+427ins others(18): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062775 | ||||||
| chr22:19062775
|
G | GCTCTCTC others(29): Show |
1 | a0002c0002t0018g0140 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.625+426_625+427ins others(36): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062775 | ||||||
| chr22:19062775
|
G | GCTCTCTC others(150): Show |
1 | a0002c0002t0002g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.625+426_625+427ins others(157): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062775 | ||||||
| chr22:19062775
|
G | T | 3 | a0002c0002t0002g0133a0002c0002t0002g0151a0002c0002t0042g0152 | 3 | HG00735.hp1 HG02074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.625+427C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062775 | ||||||
| chr22:19062777
|
T | G | 2 | a0002c0002t0002g0159a0002c0002t0002g0170 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.625+425A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062777 | ||||||
| chr22:19062779
|
A | ACT | 105 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0201others(102): Show | 110 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.625+421_625+422dup others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCT | 5 | a0001c0001t0001g0207a0001c0001t0010g0120a0002c0002t0003g0072others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.625+419_625+422dup others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCT | 14 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(11): Show | 16 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.625+417_625+422dup others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(1): Show |
8 | a0002c0002t0025g0145a0002c0002t0025g0171a0002c0005t0020g0135others(5): Show | 8 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.625+415_625+422dup others(8): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(3): Show |
1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.625+413_625+422dup others(10): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(11): Show |
1 | a0002c0002t0006g0181 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.625+405_625+422dup others(18): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(13): Show |
1 | a0002c0002t0006g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.625+403_625+422dup others(20): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(19): Show |
2 | a0002c0002t0002g0169a0002c0002t0018g0182 | 2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.625+397_625+422dup others(26): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(21): Show |
1 | a0002c0002t0002g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.625+395_625+422dup others(28): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(23): Show |
2 | a0002c0002t0002g0161a0002c0002t0002g0162 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.625+422_625+423ins others(30): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(25): Show |
5 | a0002c0002t0002g0164a0002c0002t0017g0160a0002c0002t0018g0150others(2): Show | 5 | HG01169.hp1 HG01433.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.625+422_625+423ins others(32): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(27): Show |
6 | a0002c0002t0002g0134a0002c0002t0002g0153a0002c0002t0002g0155others(3): Show | 6 | HG00408.hp2 HG04228.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+422_625+423ins others(34): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(29): Show |
1 | a0002c0002t0002g0165 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.625+422_625+423ins others(36): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(31): Show |
6 | a0002c0002t0002g0154a0002c0002t0002g0157a0002c0002t0002g0175others(3): Show | 6 | HG01952.hp1 HG03927.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+422_625+423ins others(38): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | ACTCTCTC others(33): Show |
1 | a0002c0002t0002g0163 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.625+422_625+423ins others(40): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | G | 1 | a0002c0002t0002g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.625+423T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
A | T | 8 | a0002c0002t0002g0133a0002c0002t0002g0141a0002c0002t0002g0149others(5): Show | 8 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.625+423T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062779
|
ACTCT | A | 31 | a0001c0001t0005g0209a0003c0003t0007g0012a0003c0003t0007g0015others(28): Show | 31 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.625+419_625+422del others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062779 | ||||||
| chr22:19062782
|
C | CATTCTCT others(126): Show |
1 | a0002c0002t0002g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.625+419_625+420ins others(133): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062782 | ||||||
| chr22:19062788
|
C | A | 1 | a0002c0002t0002g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.625+414G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062788 | ||||||
| chr22:19062790
|
C | CCTCTCTC others(177): Show |
1 | a0002c0002t0002g0167 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.625+411_625+412ins others(184): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062790 | ||||||
| chr22:19062794
|
C | A | 1 | a0002c0002t0002g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.625+408G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062794 | ||||||
| chr22:19062798
|
C | A | 1 | a0002c0002t0002g0167 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.625+404G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062798 | ||||||
| chr22:19062800
|
C | A | 1 | a0002c0002t0002g0151 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.625+402G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062800 | ||||||
| chr22:19062802
|
C | CTCTCTCT others(33): Show |
3 | a0002c0002t0002g0144a0002c0002t0002g0147a0002c0002t0002g0177 | 3 | HG00558.hp2 NA18946.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.625+399_625+400ins others(40): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062802 | ||||||
| chr22:19062802
|
C | CTCTCTCT others(35): Show |
3 | a0002c0002t0002g0142a0002c0002t0002g0168a0002c0002t0002g0190 | 3 | NA18939.hp2 NA18982.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.625+399_625+400ins others(42): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062802 | ||||||
| chr22:19062802
|
C | CTCTCTCT others(37): Show |
1 | a0002c0002t0002g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.625+399_625+400ins others(44): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062802 | ||||||
| chr22:19062804
|
C | CTCTCTCT others(67): Show |
1 | a0002c0002t0002g0159 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.625+397_625+398ins others(74): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062804 | ||||||
| chr22:19062804
|
C | CTCTCTCT others(161): Show |
1 | a0002c0002t0002g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.625+397_625+398ins others(168): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062804 | ||||||
| chr22:19062808
|
A | C | 2 | a0002c0002t0002g0141a0002c0002t0042g0152 | 2 | HG00323.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.625+394T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062808 | ||||||
| chr22:19062811
|
T | TCTCTCTA others(37): Show |
1 | a0002c0002t0002g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.625+390_625+391ins others(44): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062811 | ||||||
| chr22:19062813
|
C | T | 1 | a0002c0002t0002g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.625+389G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062813 | ||||||
| chr22:19062876
|
C | G | 3 | a0002c0002t0002g0149a0002c0002t0025g0145a0002c0002t0025g0171 | 3 | HG01261.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.625+326G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062876 | ||||||
| chr22:19062952
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.625+250C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19062952 | ||||||
| chr22:19063006
|
C | A | 1 | a0001c0001t0001g0318 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.625+196G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063006 | ||||||
| chr22:19063009
|
C | T | 2 | a0002c0005t0020g0135a0002c0005t0020g0136 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.625+193G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063009 | ||||||
| chr22:19063017
|
G | A | 2 | a0002c0002t0025g0145a0002c0002t0025g0171 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.625+185C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063017 | ||||||
| chr22:19063051
|
G | A | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.625+151C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063051 | ||||||
| chr22:19063055
|
G | A | 1 | a0001c0001t0005g0235 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.625+147C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063055 | ||||||
| chr22:19063086
|
T | TCCATGTC | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.625+115_625+116ins others(7): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063086 | ||||||
| chr22:19063122
|
G | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.625+80C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063122 | ||||||
| chr22:19063147
|
G | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.625+55C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063147 | ||||||
| chr22:19063185
|
A | C | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0005g0262others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.625+17T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063185 | ||||||
| chr22:19063195
|
G | C | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
splice_region_variant&intron_variant | LOW | c.625+7C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 5/9 | chr22 | 19063195 | ||||||
| chr22:19063318
|
G | A | 1 | a0002c0002t0002g0183 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.549-40C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063318 | ||||||
| chr22:19063365
|
A | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.549-87T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063365 | ||||||
| chr22:19063373
|
G | A | 1 | a0002c0002t0035g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.549-95C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063373 | ||||||
| chr22:19063378
|
G | A | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.549-100C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063378 | ||||||
| chr22:19063495
|
C | A | 26 | a0002c0002t0002g0006a0002c0002t0002g0172a0002c0002t0002g0173others(23): Show | 28 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.549-217G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063495 | ||||||
| chr22:19063513
|
A | AT | 69 | a0001c0001t0001g0197a0001c0001t0001g0202a0001c0001t0001g0203others(66): Show | 69 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.549-236dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063513 | ||||||
| chr22:19063513
|
A | ATT | 11 | a0002c0002t0002g0149a0002c0002t0002g0154a0002c0002t0002g0183others(8): Show | 13 | HG01261.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.549-237_549-236dup others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063513 | ||||||
| chr22:19063537
|
G | T | 1 | a0002c0002t0002g0142 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.549-259C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063537 | ||||||
| chr22:19063619
|
G | A | 1 | a0002c0002t0002g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.549-341C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063619 | ||||||
| chr22:19063669
|
T | C | 1 | a0001c0001t0001g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.549-391A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063669 | ||||||
| chr22:19063764
|
C | G | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.549-486G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063764 | ||||||
| chr22:19063849
|
G | A | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.549-571C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063849 | ||||||
| chr22:19063868
|
T | C | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.549-590A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19063868 | ||||||
| chr22:19064185
|
C | T | 1 | a0001c0001t0032g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.548+663G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19064185 | ||||||
| chr22:19064295
|
G | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.548+553C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19064295 | ||||||
| chr22:19064321
|
G | C | 2 | a0002c0002t0025g0145a0002c0002t0025g0171 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.548+527C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19064321 | ||||||
| chr22:19064483
|
C | G | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.548+365G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19064483 | ||||||
| chr22:19064530
|
C | G | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.548+318G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19064530 | ||||||
| chr22:19064642
|
G | C | 3 | a0002c0002t0002g0156a0002c0002t0002g0164a0002c0002t0018g0140 | 3 | HG00408.hp2 NA19080.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.548+206C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19064642 | ||||||
| chr22:19064676
|
C | T | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.548+172G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 4/9 | chr22 | 19064676 | ||||||
| chr22:19065180
|
G | T | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.329-113C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065180 | ||||||
| chr22:19065223
|
T | C | 1 | a0001c0004t0029g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.329-156A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065223 | ||||||
| chr22:19065336
|
C | A | 1 | a0001c0001t0001g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.329-269G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065336 | ||||||
| chr22:19065459
|
T | C | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.329-392A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065459 | ||||||
| chr22:19065503
|
A | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.329-436T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065503 | ||||||
| chr22:19065574
|
A | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0248 | 2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.329-507T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065574 | ||||||
| chr22:19065629
|
G | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.329-562C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065629 | ||||||
| chr22:19065647
|
G | A | 1 | a0002c0002t0040g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.329-580C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065647 | ||||||
| chr22:19065728
|
C | T | 1 | a0002c0002t0002g0168 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.329-661G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065728 | ||||||
| chr22:19065777
|
C | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.329-710G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065777 | ||||||
| chr22:19065893
|
G | T | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.329-826C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065893 | ||||||
| chr22:19065956
|
A | ATG | 146 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.329-891_329-890dup others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065956 | ||||||
| chr22:19065956
|
A | G | 1 | a0002c0002t0018g0182 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.329-889T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065956 | ||||||
| chr22:19065964
|
G | T | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.329-897C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19065964 | ||||||
| chr22:19066045
|
C | A | 1 | a0002c0002t0006g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.329-978G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066045 | ||||||
| chr22:19066178
|
T | C | 3 | a0003c0003t0008g0032a0003c0003t0008g0038a0003c0003t0026g0009 | 3 | NA18956.hp2 NA19088.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.329-1111A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066178 | ||||||
| chr22:19066259
|
G | C | 1 | a0002c0002t0003g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.329-1192C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066259 | ||||||
| chr22:19066278
|
G | A | 1 | a0002c0002t0031g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.329-1211C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066278 | ||||||
| chr22:19066377
|
G | A | 6 | a0001c0001t0050g0334a0002c0002t0011g0327a0002c0002t0011g0328others(3): Show | 6 | HG01255.hp2 HG02897.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-1310C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066377 | ||||||
| chr22:19066414
|
C | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.329-1347G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066414 | ||||||
| chr22:19066433
|
C | A | 1 | a0006c0007t0001g0281 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.329-1366G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066433 | ||||||
| chr22:19066433
|
C | CA | 25 | a0001c0001t0001g0287a0001c0001t0005g0238a0002c0002t0003g0002others(22): Show | 26 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.329-1367dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066433 | ||||||
| chr22:19066504
|
G | C | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.329-1437C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066504 | ||||||
| chr22:19066523
|
C | T | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.329-1456G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066523 | ||||||
| chr22:19066647
|
G | C | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.328+1453C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066647 | ||||||
| chr22:19066702
|
C | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.328+1398G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066702 | ||||||
| chr22:19066780
|
T | C | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.328+1320A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19066780 | ||||||
| chr22:19067077
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.328+1023G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067077 | ||||||
| chr22:19067116
|
A | G | 1 | a0002c0002t0002g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.328+984T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067116 | ||||||
| chr22:19067467
|
T | C | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.328+633A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067467 | ||||||
| chr22:19067499
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.328+601G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067499 | ||||||
| chr22:19067508
|
G | T | 195 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(192): Show | 202 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.328+592C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067508 | ||||||
| chr22:19067553
|
C | T | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.328+547G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067553 | ||||||
| chr22:19067692
|
C | CTAAA | 19 | a0001c0001t0001g0008a0001c0001t0001g0192a0001c0001t0001g0284others(16): Show | 20 | HG00673.hp1 HG01496.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.328+404_328+407dup others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067692 | ||||||
| chr22:19067692
|
C | CTAAATAA others(1): Show |
4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0005g0288others(1): Show | 4 | HG02965.hp2 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+400_328+407dup others(8): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067692 | ||||||
| chr22:19067692
|
CTAAA | C | 48 | a0001c0001t0001g0007a0001c0001t0001g0206a0001c0001t0001g0228others(45): Show | 49 | HG00544.hp2 HG00642.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.328+404_328+407del others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067692 | ||||||
| chr22:19067692
|
CTAAATAA others(1): Show |
C | 86 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0260others(83): Show | 90 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.328+400_328+407del others(8): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067692 | ||||||
| chr22:19067692
|
CTAAATAA others(5): Show |
C | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.328+396_328+407del others(12): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067692 | ||||||
| chr22:19067840
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.328+260C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067840 | ||||||
| chr22:19067920
|
C | A | 1 | a0002c0002t0003g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.328+180G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067920 | ||||||
| chr22:19067938
|
G | A | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+162C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067938 | ||||||
| chr22:19067946
|
G | A | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.328+154C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067946 | ||||||
| chr22:19067959
|
T | G | 2 | a0002c0002t0018g0150a0002c0002t0018g0158 | 2 | HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.328+141A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067959 | ||||||
| chr22:19067993
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.328+107C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19067993 | ||||||
| chr22:19068029
|
T | C | 24 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(21): Show | 25 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.328+71A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 3/9 | chr22 | 19068029 | ||||||
| chr22:19068324
|
G | C | 5 | a0003c0003t0007g0012a0003c0003t0007g0020a0003c0003t0007g0026others(2): Show | 5 | HG01256.hp2 HG01258.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.203-99C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19068324 | ||||||
| chr22:19068325
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.203-100C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19068325 | ||||||
| chr22:19068506
|
C | A | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-281G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19068506 | ||||||
| chr22:19068772
|
T | C | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-547A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19068772 | ||||||
| chr22:19068784
|
G | A | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203-559C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19068784 | ||||||
| chr22:19069015
|
G | A | 1 | a0002c0002t0017g0178 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.203-790C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069015 | ||||||
| chr22:19069063
|
T | C | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.203-838A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069063 | ||||||
| chr22:19069083
|
G | A | 1 | a0002c0002t0017g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.203-858C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069083 | ||||||
| chr22:19069085
|
G | A | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203-860C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069085 | ||||||
| chr22:19069207
|
G | A | 3 | a0001c0001t0010g0123a0001c0001t0010g0124a0001c0001t0010g0125 | 3 | HG02970.hp2 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.203-982C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069207 | ||||||
| chr22:19069402
|
A | G | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.203-1177T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069402 | ||||||
| chr22:19069466
|
C | T | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.203-1241G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069466 | ||||||
| chr22:19069499
|
C | T | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.203-1274G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069499 | ||||||
| chr22:19069562
|
T | C | 2 | a0002c0002t0002g0153a0002c0002t0002g0165 | 2 | NA18964.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.203-1337A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069562 | ||||||
| chr22:19069675
|
A | G | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.203-1450T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069675 | ||||||
| chr22:19069685
|
T | C | 6 | a0002c0002t0003g0003a0002c0002t0003g0070a0002c0002t0003g0072others(3): Show | 7 | HG01243.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-1460A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069685 | ||||||
| chr22:19069749
|
C | G | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.203-1524G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069749 | ||||||
| chr22:19069868
|
G | C | 2 | a0002c0002t0004g0078a0002c0002t0004g0109 | 2 | HG01099.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.203-1643C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19069868 | ||||||
| chr22:19070005
|
C | G | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-1780G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070005 | ||||||
| chr22:19070165
|
G | A | 1 | a0002c0002t0006g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.203-1940C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070165 | ||||||
| chr22:19070210
|
A | G | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.203-1985T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070210 | ||||||
| chr22:19070277
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-2052C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070277 | ||||||
| chr22:19070302
|
T | C | 1 | a0002c0002t0002g0167 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.203-2077A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070302 | ||||||
| chr22:19070346
|
C | T | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.203-2121G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070346 | ||||||
| chr22:19070373
|
T | C | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.203-2148A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070373 | ||||||
| chr22:19070633
|
C | T | 30 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0216others(27): Show | 30 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-2408G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070633 | ||||||
| chr22:19070681
|
C | G | 1 | a0002c0002t0047g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.203-2456G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070681 | ||||||
| chr22:19070814
|
T | C | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-2589A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070814 | ||||||
| chr22:19070880
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.203-2655C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19070880 | ||||||
| chr22:19071034
|
C | T | 57 | a0001c0001t0024g0111a0001c0001t0024g0112a0002c0002t0002g0006others(54): Show | 60 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.203-2809G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071034 | ||||||
| chr22:19071234
|
A | C | 1 | a0003c0003t0007g0034 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.203-3009T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071234 | ||||||
| chr22:19071239
|
A | G | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-3014T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071239 | ||||||
| chr22:19071540
|
C | T | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-3315G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071540 | ||||||
| chr22:19071660
|
A | G | 4 | a0002c0002t0014g0039a0002c0002t0014g0040a0002c0002t0014g0041others(1): Show | 4 | NA18942.hp1 NA18978.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-3435T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071660 | ||||||
| chr22:19071765
|
C | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-3540G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071765 | ||||||
| chr22:19071854
|
A | C | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-3629T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071854 | ||||||
| chr22:19071912
|
C | T | 10 | a0002c0002t0003g0003a0002c0002t0003g0070a0002c0002t0003g0072others(7): Show | 11 | HG01243.hp1 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-3687G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071912 | ||||||
| chr22:19071938
|
G | A | 1 | a0001c0001t0010g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.203-3713C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19071938 | ||||||
| chr22:19072011
|
T | C | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.203-3786A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072011 | ||||||
| chr22:19072058
|
G | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.203-3833C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072058 | ||||||
| chr22:19072139
|
G | A | 12 | a0002c0002t0004g0075a0002c0002t0004g0076a0002c0002t0004g0078others(9): Show | 13 | HG00544.hp1 HG00673.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.203-3914C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072139 | ||||||
| chr22:19072142
|
G | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-3917C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072142 | ||||||
| chr22:19072179
|
G | A | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.203-3954C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072179 | ||||||
| chr22:19072248
|
C | T | 3 | a0001c0001t0010g0123a0001c0001t0010g0124a0001c0001t0010g0125 | 3 | HG02970.hp2 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.203-4023G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072248 | ||||||
| chr22:19072375
|
C | T | 7 | a0002c0002t0003g0002a0002c0002t0003g0051a0002c0002t0003g0053others(4): Show | 8 | HG01081.hp1 HG01106.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-4150G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072375 | ||||||
| chr22:19072724
|
A | G | 2 | a0002c0002t0022g0069a0002c0002t0022g0071 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.203-4499T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072724 | ||||||
| chr22:19072890
|
A | T | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.203-4665T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072890 | ||||||
| chr22:19072891
|
T | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0272a0001c0001t0001g0273others(24): Show | 28 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.203-4666A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072891 | ||||||
| chr22:19072899
|
T | A | 68 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(65): Show | 71 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.203-4674A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072899 | ||||||
| chr22:19072900
|
A | T | 33 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0048g0218others(30): Show | 33 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.203-4675T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19072900 | ||||||
| chr22:19073032
|
G | T | 1 | a0002c0002t0003g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.203-4807C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073032 | ||||||
| chr22:19073266
|
C | A | 1 | a0002c0002t0040g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.203-5041G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073266 | ||||||
| chr22:19073266
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0049g0196 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.203-5041G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073266 | ||||||
| chr22:19073268
|
A | C | 2 | a0002c0002t0022g0069a0002c0002t0022g0071 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.203-5043T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073268 | ||||||
| chr22:19073276
|
C | A | 1 | a0002c0002t0002g0183 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.203-5051G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073276 | ||||||
| chr22:19073283
|
CAT | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0272a0001c0001t0001g0273others(24): Show | 28 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.203-5060_203-5059d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073283 | ||||||
| chr22:19073362
|
T | C | 2 | a0002c0002t0033g0107a0002c0002t0039g0110 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.203-5137A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073362 | ||||||
| chr22:19073465
|
T | C | 1 | a0002c0002t0011g0328 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.203-5240A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073465 | ||||||
| chr22:19073531
|
C | T | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-5306G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073531 | ||||||
| chr22:19073724
|
T | G | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-5499A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073724 | ||||||
| chr22:19073817
|
T | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.203-5592A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073817 | ||||||
| chr22:19073818
|
C | T | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203-5593G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073818 | ||||||
| chr22:19073998
|
A | G | 1 | a0001c0001t0010g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.203-5773T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19073998 | ||||||
| chr22:19074014
|
T | C | 15 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(12): Show | 15 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.203-5789A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074014 | ||||||
| chr22:19074165
|
T | C | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.203-5940A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074165 | ||||||
| chr22:19074252
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.203-6027G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074252 | ||||||
| chr22:19074270
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.203-6045T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074270 | ||||||
| chr22:19074357
|
T | C | 1 | a0002c0002t0003g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.203-6132A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074357 | ||||||
| chr22:19074361
|
A | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-6136T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074361 | ||||||
| chr22:19074412
|
G | GA | 14 | a0001c0001t0001g0237a0001c0001t0001g0264a0001c0001t0001g0267others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.203-6188dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074412 | ||||||
| chr22:19074412
|
G | GAA | 6 | a0001c0001t0010g0118a0001c0001t0010g0119a0001c0001t0010g0120others(3): Show | 6 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-6189_203-6188d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074412 | ||||||
| chr22:19074412
|
GA | G | 114 | a0001c0001t0016g0115a0002c0002t0002g0006a0002c0002t0002g0133others(111): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.203-6188delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074412 | ||||||
| chr22:19074412
|
GAA | G | 62 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0051others(59): Show | 65 | HG00438.hp1 HG00544.hp1 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.203-6189_203-6188d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074412 | ||||||
| chr22:19074507
|
A | G | 1 | a0002c0002t0002g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.203-6282T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074507 | ||||||
| chr22:19074547
|
C | T | 3 | a0002c0002t0002g0151a0002c0002t0002g0159a0002c0002t0002g0170 | 3 | HG00639.hp2 HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.203-6322G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074547 | ||||||
| chr22:19074587
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.203-6362C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074587 | ||||||
| chr22:19074697
|
C | T | 1 | a0002c0002t0037g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.203-6472G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074697 | ||||||
| chr22:19074741
|
T | C | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-6516A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074741 | ||||||
| chr22:19074802
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-6577C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074802 | ||||||
| chr22:19074822
|
C | T | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-6597G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074822 | ||||||
| chr22:19074825
|
A | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0252a0001c0001t0001g0271 | 3 | HG00423.hp1 HG01081.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.203-6600T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074825 | ||||||
| chr22:19074840
|
A | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.203-6615T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074840 | ||||||
| chr22:19074952
|
A | G | 1 | a0002c0002t0009g0084 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.203-6727T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19074952 | ||||||
| chr22:19075000
|
A | T | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.203-6775T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075000 | ||||||
| chr22:19075097
|
A | AT | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-6873dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075097 | ||||||
| chr22:19075131
|
A | ACAGTTGG others(94): Show |
1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.203-6907_203-6906i others(103): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075131 | ||||||
| chr22:19075133
|
G | C | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.203-6908C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075133 | ||||||
| chr22:19075166
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.203-6941C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075166 | ||||||
| chr22:19075167
|
C | T | 1 | a0002c0002t0002g0169 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.203-6942G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075167 | ||||||
| chr22:19075253
|
C | T | 1 | a0001c0001t0005g0262 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.203-7028G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075253 | ||||||
| chr22:19075372
|
G | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.203-7147C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075372 | ||||||
| chr22:19075401
|
C | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-7176G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075401 | ||||||
| chr22:19075403
|
T | C | 1 | a0002c0002t0002g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.203-7178A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075403 | ||||||
| chr22:19075446
|
C | CA | 93 | a0001c0001t0001g0267a0001c0001t0050g0334a0002c0002t0003g0003others(90): Show | 96 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.203-7222dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075446 | ||||||
| chr22:19075563
|
G | A | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-7338C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075563 | ||||||
| chr22:19075591
|
T | G | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-7366A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075591 | ||||||
| chr22:19075631
|
T | C | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.203-7406A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075631 | ||||||
| chr22:19075791
|
T | C | 146 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(143): Show | 153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.203-7566A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075791 | ||||||
| chr22:19075810
|
G | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0048g0218 | 3 | HG02965.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.203-7585C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075810 | ||||||
| chr22:19075861
|
G | A | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.203-7636C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19075861 | ||||||
| chr22:19076013
|
C | T | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.203-7788G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076013 | ||||||
| chr22:19076120
|
C | G | 1 | a0002c0002t0018g0140 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.203-7895G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076120 | ||||||
| chr22:19076121
|
A | C | 1 | a0002c0002t0018g0140 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.203-7896T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076121 | ||||||
| chr22:19076121
|
A | G | 176 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(173): Show | 183 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.203-7896T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076121 | ||||||
| chr22:19076141
|
T | TTTTTA | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.203-7917_203-7916i others(7): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076141 | ||||||
| chr22:19076174
|
T | G | 2 | a0001c0001t0024g0111a0001c0001t0024g0112 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.203-7949A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076174 | ||||||
| chr22:19076191
|
T | C | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.203-7966A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076191 | ||||||
| chr22:19076248
|
CCTCCTGG others(132): Show |
C | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-8162_203-8024d others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076248 | ||||||
| chr22:19076412
|
G | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.203-8187C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076412 | ||||||
| chr22:19076432
|
T | A | 2 | a0002c0005t0020g0135a0002c0005t0020g0136 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.203-8207A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076432 | ||||||
| chr22:19076652
|
T | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-8427A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076652 | ||||||
| chr22:19076668
|
C | T | 3 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0308 | 3 | HG00597.hp1 NA19003.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.203-8443G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076668 | ||||||
| chr22:19076724
|
A | AT | 83 | a0001c0001t0001g0194a0001c0001t0001g0212a0001c0001t0001g0219others(80): Show | 88 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.203-8500dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076724 | ||||||
| chr22:19076724
|
A | ATT | 54 | a0001c0001t0001g0234a0001c0001t0001g0311a0001c0001t0010g0125others(51): Show | 55 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.203-8501_203-8500d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076724 | ||||||
| chr22:19076724
|
A | ATTT | 7 | a0002c0002t0002g0151a0002c0002t0002g0157a0002c0002t0002g0161others(4): Show | 7 | HG00735.hp1 HG01069.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.203-8502_203-8500d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076724 | ||||||
| chr22:19076724
|
A | ATTTT | 6 | a0001c0004t0015g0128a0001c0004t0015g0130a0001c0004t0015g0131others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-8503_203-8500d others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076724 | ||||||
| chr22:19076724
|
A | T | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203-8499T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076724 | ||||||
| chr22:19076724
|
AT | A | 48 | a0001c0001t0010g0113a0001c0001t0048g0218a0002c0002t0003g0002others(45): Show | 49 | HG00423.hp2 HG00609.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.203-8500delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076724 | ||||||
| chr22:19076864
|
G | A | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-8639C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076864 | ||||||
| chr22:19076932
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.203-8707C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19076932 | ||||||
| chr22:19077007
|
A | G | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.203-8782T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077007 | ||||||
| chr22:19077233
|
G | C | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-9008C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077233 | ||||||
| chr22:19077253
|
G | C | 1 | a0001c0001t0005g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.203-9028C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077253 | ||||||
| chr22:19077266
|
A | T | 1 | a0001c0001t0005g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.203-9041T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077266 | ||||||
| chr22:19077273
|
T | C | 1 | a0002c0005t0020g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.203-9048A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077273 | ||||||
| chr22:19077327
|
A | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.203-9102T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077327 | ||||||
| chr22:19077458
|
T | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-9233A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077458 | ||||||
| chr22:19077493
|
C | T | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.203-9268G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077493 | ||||||
| chr22:19077586
|
C | T | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.203-9361G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077586 | ||||||
| chr22:19077596
|
A | G | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.203-9371T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077596 | ||||||
| chr22:19077654
|
G | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.203-9429C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077654 | ||||||
| chr22:19077729
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.203-9504A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077729 | ||||||
| chr22:19077781
|
T | G | 1 | a0003c0003t0008g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.203-9556A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077781 | ||||||
| chr22:19077832
|
C | CT | 95 | a0001c0001t0001g0270a0001c0001t0030g0116a0001c0001t0050g0334others(92): Show | 99 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.203-9608dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077832 | ||||||
| chr22:19077890
|
G | A | 1 | a0001c0001t0052g0335 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.203-9665C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077890 | ||||||
| chr22:19077917
|
G | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.203-9692C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077917 | ||||||
| chr22:19077918
|
T | G | 8 | a0001c0001t0001g0208a0001c0001t0001g0216a0001c0001t0001g0222others(5): Show | 8 | HG00544.hp2 HG02027.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-9693A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19077918 | ||||||
| chr22:19078041
|
C | A | 2 | a0002c0002t0002g0161a0002c0002t0002g0162 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.203-9816G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078041 | ||||||
| chr22:19078131
|
T | C | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.203-9906A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078131 | ||||||
| chr22:19078174
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.203-9949C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078174 | ||||||
| chr22:19078226
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.203-10001T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078226 | ||||||
| chr22:19078251
|
C | T | 1 | a0001c0004t0015g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.203-10026G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078251 | ||||||
| chr22:19078252
|
G | A | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.203-10027C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078252 | ||||||
| chr22:19078366
|
CTGAG | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-10145_203-1014 others(8): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078366 | ||||||
| chr22:19078373
|
A | G | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-10148T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078373 | ||||||
| chr22:19078529
|
T | A | 1 | a0001c0001t0001g0311 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.203-10304A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078529 | ||||||
| chr22:19078530
|
A | T | 1 | a0001c0001t0001g0311 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.203-10305T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078530 | ||||||
| chr22:19078658
|
G | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0005g0262others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-10433C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078658 | ||||||
| chr22:19078700
|
C | T | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.203-10475G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078700 | ||||||
| chr22:19078702
|
T | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.203-10477A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078702 | ||||||
| chr22:19078709
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.203-10484T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078709 | ||||||
| chr22:19078854
|
A | G | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+10514T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078854 | ||||||
| chr22:19078867
|
G | C | 1 | a0001c0001t0010g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.202+10501C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078867 | ||||||
| chr22:19078961
|
C | G | 1 | a0001c0001t0001g0007 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.202+10407G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19078961 | ||||||
| chr22:19079251
|
C | T | 1 | a0002c0002t0003g0052 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.202+10117G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19079251 | ||||||
| chr22:19079318
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.202+10050T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19079318 | ||||||
| chr22:19079358
|
C | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+10010G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19079358 | ||||||
| chr22:19079411
|
C | T | 3 | a0003c0003t0007g0027a0003c0003t0007g0037a0003c0003t0008g0031 | 3 | HG02735.hp1 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.202+9957G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19079411 | ||||||
| chr22:19079666
|
T | C | 2 | a0002c0002t0025g0145a0002c0002t0025g0171 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.202+9702A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19079666 | ||||||
| chr22:19079863
|
C | A | 2 | a0003c0003t0008g0030a0003c0003t0012g0029 | 2 | NA18981.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.202+9505G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19079863 | ||||||
| chr22:19079982
|
C | T | 6 | a0003c0003t0007g0015a0003c0003t0012g0013a0003c0003t0012g0014others(3): Show | 6 | HG00642.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.202+9386G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19079982 | ||||||
| chr22:19080358
|
C | T | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.202+9010G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19080358 | ||||||
| chr22:19080656
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.202+8712G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19080656 | ||||||
| chr22:19080657
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.202+8711C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19080657 | ||||||
| chr22:19080714
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.202+8654A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19080714 | ||||||
| chr22:19080833
|
C | CA | 6 | a0002c0002t0004g0090a0002c0002t0004g0091a0002c0002t0004g0097others(3): Show | 6 | HG00438.hp1 NA18947.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+8534dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19080833 | ||||||
| chr22:19080863
|
T | C | 1 | a0001c0001t0005g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.202+8505A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19080863 | ||||||
| chr22:19080982
|
C | T | 4 | a0002c0002t0011g0326a0002c0002t0011g0331a0002c0002t0011g0332others(1): Show | 4 | HG01261.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+8386G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19080982 | ||||||
| chr22:19081083
|
C | T | 1 | a0002c0005t0020g0191 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.202+8285G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081083 | ||||||
| chr22:19081129
|
G | A | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.202+8239C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081129 | ||||||
| chr22:19081221
|
T | C | 1 | a0002c0002t0013g0102 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.202+8147A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081221 | ||||||
| chr22:19081228
|
A | G | 1 | a0002c0002t0002g0175 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.202+8140T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081228 | ||||||
| chr22:19081242
|
A | C | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.202+8126T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081242 | ||||||
| chr22:19081251
|
T | C | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.202+8117A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081251 | ||||||
| chr22:19081509
|
T | A | 59 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(56): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.202+7859A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081509 | ||||||
| chr22:19081714
|
G | A | 1 | a0002c0002t0011g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.202+7654C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081714 | ||||||
| chr22:19081772
|
A | C | 2 | a0002c0002t0033g0107a0002c0002t0039g0110 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.202+7596T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081772 | ||||||
| chr22:19081873
|
A | C | 2 | a0002c0002t0018g0150a0002c0002t0018g0158 | 2 | HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.202+7495T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081873 | ||||||
| chr22:19081950
|
T | A | 1 | a0001c0001t0001g0316 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.202+7418A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081950 | ||||||
| chr22:19081950
|
T | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+7418A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081950 | ||||||
| chr22:19081954
|
C | T | 1 | a0002c0002t0004g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.202+7414G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081954 | ||||||
| chr22:19081980
|
C | T | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.202+7388G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19081980 | ||||||
| chr22:19082054
|
G | GT | 15 | a0002c0002t0006g0001a0002c0002t0006g0179a0002c0002t0006g0181others(12): Show | 17 | HG01346.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.202+7313_202+7314i others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082054 | ||||||
| chr22:19082054
|
GGT | G | 9 | a0002c0002t0002g0134a0002c0002t0002g0147a0002c0002t0002g0151others(6): Show | 9 | HG00408.hp2 HG00735.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+7312_202+7313d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082054 | ||||||
| chr22:19082054
|
GGTT | G | 66 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0141others(63): Show | 69 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.202+7311_202+7313d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082054 | ||||||
| chr22:19082055
|
G | T | 72 | a0001c0001t0050g0334a0002c0002t0003g0068a0002c0002t0004g0075others(69): Show | 76 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.202+7313C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082055 | ||||||
| chr22:19082064
|
G | GT | 36 | a0001c0001t0001g0246a0001c0001t0001g0254a0001c0001t0001g0323others(33): Show | 36 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(33): Show |
intron_variant | MODIFIER | c.202+7303dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082064 | ||||||
| chr22:19082064
|
G | T | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.202+7304C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082064 | ||||||
| chr22:19082067
|
T | G | 85 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(82): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.202+7301A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082067 | ||||||
| chr22:19082073
|
T | G | 1 | a0001c0001t0001g0277 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.202+7295A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082073 | ||||||
| chr22:19082078
|
G | T | 1 | a0002c0002t0040g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.202+7290C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082078 | ||||||
| chr22:19082079
|
A | G | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+7289T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082079 | ||||||
| chr22:19082184
|
GACT | G | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.202+7181_202+7183d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082184 | ||||||
| chr22:19082222
|
C | CT | 125 | a0001c0001t0001g0207a0001c0001t0001g0240a0001c0001t0001g0244others(122): Show | 131 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.202+7145dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082222 | ||||||
| chr22:19082222
|
C | CTT | 10 | a0001c0004t0015g0129a0001c0004t0015g0131a0002c0002t0002g0155others(7): Show | 10 | HG02559.hp1 HG02602.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.202+7144_202+7145d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082222 | ||||||
| chr22:19082222
|
C | CTTT | 23 | a0002c0002t0003g0002a0002c0002t0003g0046a0002c0002t0003g0048others(20): Show | 24 | HG00609.hp2 HG00642.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+7143_202+7145d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082222 | ||||||
| chr22:19082222
|
CT | C | 32 | a0001c0001t0001g0266a0001c0001t0001g0284a0001c0001t0005g0205others(29): Show | 32 | HG00639.hp1 HG00642.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.202+7145delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082222 | ||||||
| chr22:19082226
|
T | C | 1 | a0003c0003t0028g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.202+7142A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082226 | ||||||
| chr22:19082227
|
T | C | 28 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(25): Show | 28 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.202+7141A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082227 | ||||||
| chr22:19082228
|
T | C | 1 | a0003c0003t0008g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.202+7140A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082228 | ||||||
| chr22:19082245
|
T | C | 2 | a0001c0001t0024g0111a0001c0001t0024g0112 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.202+7123A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082245 | ||||||
| chr22:19082342
|
T | C | 3 | a0003c0003t0007g0020a0003c0003t0007g0033a0003c0003t0007g0036 | 3 | NA19004.hp1 NA19009.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.202+7026A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082342 | ||||||
| chr22:19082429
|
G | A | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.202+6939C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082429 | ||||||
| chr22:19082471
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.202+6897C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082471 | ||||||
| chr22:19082744
|
G | T | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+6624C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082744 | ||||||
| chr22:19082799
|
A | G | 1 | a0002c0002t0003g0052 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.202+6569T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082799 | ||||||
| chr22:19082830
|
C | T | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.202+6538G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082830 | ||||||
| chr22:19082831
|
G | A | 3 | a0001c0001t0001g0283a0001c0001t0005g0209a0001c0001t0005g0279 | 3 | HG03453.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.202+6537C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082831 | ||||||
| chr22:19082859
|
C | G | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+6509G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082859 | ||||||
| chr22:19082920
|
T | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.202+6448A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082920 | ||||||
| chr22:19082926
|
G | A | 62 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(59): Show | 65 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.202+6442C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19082926 | ||||||
| chr22:19083019
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0230 | 2 | HG00323.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.202+6349C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083019 | ||||||
| chr22:19083086
|
C | CA | 6 | a0001c0001t0001g0204a0001c0001t0005g0205a0002c0002t0014g0039others(3): Show | 6 | HG02071.hp1 HG02523.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+6281dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083086 | ||||||
| chr22:19083086
|
CA | C | 114 | a0001c0001t0001g0212a0001c0001t0051g0319a0002c0002t0002g0006others(111): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.202+6281delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083086 | ||||||
| chr22:19083219
|
T | C | 22 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(19): Show | 23 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.202+6149A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083219 | ||||||
| chr22:19083250
|
T | C | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.202+6118A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083250 | ||||||
| chr22:19083400
|
C | T | 1 | a0003c0003t0008g0030 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.202+5968G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083400 | ||||||
| chr22:19083404
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0229 | 2 | HG02027.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.202+5964A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083404 | ||||||
| chr22:19083419
|
C | A | 2 | a0002c0005t0020g0135a0002c0005t0020g0136 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.202+5949G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083419 | ||||||
| chr22:19083424
|
T | C | 1 | a0002c0002t0006g0187 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.202+5944A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083424 | ||||||
| chr22:19083475
|
C | T | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.202+5893G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083475 | ||||||
| chr22:19083672
|
TCCCCTCT others(14): Show |
T | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.202+5675_202+5695d others(23): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083672 | ||||||
| chr22:19083673
|
C | G | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+5695G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083673 | ||||||
| chr22:19083678
|
C | T | 12 | a0001c0001t0050g0334a0002c0002t0003g0068a0002c0002t0011g0326others(9): Show | 12 | HG01255.hp2 HG01261.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.202+5690G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083678 | ||||||
| chr22:19083692
|
C | CCCCCCCT others(6): Show |
1 | a0002c0002t0002g0165 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.202+5675_202+5676i others(15): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083692 | ||||||
| chr22:19083696
|
C | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+5672G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083696 | ||||||
| chr22:19083706
|
C | CCCCCTCC others(6): Show |
1 | a0002c0002t0002g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.202+5661_202+5662i others(15): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083706 | ||||||
| chr22:19083706
|
C | CCCCTCCC others(6): Show |
1 | a0002c0002t0002g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.202+5661_202+5662i others(15): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083706 | ||||||
| chr22:19083706
|
C | CCCCTCCC others(5): Show |
50 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(47): Show | 53 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.202+5661_202+5662i others(14): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083706 | ||||||
| chr22:19083706
|
C | CCCCTCCC others(6): Show |
1 | a0002c0002t0017g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.202+5661_202+5662i others(15): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083706 | ||||||
| chr22:19083706
|
C | CCCCTCT | 65 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(62): Show | 68 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.202+5656_202+5661d others(8): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083706 | ||||||
| chr22:19083706
|
C | T | 26 | a0002c0002t0002g0165a0002c0002t0003g0002a0002c0002t0003g0045others(23): Show | 27 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.202+5662G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083706 | ||||||
| chr22:19083709
|
CTCTCCCT others(10): Show |
C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+5642_202+5658d others(19): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083709 | ||||||
| chr22:19083722
|
C | T | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.202+5646G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083722 | ||||||
| chr22:19083750
|
G | C | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.202+5618C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083750 | ||||||
| chr22:19083864
|
G | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.202+5504C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083864 | ||||||
| chr22:19083866
|
G | A | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+5502C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083866 | ||||||
| chr22:19083914
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0280a0001c0001t0001g0282 | 3 | HG03017.hp1 HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.202+5454C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19083914 | ||||||
| chr22:19084001
|
C | T | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.202+5367G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084001 | ||||||
| chr22:19084039
|
C | T | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+5329G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084039 | ||||||
| chr22:19084041
|
A | G | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.202+5327T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084041 | ||||||
| chr22:19084114
|
G | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.202+5254C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084114 | ||||||
| chr22:19084161
|
G | T | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+5207C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084161 | ||||||
| chr22:19084177
|
G | A | 85 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(82): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.202+5191C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084177 | ||||||
| chr22:19084180
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.202+5188G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084180 | ||||||
| chr22:19084181
|
G | A | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.202+5187C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084181 | ||||||
| chr22:19084200
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.202+5168C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084200 | ||||||
| chr22:19084358
|
T | C | 1 | a0001c0001t0032g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.202+5010A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084358 | ||||||
| chr22:19084365
|
G | C | 2 | a0001c0004t0023g0127a0001c0004t0023g0132 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.202+5003C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084365 | ||||||
| chr22:19084394
|
C | T | 1 | a0002c0002t0006g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202+4974G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084394 | ||||||
| chr22:19084404
|
G | C | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.202+4964C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084404 | ||||||
| chr22:19084448
|
C | T | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+4920G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084448 | ||||||
| chr22:19084458
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.202+4910C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084458 | ||||||
| chr22:19084469
|
GGCCCCTT others(33): Show |
G | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.202+4859_202+4898d others(42): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084469 | ||||||
| chr22:19084476
|
T | C | 305 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0208others(302): Show | 314 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.202+4892A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084476 | ||||||
| chr22:19084489
|
GCCCCGTC others(73): Show |
G | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.202+4799_202+4878d others(82): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084489 | ||||||
| chr22:19084524
|
C | G | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.202+4844G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084524 | ||||||
| chr22:19084529
|
G | A | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+4839C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084529 | ||||||
| chr22:19084529
|
GCCCCGTC others(33): Show |
G | 84 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(81): Show | 88 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.202+4799_202+4838d others(42): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084529 | ||||||
| chr22:19084569
|
A | G | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.202+4799T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084569 | ||||||
| chr22:19084617
|
T | C | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202+4751A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084617 | ||||||
| chr22:19084637
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.202+4731G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084637 | ||||||
| chr22:19084654
|
ATCCGGGA others(39): Show |
A | 4 | a0002c0002t0017g0146a0002c0002t0017g0160a0002c0002t0017g0178others(1): Show | 4 | NA18945.hp2 NA18960.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+4668_202+4713d others(48): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084654 | ||||||
| chr22:19084668
|
TGGGGGTC others(40): Show |
T | 51 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(48): Show | 54 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.202+4653_202+4699d others(49): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084668 | ||||||
| chr22:19084678
|
C | CCCCCGCC others(10): Show |
1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202+4689_202+4690i others(19): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084678 | ||||||
| chr22:19084694
|
T | C | 141 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(138): Show | 145 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.202+4674A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084694 | ||||||
| chr22:19084694
|
TGCCCCGT others(40): Show |
T | 1 | a0001c0001t0001g0254 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.202+4627_202+4673d others(49): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084694 | ||||||
| chr22:19084704
|
G | A | 62 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(59): Show | 65 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.202+4664C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084704 | ||||||
| chr22:19084734
|
G | A | 64 | a0001c0001t0030g0116a0001c0001t0050g0334a0002c0002t0003g0003others(61): Show | 67 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.202+4634C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084734 | ||||||
| chr22:19084751
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+4617C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084751 | ||||||
| chr22:19084752
|
G | A | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.202+4616C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084752 | ||||||
| chr22:19084774
|
C | T | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+4594G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084774 | ||||||
| chr22:19084781
|
G | A | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.202+4587C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084781 | ||||||
| chr22:19084788
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.202+4580G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084788 | ||||||
| chr22:19084797
|
C | A | 3 | a0001c0001t0016g0114a0001c0001t0016g0115a0001c0001t0016g0117 | 3 | HG01099.hp1 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.202+4571G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084797 | ||||||
| chr22:19084803
|
G | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.202+4565C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084803 | ||||||
| chr22:19084804
|
G | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+4564C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084804 | ||||||
| chr22:19084808
|
TG | T | 172 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(169): Show | 178 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.202+4559delC | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084808 | ||||||
| chr22:19084823
|
G | A | 6 | a0003c0003t0007g0015a0003c0003t0012g0013a0003c0003t0012g0014others(3): Show | 6 | HG00642.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.202+4545C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084823 | ||||||
| chr22:19084921
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.202+4447C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084921 | ||||||
| chr22:19084969
|
T | C | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.202+4399A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084969 | ||||||
| chr22:19084970
|
G | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.202+4398C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084970 | ||||||
| chr22:19084977
|
T | A | 1 | a0001c0001t0001g0318 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.202+4391A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084977 | ||||||
| chr22:19084991
|
G | C | 4 | a0002c0002t0004g0092a0002c0002t0004g0093a0002c0002t0004g0103others(1): Show | 4 | HG02148.hp1 HG02300.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+4377C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19084991 | ||||||
| chr22:19085096
|
C | T | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.202+4272G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19085096 | ||||||
| chr22:19085105
|
G | GA | 60 | a0001c0001t0051g0319a0002c0002t0002g0006a0002c0002t0002g0133others(57): Show | 63 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.202+4262dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19085105 | ||||||
| chr22:19085105
|
G | GAA | 86 | a0001c0001t0050g0334a0002c0002t0002g0143a0002c0002t0002g0155others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.202+4261_202+4262d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19085105 | ||||||
| chr22:19085106
|
A | G | 2 | a0001c0001t0001g0254a0001c0001t0001g0289 | 2 | HG01517.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.202+4262T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19085106 | ||||||
| chr22:19085276
|
A | G | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.202+4092T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19085276 | ||||||
| chr22:19085383
|
G | C | 22 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(19): Show | 23 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.202+3985C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19085383 | ||||||
| chr22:19085574
|
C | T | 57 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(54): Show | 60 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.202+3794G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19085574 | ||||||
| chr22:19085596
|
G | A | 1 | a0002c0002t0038g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.202+3772C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19085596 | ||||||
| chr22:19086099
|
G | A | 62 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(59): Show | 65 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.202+3269C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086099 | ||||||
| chr22:19086181
|
G | A | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+3187C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086181 | ||||||
| chr22:19086192
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.202+3176C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086192 | ||||||
| chr22:19086242
|
C | G | 1 | a0002c0002t0047g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202+3126G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086242 | ||||||
| chr22:19086250
|
A | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.202+3118T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086250 | ||||||
| chr22:19086252
|
C | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0227 | 2 | NA18950.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.202+3116G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086252 | ||||||
| chr22:19086349
|
G | A | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.202+3019C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086349 | ||||||
| chr22:19086411
|
A | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.202+2957T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086411 | ||||||
| chr22:19086688
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.202+2680C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086688 | ||||||
| chr22:19086879
|
C | T | 2 | a0001c0001t0024g0111a0001c0001t0024g0112 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.202+2489G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086879 | ||||||
| chr22:19086964
|
A | G | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.202+2404T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086964 | ||||||
| chr22:19086987
|
T | C | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.202+2381A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19086987 | ||||||
| chr22:19087081
|
G | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.202+2287C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087081 | ||||||
| chr22:19087131
|
G | C | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.202+2237C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087131 | ||||||
| chr22:19087240
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.202+2128A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087240 | ||||||
| chr22:19087300
|
T | C | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202+2068A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087300 | ||||||
| chr22:19087331
|
G | C | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202+2037C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087331 | ||||||
| chr22:19087360
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.202+2008C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087360 | ||||||
| chr22:19087409
|
A | G | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+1959T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087409 | ||||||
| chr22:19087577
|
G | A | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.202+1791C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087577 | ||||||
| chr22:19087678
|
C | CT | 30 | a0001c0001t0001g0237a0001c0001t0001g0246a0001c0001t0001g0253others(27): Show | 30 | HG00597.hp1 HG01071.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.202+1689dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087678 | ||||||
| chr22:19087678
|
C | CTT | 55 | a0001c0001t0010g0122a0001c0001t0010g0125a0001c0001t0032g0121others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.202+1688_202+1689d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087678 | ||||||
| chr22:19087678
|
CT | C | 35 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(32): Show | 35 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.202+1689delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087678 | ||||||
| chr22:19087857
|
G | T | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.202+1511C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19087857 | ||||||
| chr22:19088051
|
C | T | 1 | a0002c0002t0013g0004 | 2 | HG01496.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.202+1317G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088051 | ||||||
| chr22:19088123
|
T | G | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+1245A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088123 | ||||||
| chr22:19088177
|
C | T | 1 | a0002c0002t0018g0182 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.202+1191G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088177 | ||||||
| chr22:19088443
|
A | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+925T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088443 | ||||||
| chr22:19088481
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+887C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088481 | ||||||
| chr22:19088599
|
G | A | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202+769C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088599 | ||||||
| chr22:19088702
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.202+666G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088702 | ||||||
| chr22:19088766
|
G | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.202+602C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088766 | ||||||
| chr22:19088780
|
T | C | 1 | a0002c0002t0006g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.202+588A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088780 | ||||||
| chr22:19088924
|
G | A | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.202+444C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088924 | ||||||
| chr22:19088962
|
C | T | 2 | a0002c0002t0004g0079a0002c0002t0004g0083 | 2 | NA18940.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.202+406G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19088962 | ||||||
| chr22:19089062
|
C | A | 6 | a0001c0001t0001g0283a0001c0001t0005g0209a0001c0001t0005g0279others(3): Show | 6 | HG01099.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.202+306G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19089062 | ||||||
| chr22:19089087
|
T | C | 1 | a0001c0001t0001g0289 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.202+281A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19089087 | ||||||
| chr22:19089145
|
G | C | 1 | a0002c0002t0009g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.202+223C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19089145 | ||||||
| chr22:19089233
|
G | A | 1 | a0001c0001t0032g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.202+135C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19089233 | ||||||
| chr22:19089284
|
C | A | 42 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(39): Show | 43 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.202+84G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19089284 | ||||||
| chr22:19089322
|
A | G | 4 | a0002c0002t0002g0006a0002c0002t0002g0172a0002c0002t0002g0173others(1): Show | 5 | NA18950.hp1 NA18957.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+46T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 2/9 | chr22 | 19089322 | ||||||
| chr22:19089525
|
G | A | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80-35C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19089525 | ||||||
| chr22:19089536
|
C | T | 302 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0208others(299): Show | 311 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.80-46G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19089536 | ||||||
| chr22:19089563
|
T | A | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-73A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19089563 | ||||||
| chr22:19089576
|
A | ATTTG | 6 | a0002c0002t0003g0003a0002c0002t0003g0070a0002c0002t0003g0072others(3): Show | 7 | HG01243.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-90_80-87dupCAAA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19089576 | ||||||
| chr22:19089674
|
G | A | 3 | a0001c0001t0005g0213a0001c0001t0005g0217a0001c0001t0005g0238 | 3 | HG02280.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.80-184C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19089674 | ||||||
| chr22:19089833
|
G | T | 1 | a0001c0001t0001g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.80-343C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19089833 | ||||||
| chr22:19089932
|
T | C | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-442A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19089932 | ||||||
| chr22:19090081
|
C | T | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.80-591G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090081 | ||||||
| chr22:19090100
|
G | A | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-610C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090100 | ||||||
| chr22:19090111
|
T | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-621A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090111 | ||||||
| chr22:19090214
|
C | T | 4 | a0002c0002t0002g0161a0002c0002t0002g0162a0002c0002t0018g0150others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-724G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090214 | ||||||
| chr22:19090236
|
C | G | 1 | a0001c0001t0001g0303 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.80-746G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090236 | ||||||
| chr22:19090302
|
A | G | 2 | a0001c0001t0005g0220a0001c0001t0005g0245 | 2 | NA18947.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.80-812T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090302 | ||||||
| chr22:19090393
|
C | T | 1 | a0002c0002t0006g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.80-903G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090393 | ||||||
| chr22:19090414
|
C | T | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.80-924G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090414 | ||||||
| chr22:19090544
|
T | A | 2 | a0001c0001t0010g0124a0001c0001t0010g0125 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.80-1054A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090544 | ||||||
| chr22:19090811
|
G | GA | 143 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(140): Show | 150 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.80-1322dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090811 | ||||||
| chr22:19090826
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.80-1336T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090826 | ||||||
| chr22:19090879
|
T | A | 4 | a0001c0001t0010g0123a0001c0001t0010g0124a0001c0001t0010g0125others(1): Show | 4 | HG02970.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1389A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090879 | ||||||
| chr22:19090896
|
C | T | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-1406G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090896 | ||||||
| chr22:19090997
|
A | G | 2 | a0001c0001t0001g0298a0001c0001t0001g0321 | 2 | HG00408.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.80-1507T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19090997 | ||||||
| chr22:19091008
|
A | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-1518T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091008 | ||||||
| chr22:19091024
|
T | TA | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.80-1535dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091024 | ||||||
| chr22:19091046
|
C | A | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.80-1556G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091046 | ||||||
| chr22:19091079
|
A | AG | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.80-1590_80-1589ins others(1): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091079 | ||||||
| chr22:19091094
|
C | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-1604G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091094 | ||||||
| chr22:19091115
|
T | C | 1 | a0002c0002t0011g0329 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.80-1625A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091115 | ||||||
| chr22:19091162
|
C | A | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-1672G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091162 | ||||||
| chr22:19091249
|
C | T | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-1759G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091249 | ||||||
| chr22:19091545
|
G | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-2055C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091545 | ||||||
| chr22:19091615
|
T | C | 2 | a0001c0001t0024g0111a0001c0001t0024g0112 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-2125A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091615 | ||||||
| chr22:19091705
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80-2215T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091705 | ||||||
| chr22:19091728
|
A | G | 62 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(59): Show | 65 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.80-2238T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091728 | ||||||
| chr22:19091812
|
C | T | 1 | a0005c0006t0005g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.80-2322G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091812 | ||||||
| chr22:19091856
|
C | T | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-2366G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091856 | ||||||
| chr22:19091884
|
A | G | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-2394T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091884 | ||||||
| chr22:19091962
|
T | C | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-2472A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091962 | ||||||
| chr22:19091966
|
G | C | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-2476C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19091966 | ||||||
| chr22:19092047
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.80-2557A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092047 | ||||||
| chr22:19092094
|
T | A | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-2604A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092094 | ||||||
| chr22:19092095
|
C | A | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-2605G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092095 | ||||||
| chr22:19092205
|
G | A | 1 | a0002c0002t0038g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.80-2715C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092205 | ||||||
| chr22:19092287
|
G | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-2797C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092287 | ||||||
| chr22:19092322
|
C | T | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-2832G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092322 | ||||||
| chr22:19092343
|
T | TA | 141 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(138): Show | 148 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.80-2854dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092343 | ||||||
| chr22:19092356
|
A | AC | 6 | a0002c0002t0017g0146a0002c0002t0017g0160a0002c0002t0017g0178others(3): Show | 6 | HG01515.hp2 HG01517.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-2867_80-2866ins others(1): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092356 | ||||||
| chr22:19092403
|
G | C | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-2913C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092403 | ||||||
| chr22:19092637
|
A | G | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-3147T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092637 | ||||||
| chr22:19092743
|
C | T | 3 | a0001c0001t0005g0213a0001c0001t0005g0217a0001c0001t0005g0238 | 3 | HG02280.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.80-3253G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092743 | ||||||
| chr22:19092787
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-3297A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092787 | ||||||
| chr22:19092897
|
AGAG | A | 176 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(173): Show | 183 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.80-3410_80-3408del others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092897 | ||||||
| chr22:19092988
|
AAGAAG | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-3503_80-3499del others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092988 | ||||||
| chr22:19092999
|
A | G | 5 | a0001c0001t0001g0253a0002c0002t0017g0146a0002c0002t0017g0160others(2): Show | 5 | HG03239.hp1 NA18945.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-3509T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19092999 | ||||||
| chr22:19093027
|
C | G | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-3537G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093027 | ||||||
| chr22:19093092
|
G | A | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-3602C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093092 | ||||||
| chr22:19093159
|
C | T | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-3669G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093159 | ||||||
| chr22:19093161
|
A | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-3671T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093161 | ||||||
| chr22:19093361
|
GA | G | 155 | a0001c0001t0001g0219a0001c0001t0010g0113a0001c0001t0010g0118others(152): Show | 162 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.80-3872delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093361 | ||||||
| chr22:19093386
|
C | A | 173 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(170): Show | 180 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.80-3896G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093386 | ||||||
| chr22:19093429
|
G | A | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-3939C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093429 | ||||||
| chr22:19093461
|
C | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-3971G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093461 | ||||||
| chr22:19093620
|
AT | A | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-4131delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093620 | ||||||
| chr22:19093726
|
A | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-4236T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093726 | ||||||
| chr22:19093749
|
C | G | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-4259G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093749 | ||||||
| chr22:19093842
|
A | C | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0005g0262others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-4352T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19093842 | ||||||
| chr22:19094007
|
T | TA | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-4518dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094007 | ||||||
| chr22:19094017
|
TAATA | T | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-4531_80-4528del others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094017 | ||||||
| chr22:19094071
|
T | C | 1 | a0002c0002t0009g0104 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.80-4581A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094071 | ||||||
| chr22:19094198
|
T | G | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-4708A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094198 | ||||||
| chr22:19094282
|
G | T | 8 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(5): Show | 8 | HG00597.hp1 HG00621.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-4792C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094282 | ||||||
| chr22:19094290
|
C | T | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-4800G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094290 | ||||||
| chr22:19094291
|
G | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.80-4801C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094291 | ||||||
| chr22:19094297
|
G | A | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-4807C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094297 | ||||||
| chr22:19094317
|
A | C | 1 | a0001c0001t0024g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.80-4827T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094317 | ||||||
| chr22:19094380
|
G | A | 1 | a0002c0002t0038g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.80-4890C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094380 | ||||||
| chr22:19094390
|
ACTCCAGT others(1229): Show |
A | 1 | a0001c0001t0001g0265 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.80-6136_80-4901del | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094390 | ||||||
| chr22:19094403
|
C | T | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-4913G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094403 | ||||||
| chr22:19094404
|
G | A | 24 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(21): Show | 25 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.80-4914C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094404 | ||||||
| chr22:19094423
|
TCAA | T | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-4936_80-4934del others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094423 | ||||||
| chr22:19094494
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0230 | 2 | HG00323.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-5004T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094494 | ||||||
| chr22:19094721
|
G | C | 1 | a0001c0004t0015g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.80-5231C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094721 | ||||||
| chr22:19094754
|
T | C | 1 | a0003c0003t0028g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.80-5264A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094754 | ||||||
| chr22:19094833
|
T | C | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.80-5343A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094833 | ||||||
| chr22:19094838
|
G | A | 2 | a0002c0002t0003g0072a0002c0002t0003g0073 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.80-5348C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094838 | ||||||
| chr22:19094989
|
G | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-5499C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19094989 | ||||||
| chr22:19095013
|
C | T | 2 | a0001c0001t0024g0111a0001c0001t0024g0112 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.80-5523G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095013 | ||||||
| chr22:19095022
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-5532A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095022 | ||||||
| chr22:19095223
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-5733C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095223 | ||||||
| chr22:19095264
|
A | G | 1 | a0006c0007t0001g0281 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.80-5774T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095264 | ||||||
| chr22:19095443
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-5953A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095443 | ||||||
| chr22:19095478
|
G | A | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-5988C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095478 | ||||||
| chr22:19095578
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.80-6088C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095578 | ||||||
| chr22:19095594
|
G | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-6104C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095594 | ||||||
| chr22:19095639
|
C | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-6149G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095639 | ||||||
| chr22:19095640
|
A | G | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.80-6150T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095640 | ||||||
| chr22:19095660
|
C | CA | 18 | a0001c0001t0001g0273a0001c0001t0001g0294a0001c0001t0001g0302others(15): Show | 18 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.80-6171dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095660 | ||||||
| chr22:19095677
|
AC | A | 7 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(4): Show | 7 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-6188delG | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095677 | ||||||
| chr22:19095678
|
C | A | 4 | a0001c0001t0010g0123a0001c0001t0010g0124a0001c0001t0010g0125others(1): Show | 4 | HG02970.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-6188G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095678 | ||||||
| chr22:19095737
|
C | CTTT | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-6250_80-6248dup others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095737 | ||||||
| chr22:19095737
|
C | CTTTT | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-6251_80-6248dup others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19095737 | ||||||
| chr22:19096039
|
A | T | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.80-6549T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096039 | ||||||
| chr22:19096041
|
C | T | 1 | a0002c0002t0003g0050 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.80-6551G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096041 | ||||||
| chr22:19096044
|
T | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-6554A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096044 | ||||||
| chr22:19096109
|
C | T | 1 | a0002c0002t0003g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.80-6619G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096109 | ||||||
| chr22:19096131
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.80-6641G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096131 | ||||||
| chr22:19096165
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-6675A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096165 | ||||||
| chr22:19096174
|
CTTA | C | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-6687_80-6685del others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096174 | ||||||
| chr22:19096469
|
CAAGAA | C | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.80-6984_80-6980del others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096469 | ||||||
| chr22:19096523
|
T | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-7033A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096523 | ||||||
| chr22:19096562
|
A | AC | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-7073dupG | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096562 | ||||||
| chr22:19096597
|
A | C | 24 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(21): Show | 25 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.80-7107T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096597 | ||||||
| chr22:19096597
|
AC | A | 12 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(9): Show | 12 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-7108delG | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096597 | ||||||
| chr22:19096598
|
C | A | 184 | a0001c0001t0030g0116a0001c0001t0050g0334a0001c0004t0015g0128others(181): Show | 191 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.80-7108G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096598 | ||||||
| chr22:19096604
|
A | T | 147 | a0001c0001t0005g0279a0001c0001t0050g0334a0002c0002t0002g0006others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-7114T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096604 | ||||||
| chr22:19096605
|
T | A | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-7115A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096605 | ||||||
| chr22:19096624
|
AG | A | 273 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(270): Show | 279 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.80-7135delC | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096624 | ||||||
| chr22:19096626
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-7136C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096626 | ||||||
| chr22:19096632
|
G | A | 273 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(270): Show | 279 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.80-7142C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096632 | ||||||
| chr22:19096633
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-7143C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096633 | ||||||
| chr22:19096818
|
C | T | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-7328G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096818 | ||||||
| chr22:19096894
|
C | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-7404G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096894 | ||||||
| chr22:19096894
|
C | CA | 12 | a0001c0001t0001g0222a0001c0001t0001g0323a0001c0001t0010g0113others(9): Show | 12 | HG02451.hp1 HG02809.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-7405dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096894 | ||||||
| chr22:19096894
|
CA | C | 69 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(66): Show | 72 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.80-7405delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096894 | ||||||
| chr22:19096895
|
A | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-7405T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096895 | ||||||
| chr22:19096898
|
A | C | 47 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(44): Show | 50 | HG00323.hp2 HG00408.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.80-7408T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096898 | ||||||
| chr22:19096914
|
T | C | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-7424A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19096914 | ||||||
| chr22:19097042
|
A | G | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-7552T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097042 | ||||||
| chr22:19097176
|
G | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-7686C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097176 | ||||||
| chr22:19097252
|
T | C | 1 | a0002c0002t0004g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.80-7762A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097252 | ||||||
| chr22:19097260
|
T | C | 1 | a0002c0002t0004g0096 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.80-7770A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097260 | ||||||
| chr22:19097327
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-7837C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097327 | ||||||
| chr22:19097484
|
G | A | 1 | a0003c0003t0007g0028 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.80-7994C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097484 | ||||||
| chr22:19097588
|
T | C | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-8098A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097588 | ||||||
| chr22:19097689
|
T | C | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-8199A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097689 | ||||||
| chr22:19097896
|
C | G | 38 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(35): Show | 38 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.80-8406G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19097896 | ||||||
| chr22:19098021
|
A | C | 2 | a0002c0002t0006g0179a0002c0002t0006g0181 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80-8531T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098021 | ||||||
| chr22:19098025
|
C | T | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-8535G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098025 | ||||||
| chr22:19098032
|
A | G | 3 | a0003c0003t0007g0020a0003c0003t0007g0033a0003c0003t0007g0036 | 3 | NA19004.hp1 NA19009.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.80-8542T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098032 | ||||||
| chr22:19098083
|
T | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-8593A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098083 | ||||||
| chr22:19098093
|
A | T | 1 | a0001c0004t0023g0127 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-8603T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098093 | ||||||
| chr22:19098094
|
T | A | 1 | a0001c0004t0023g0127 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-8604A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098094 | ||||||
| chr22:19098094
|
T | TA | 6 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(3): Show | 6 | HG01071.hp2 HG01168.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-8605dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098094 | ||||||
| chr22:19098283
|
G | GTT | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.80-8795_80-8794dup others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098283 | ||||||
| chr22:19098288
|
C | T | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.80-8798G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098288 | ||||||
| chr22:19098289
|
C | T | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.80-8799G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098289 | ||||||
| chr22:19098467
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.80-8977G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098467 | ||||||
| chr22:19098507
|
A | C | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-9017T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098507 | ||||||
| chr22:19098582
|
ATACATGT others(11): Show |
A | 1 | a0001c0001t0001g0294 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.80-9110_80-9093del others(18): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098582 | ||||||
| chr22:19098670
|
G | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-9180C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098670 | ||||||
| chr22:19098786
|
G | C | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-9296C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19098786 | ||||||
| chr22:19099007
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-9517A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099007 | ||||||
| chr22:19099167
|
C | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-9677G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099167 | ||||||
| chr22:19099212
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.80-9722A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099212 | ||||||
| chr22:19099217
|
T | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.80-9727A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099217 | ||||||
| chr22:19099255
|
A | G | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-9765T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099255 | ||||||
| chr22:19099311
|
G | A | 1 | a0001c0001t0005g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.80-9821C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099311 | ||||||
| chr22:19099391
|
C | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.80-9901G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099391 | ||||||
| chr22:19099441
|
T | C | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80-9951A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099441 | ||||||
| chr22:19099554
|
A | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-10064T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099554 | ||||||
| chr22:19099697
|
G | A | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-10207C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099697 | ||||||
| chr22:19099708
|
C | T | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80-10218G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099708 | ||||||
| chr22:19099727
|
T | C | 1 | a0003c0003t0012g0018 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.80-10237A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099727 | ||||||
| chr22:19099739
|
G | A | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-10249C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099739 | ||||||
| chr22:19099744
|
G | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-10254C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099744 | ||||||
| chr22:19099854
|
C | T | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-10364G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099854 | ||||||
| chr22:19099948
|
C | T | 1 | a0001c0001t0005g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-10458G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099948 | ||||||
| chr22:19099970
|
T | TA | 162 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(159): Show | 169 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.80-10481dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099970 | ||||||
| chr22:19099970
|
T | TAA | 33 | a0002c0002t0002g0151a0002c0002t0002g0159a0002c0002t0002g0170others(30): Show | 33 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-10482_80-10481d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19099970 | ||||||
| chr22:19100391
|
C | T | 1 | a0002c0002t0006g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80-10901G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100391 | ||||||
| chr22:19100402
|
T | G | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-10912A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100402 | ||||||
| chr22:19100426
|
C | T | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-10936G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100426 | ||||||
| chr22:19100428
|
C | T | 1 | a0002c0002t0009g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.80-10938G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100428 | ||||||
| chr22:19100492
|
C | T | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.80-11002G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100492 | ||||||
| chr22:19100558
|
C | A | 2 | a0001c0004t0023g0127a0001c0004t0023g0132 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.80-11068G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100558 | ||||||
| chr22:19100664
|
T | TA | 202 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0208others(199): Show | 207 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.80-11175dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100664 | ||||||
| chr22:19100664
|
T | TAA | 19 | a0001c0001t0001g0282a0001c0001t0001g0309a0001c0001t0010g0113others(16): Show | 19 | HG01952.hp1 HG02148.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-11176_80-11175d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100664 | ||||||
| chr22:19100725
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.80-11235A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100725 | ||||||
| chr22:19100861
|
T | C | 6 | a0002c0002t0002g0134a0002c0002t0002g0156a0002c0002t0002g0163others(3): Show | 6 | HG00408.hp2 NA18747.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-11371A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100861 | ||||||
| chr22:19100963
|
G | A | 5 | a0001c0001t0001g0250a0001c0001t0001g0258a0001c0001t0001g0259others(2): Show | 5 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-11473C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100963 | ||||||
| chr22:19100977
|
G | A | 3 | a0003c0003t0007g0020a0003c0003t0007g0033a0003c0003t0007g0036 | 3 | NA19004.hp1 NA19009.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.80-11487C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19100977 | ||||||
| chr22:19101036
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.80-11546C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101036 | ||||||
| chr22:19101069
|
C | T | 2 | a0002c0002t0003g0050a0002c0002t0003g0067 | 2 | HG02155.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.80-11579G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101069 | ||||||
| chr22:19101094
|
C | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.80-11604G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101094 | ||||||
| chr22:19101171
|
A | C | 2 | a0002c0002t0033g0107a0002c0002t0039g0110 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80-11681T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101171 | ||||||
| chr22:19101181
|
T | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-11691A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101181 | ||||||
| chr22:19101400
|
G | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.80-11910C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101400 | ||||||
| chr22:19101446
|
AAAGT | A | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-11960_80-11957d others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101446 | ||||||
| chr22:19101507
|
G | A | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-12017C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101507 | ||||||
| chr22:19101601
|
C | T | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-12111G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101601 | ||||||
| chr22:19101609
|
C | T | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-12119G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101609 | ||||||
| chr22:19101638
|
G | C | 6 | a0002c0002t0004g0090a0002c0002t0004g0091a0002c0002t0004g0097others(3): Show | 6 | HG00438.hp1 NA18947.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-12148C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101638 | ||||||
| chr22:19101674
|
G | A | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-12184C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101674 | ||||||
| chr22:19101737
|
T | TA | 7 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0234others(4): Show | 7 | HG00323.hp1 HG00323.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-12248dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101737 | ||||||
| chr22:19101737
|
T | TAA | 77 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(74): Show | 78 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.80-12249_80-12248d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101737 | ||||||
| chr22:19101737
|
T | TAAA | 93 | a0001c0001t0050g0334a0002c0002t0002g0157a0002c0002t0003g0002others(90): Show | 99 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.80-12250_80-12248d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19101737 | ||||||
| chr22:19102080
|
C | T | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-12590G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102080 | ||||||
| chr22:19102182
|
T | C | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-12692A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102182 | ||||||
| chr22:19102201
|
T | C | 1 | a0002c0002t0002g0165 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.80-12711A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102201 | ||||||
| chr22:19102244
|
G | A | 8 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(5): Show | 8 | HG00597.hp1 HG00621.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-12754C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102244 | ||||||
| chr22:19102494
|
C | T | 6 | a0001c0001t0005g0213a0001c0001t0005g0217a0001c0001t0005g0238others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-13004G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102494 | ||||||
| chr22:19102557
|
C | T | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-13067G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102557 | ||||||
| chr22:19102635
|
G | A | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-13145C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102635 | ||||||
| chr22:19102689
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.80-13199C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102689 | ||||||
| chr22:19102701
|
C | CA | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-13212dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102701 | ||||||
| chr22:19102736
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-13246A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102736 | ||||||
| chr22:19102737
|
G | A | 2 | a0002c0002t0018g0150a0002c0002t0018g0158 | 2 | HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.80-13247C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102737 | ||||||
| chr22:19102754
|
G | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-13264C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102754 | ||||||
| chr22:19102851
|
GA | G | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-13362delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102851 | ||||||
| chr22:19102857
|
T | G | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-13367A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19102857 | ||||||
| chr22:19103284
|
T | TA | 65 | a0001c0001t0001g0272a0001c0001t0005g0213a0002c0002t0002g0006others(62): Show | 68 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.80-13795dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103284 | ||||||
| chr22:19103406
|
A | T | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-13916T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103406 | ||||||
| chr22:19103408
|
A | G | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-13918T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103408 | ||||||
| chr22:19103416
|
C | CT | 30 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0203others(27): Show | 30 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-13927dupA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
C | CTT | 10 | a0001c0001t0001g0197a0001c0001t0001g0202a0001c0001t0001g0237others(7): Show | 10 | HG01175.hp1 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-13928_80-13927d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
C | CTTT | 6 | a0001c0001t0001g0264a0001c0001t0001g0272a0001c0001t0001g0301others(3): Show | 6 | HG01168.hp1 HG03225.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-13929_80-13927d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CT | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(31): Show | 36 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.80-13927delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTT | C | 29 | a0001c0001t0010g0118a0002c0002t0002g0006a0002c0002t0002g0133others(26): Show | 32 | HG00408.hp2 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.80-13928_80-13927d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTT | C | 28 | a0001c0001t0010g0113a0001c0001t0010g0119a0002c0002t0002g0141others(25): Show | 28 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.80-13929_80-13927d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTT | C | 10 | a0003c0003t0007g0028a0003c0003t0008g0010a0003c0003t0008g0021others(7): Show | 10 | HG00642.hp1 HG02056.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-13930_80-13927d others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTTT | C | 17 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0026others(14): Show | 17 | HG01256.hp2 HG01258.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-13931_80-13927d others(7): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-13937_80-13927d others(13): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0050g0334a0002c0005t0020g0191a0002c0005t0043g0138others(2): Show | 5 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-13938_80-13927d others(14): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTTTTT others(6): Show |
C | 26 | a0002c0002t0003g0003a0002c0002t0003g0068a0002c0002t0003g0070others(23): Show | 27 | HG00438.hp1 HG01243.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.80-13939_80-13927d others(15): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTTTTT others(7): Show |
C | 36 | a0002c0002t0004g0076a0002c0002t0004g0078a0002c0002t0004g0079others(33): Show | 38 | HG00544.hp1 HG00673.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.80-13940_80-13927d others(16): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-13941_80-13927d others(17): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80-13943_80-13927d others(19): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103416
|
CTTTTTTT others(11): Show |
C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-13944_80-13927d others(20): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103416 | ||||||
| chr22:19103455
|
G | A | 1 | a0001c0001t0010g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.80-13965C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103455 | ||||||
| chr22:19103573
|
C | T | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.80-14083G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103573 | ||||||
| chr22:19103583
|
C | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0272a0001c0001t0001g0273others(24): Show | 28 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-14093G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103583 | ||||||
| chr22:19103680
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG01175.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-14190C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103680 | ||||||
| chr22:19103739
|
T | TA | 16 | a0001c0001t0001g0237a0001c0001t0001g0272a0001c0001t0001g0294others(13): Show | 16 | HG00621.hp1 HG01169.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-14250dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103739 | ||||||
| chr22:19103739
|
T | TAA | 72 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(69): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.80-14251_80-14250d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103739 | ||||||
| chr22:19103739
|
T | TAAA | 8 | a0002c0002t0002g0167a0002c0002t0002g0168a0002c0002t0002g0173others(5): Show | 8 | HG01952.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-14252_80-14250d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103739 | ||||||
| chr22:19103739
|
TA | T | 40 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0227others(37): Show | 40 | HG00642.hp1 HG01070.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.80-14250delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103739 | ||||||
| chr22:19103764
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0244 | 2 | NA18995.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.80-14274C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103764 | ||||||
| chr22:19103772
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80-14282C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19103772 | ||||||
| chr22:19104027
|
AAG | A | 12 | a0002c0002t0009g0005a0002c0002t0009g0074a0002c0002t0009g0084others(9): Show | 13 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-14539_80-14538d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104027 | ||||||
| chr22:19104267
|
T | C | 1 | a0001c0004t0015g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.80-14777A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104267 | ||||||
| chr22:19104383
|
AG | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-14894delC | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104383 | ||||||
| chr22:19104383
|
AGG | A | 135 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(132): Show | 139 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.80-14895_80-14894d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104383 | ||||||
| chr22:19104385
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-14895C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104385 | ||||||
| chr22:19104386
|
C | A | 135 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(132): Show | 139 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.80-14896G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104386 | ||||||
| chr22:19104386
|
C | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-14896G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104386 | ||||||
| chr22:19104388
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-14898C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104388 | ||||||
| chr22:19104388
|
G | T | 135 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(132): Show | 139 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.80-14898C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104388 | ||||||
| chr22:19104389
|
T | A | 135 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(132): Show | 139 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.80-14899A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104389 | ||||||
| chr22:19104390
|
C | G | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-14900G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104390 | ||||||
| chr22:19104391
|
T | G | 135 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(132): Show | 139 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.80-14901A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104391 | ||||||
| chr22:19104391
|
TC | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-14902delG | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104391 | ||||||
| chr22:19104392
|
C | T | 135 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(132): Show | 139 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.80-14902G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104392 | ||||||
| chr22:19104464
|
C | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-14974G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104464 | ||||||
| chr22:19104709
|
C | G | 92 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(89): Show | 96 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.80-15219G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104709 | ||||||
| chr22:19104903
|
GAGA | G | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-15416_80-15414d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19104903 | ||||||
| chr22:19105016
|
C | T | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-15526G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105016 | ||||||
| chr22:19105050
|
C | T | 1 | a0003c0003t0008g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.80-15560G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105050 | ||||||
| chr22:19105093
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.80-15603G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105093 | ||||||
| chr22:19105106
|
G | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-15616C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105106 | ||||||
| chr22:19105126
|
C | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-15636G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105126 | ||||||
| chr22:19105160
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0016g0044 | 2 | HG01175.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.80-15670A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105160 | ||||||
| chr22:19105192
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.80-15702C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105192 | ||||||
| chr22:19105218
|
G | A | 1 | a0002c0002t0006g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80-15728C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105218 | ||||||
| chr22:19105289
|
A | ACTCCAGC others(5): Show |
1 | a0001c0001t0052g0335 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.80-15811_80-15800d others(14): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105289 | ||||||
| chr22:19105401
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.80-15911C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105401 | ||||||
| chr22:19105520
|
T | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.80-16030A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105520 | ||||||
| chr22:19105534
|
T | C | 185 | a0001c0001t0030g0116a0001c0001t0050g0334a0001c0004t0015g0128others(182): Show | 192 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.80-16044A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105534 | ||||||
| chr22:19105571
|
C | T | 1 | a0002c0002t0002g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.80-16081G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105571 | ||||||
| chr22:19105572
|
A | G | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.80-16082T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105572 | ||||||
| chr22:19105645
|
A | G | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-16155T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105645 | ||||||
| chr22:19105668
|
T | C | 3 | a0003c0003t0007g0028a0003c0003t0008g0030a0003c0003t0012g0029 | 3 | NA18981.hp1 NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.80-16178A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105668 | ||||||
| chr22:19105706
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.80-16216C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105706 | ||||||
| chr22:19105710
|
G | GC | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0192others(331): Show | 343 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.80-16221_80-16220i others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105710 | ||||||
| chr22:19105785
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.80-16295T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105785 | ||||||
| chr22:19105872
|
A | G | 1 | a0001c0001t0005g0262 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.79+16256T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105872 | ||||||
| chr22:19105926
|
G | A | 21 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(18): Show | 22 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+16202C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19105926 | ||||||
| chr22:19106106
|
G | A | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+16022C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19106106 | ||||||
| chr22:19106361
|
G | A | 8 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+15767C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19106361 | ||||||
| chr22:19106401
|
C | T | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+15727G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19106401 | ||||||
| chr22:19106652
|
C | T | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.79+15476G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19106652 | ||||||
| chr22:19106708
|
G | A | 2 | a0002c0002t0011g0330a0002c0002t0046g0324 | 2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+15420C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19106708 | ||||||
| chr22:19106814
|
A | T | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.79+15314T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19106814 | ||||||
| chr22:19106913
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.79+15215G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19106913 | ||||||
| chr22:19106950
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.79+15178A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19106950 | ||||||
| chr22:19107170
|
G | A | 1 | a0002c0002t0002g0169 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.79+14958C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19107170 | ||||||
| chr22:19107758
|
T | C | 1 | a0002c0002t0006g0181 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.79+14370A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19107758 | ||||||
| chr22:19107922
|
T | C | 3 | a0002c0002t0003g0058a0002c0002t0003g0059a0002c0002t0034g0047 | 3 | NA18951.hp2 NA18957.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.79+14206A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19107922 | ||||||
| chr22:19108108
|
G | A | 1 | a0002c0002t0011g0330 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79+14020C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108108 | ||||||
| chr22:19108113
|
C | A | 1 | a0002c0002t0004g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+14015G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108113 | ||||||
| chr22:19108151
|
A | T | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.79+13977T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108151 | ||||||
| chr22:19108175
|
G | A | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.79+13953C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108175 | ||||||
| chr22:19108318
|
C | A | 1 | a0002c0002t0003g0048 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.79+13810G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108318 | ||||||
| chr22:19108520
|
A | G | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+13608T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108520 | ||||||
| chr22:19108569
|
T | TA | 12 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(9): Show | 12 | HG00639.hp1 HG01175.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+13558dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0010g0125 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.79+13549_79+13558d others(12): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
T | TAAAAAAA others(13): Show |
1 | a0001c0001t0010g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79+13539_79+13558d others(22): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TA | T | 12 | a0001c0001t0001g0194a0001c0001t0001g0207a0001c0001t0001g0240others(9): Show | 12 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+13558delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAA | T | 34 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(31): Show | 34 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.79+13557_79+13558d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAA | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0208a0001c0001t0001g0212others(47): Show | 51 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.79+13556_79+13558d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAAAAAA others(1): Show |
T | 6 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+13551_79+13558d others(10): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAAAAAA others(3): Show |
T | 4 | a0003c0003t0008g0031a0003c0003t0008g0032a0003c0003t0012g0016others(1): Show | 4 | HG01975.hp2 HG03688.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+13549_79+13558d others(12): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAAAAAA others(4): Show |
T | 26 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(23): Show | 26 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+13548_79+13558d others(13): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0001g0250 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.79+13545_79+13558d others(16): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAAAAAA others(11): Show |
T | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+13541_79+13558d others(20): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAAAAAA others(13): Show |
T | 46 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(43): Show | 47 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.79+13539_79+13558d others(22): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAAAAAA others(14): Show |
T | 105 | a0001c0001t0001g0007a0001c0001t0001g0246a0001c0001t0001g0247others(102): Show | 112 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.79+13538_79+13558d others(23): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108569
|
TAAAAAAA others(15): Show |
T | 1 | a0002c0002t0014g0042 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.79+13537_79+13558d others(24): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108569 | ||||||
| chr22:19108649
|
T | C | 1 | a0002c0002t0009g0005 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.79+13479A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108649 | ||||||
| chr22:19108669
|
C | T | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+13459G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108669 | ||||||
| chr22:19108844
|
A | C | 3 | a0001c0001t0010g0123a0001c0001t0010g0124a0001c0001t0010g0125 | 3 | HG02970.hp2 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.79+13284T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108844 | ||||||
| chr22:19108858
|
C | CA | 11 | a0001c0001t0001g0282a0001c0001t0005g0245a0001c0001t0010g0113others(8): Show | 11 | HG00738.hp2 HG02148.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+13269dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108858 | ||||||
| chr22:19108858
|
CA | C | 24 | a0001c0001t0001g0274a0001c0001t0010g0120a0002c0002t0003g0002others(21): Show | 25 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.79+13269delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108858 | ||||||
| chr22:19108890
|
G | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+13238C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19108890 | ||||||
| chr22:19109018
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+13110C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109018 | ||||||
| chr22:19109061
|
A | G | 1 | a0001c0001t0005g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+13067T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109061 | ||||||
| chr22:19109093
|
C | A | 1 | a0001c0001t0052g0335 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.79+13035G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109093 | ||||||
| chr22:19109114
|
T | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+13014A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109114 | ||||||
| chr22:19109160
|
T | C | 22 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(19): Show | 23 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.79+12968A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109160 | ||||||
| chr22:19109182
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.79+12946G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109182 | ||||||
| chr22:19109315
|
T | C | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.79+12813A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109315 | ||||||
| chr22:19109560
|
T | C | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+12568A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109560 | ||||||
| chr22:19109624
|
T | G | 1 | a0001c0001t0001g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.79+12504A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109624 | ||||||
| chr22:19109706
|
A | C | 1 | a0002c0002t0002g0183 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.79+12422T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109706 | ||||||
| chr22:19109809
|
G | A | 4 | a0002c0002t0009g0005a0002c0002t0009g0104a0002c0002t0009g0105others(1): Show | 5 | HG01257.hp2 HG01258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+12319C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109809 | ||||||
| chr22:19109811
|
A | T | 1 | a0002c0002t0003g0048 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.79+12317T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109811 | ||||||
| chr22:19109814
|
C | T | 6 | a0002c0002t0003g0003a0002c0002t0003g0070a0002c0002t0003g0072others(3): Show | 7 | HG01243.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+12314G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109814 | ||||||
| chr22:19109870
|
A | T | 1 | a0001c0001t0005g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.79+12258T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109870 | ||||||
| chr22:19109924
|
G | A | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.79+12204C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19109924 | ||||||
| chr22:19110042
|
C | G | 1 | a0001c0001t0010g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79+12086G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110042 | ||||||
| chr22:19110118
|
T | C | 3 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0051g0319 | 3 | HG02080.hp1 NA18965.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.79+12010A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110118 | ||||||
| chr22:19110167
|
G | C | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.79+11961C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110167 | ||||||
| chr22:19110187
|
C | T | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+11941G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110187 | ||||||
| chr22:19110324
|
T | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0246a0001c0001t0001g0247others(25): Show | 29 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+11804A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110324 | ||||||
| chr22:19110326
|
C | T | 62 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(59): Show | 65 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.79+11802G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110326 | ||||||
| chr22:19110465
|
T | C | 1 | a0001c0001t0024g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.79+11663A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110465 | ||||||
| chr22:19110507
|
A | G | 1 | a0003c0003t0012g0013 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.79+11621T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110507 | ||||||
| chr22:19110590
|
T | A | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+11538A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110590 | ||||||
| chr22:19110636
|
T | TA | 173 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(170): Show | 178 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.79+11491dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110636 | ||||||
| chr22:19110637
|
A | T | 6 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(3): Show | 6 | HG01346.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+11491T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110637 | ||||||
| chr22:19110716
|
A | G | 55 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(52): Show | 58 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.79+11412T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110716 | ||||||
| chr22:19110727
|
A | G | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+11401T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110727 | ||||||
| chr22:19110746
|
T | G | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.79+11382A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110746 | ||||||
| chr22:19110987
|
T | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+11141A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19110987 | ||||||
| chr22:19111009
|
T | C | 10 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(7): Show | 10 | HG02451.hp1 HG02630.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+11119A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111009 | ||||||
| chr22:19111015
|
T | C | 1 | a0002c0002t0018g0140 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.79+11113A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111015 | ||||||
| chr22:19111129
|
G | A | 196 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(193): Show | 203 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.79+10999C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111129 | ||||||
| chr22:19111453
|
T | C | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+10675A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111453 | ||||||
| chr22:19111609
|
A | G | 2 | a0002c0005t0020g0135a0002c0005t0020g0136 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.79+10519T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111609 | ||||||
| chr22:19111677
|
T | C | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.79+10451A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111677 | ||||||
| chr22:19111690
|
C | A | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+10438G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111690 | ||||||
| chr22:19111705
|
G | A | 1 | a0002c0005t0045g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+10423C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111705 | ||||||
| chr22:19111767
|
C | G | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+10361G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111767 | ||||||
| chr22:19111801
|
T | C | 22 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(19): Show | 23 | HG01243.hp1 HG01255.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+10327A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111801 | ||||||
| chr22:19111845
|
AT | A | 8 | a0002c0002t0003g0003a0002c0002t0003g0070a0002c0002t0003g0072others(5): Show | 9 | HG01243.hp1 HG01346.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+10282delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111845 | ||||||
| chr22:19111847
|
TTTTTA | T | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+10276_79+10280d others(7): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111847 | ||||||
| chr22:19111848
|
TTTTA | T | 52 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(49): Show | 55 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.79+10276_79+10279d others(6): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111848 | ||||||
| chr22:19111849
|
TTTA | T | 53 | a0001c0001t0050g0334a0002c0002t0002g0175a0002c0002t0002g0190others(50): Show | 55 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.79+10276_79+10278d others(5): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111849 | ||||||
| chr22:19111849
|
TTTATTTA others(4): Show |
T | 2 | a0002c0002t0025g0145a0002c0002t0025g0171 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.79+10268_79+10278d others(13): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111849 | ||||||
| chr22:19111854
|
TTA | T | 7 | a0002c0002t0003g0003a0002c0002t0003g0070a0002c0002t0003g0072others(4): Show | 8 | HG01243.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+10272_79+10273d others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111854 | ||||||
| chr22:19111855
|
TA | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+10272delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111855 | ||||||
| chr22:19111856
|
A | T | 108 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(105): Show | 113 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.79+10272T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111856 | ||||||
| chr22:19111860
|
A | T | 151 | a0001c0001t0050g0334a0001c0004t0015g0128a0001c0004t0015g0129others(148): Show | 158 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.79+10268T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111860 | ||||||
| chr22:19111906
|
A | G | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+10222T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19111906 | ||||||
| chr22:19112039
|
C | G | 154 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(151): Show | 160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.79+10089G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112039 | ||||||
| chr22:19112134
|
G | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+9994C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112134 | ||||||
| chr22:19112170
|
G | A | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.79+9958C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112170 | ||||||
| chr22:19112207
|
A | G | 31 | a0001c0001t0030g0116a0001c0004t0015g0128a0001c0004t0015g0129others(28): Show | 32 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.79+9921T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112207 | ||||||
| chr22:19112222
|
G | GAGGTCGC others(18): Show |
1 | a0002c0002t0038g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.79+9881_79+9905dup others(25): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112222 | ||||||
| chr22:19112270
|
CT | C | 4 | a0002c0002t0014g0039a0002c0002t0014g0040a0002c0002t0014g0041others(1): Show | 4 | NA18942.hp1 NA18978.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+9857delA | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112270 | ||||||
| chr22:19112274
|
T | TA | 40 | a0001c0001t0001g0263a0001c0001t0001g0270a0001c0001t0001g0278others(37): Show | 41 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.79+9853dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112274 | ||||||
| chr22:19112274
|
TA | T | 149 | a0001c0001t0001g0272a0001c0001t0005g0210a0001c0001t0005g0211others(146): Show | 155 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.79+9853delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112274 | ||||||
| chr22:19112276
|
A | T | 1 | a0002c0002t0004g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.79+9852T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112276 | ||||||
| chr22:19112300
|
A | C | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+9828T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112300 | ||||||
| chr22:19112301
|
A | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+9827T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112301 | ||||||
| chr22:19112304
|
A | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+9824T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112304 | ||||||
| chr22:19112307
|
A | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+9821T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112307 | ||||||
| chr22:19112417
|
ATGGTTTC others(688): Show |
A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+9016_79+9710del | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112417 | ||||||
| chr22:19112867
|
T | A | 63 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(60): Show | 66 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.79+9261A>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112867 | ||||||
| chr22:19112891
|
T | C | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+9237A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19112891 | ||||||
| chr22:19113034
|
A | G | 63 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(60): Show | 66 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.79+9094T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113034 | ||||||
| chr22:19113074
|
C | T | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+9054G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113074 | ||||||
| chr22:19113168
|
G | A | 4 | a0002c0002t0014g0039a0002c0002t0014g0040a0002c0002t0014g0041others(1): Show | 4 | NA18942.hp1 NA18978.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+8960C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113168 | ||||||
| chr22:19113222
|
T | G | 1 | a0001c0001t0001g0310 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.79+8906A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113222 | ||||||
| chr22:19113230
|
T | C | 199 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(196): Show | 206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.79+8898A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113230 | ||||||
| chr22:19113238
|
C | T | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+8890G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113238 | ||||||
| chr22:19113264
|
G | A | 63 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(60): Show | 66 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.79+8864C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113264 | ||||||
| chr22:19113364
|
G | A | 1 | a0001c0001t0030g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+8764C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113364 | ||||||
| chr22:19113382
|
TA | T | 125 | a0001c0001t0001g0284a0001c0001t0010g0113a0001c0001t0010g0118others(122): Show | 131 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.79+8745delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113382 | ||||||
| chr22:19113382
|
TAA | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+8744_79+8745del others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113382 | ||||||
| chr22:19113388
|
A | T | 3 | a0001c0001t0001g0283a0001c0001t0005g0209a0001c0001t0005g0279 | 3 | HG03453.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.79+8740T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113388 | ||||||
| chr22:19113442
|
C | A | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+8686G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113442 | ||||||
| chr22:19113474
|
G | A | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+8654C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113474 | ||||||
| chr22:19113510
|
C | A | 11 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+8618G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113510 | ||||||
| chr22:19113620
|
A | C | 1 | a0002c0002t0009g0104 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79+8508T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113620 | ||||||
| chr22:19113626
|
G | A | 1 | a0001c0001t0005g0262 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.79+8502C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113626 | ||||||
| chr22:19113725
|
G | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.79+8403C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113725 | ||||||
| chr22:19113819
|
G | A | 1 | a0002c0002t0013g0004 | 2 | HG01496.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.79+8309C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113819 | ||||||
| chr22:19113960
|
G | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+8168C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113960 | ||||||
| chr22:19113962
|
G | T | 1 | a0002c0002t0003g0048 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.79+8166C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19113962 | ||||||
| chr22:19114038
|
A | G | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+8090T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114038 | ||||||
| chr22:19114062
|
G | GA | 13 | a0001c0001t0001g0206a0001c0001t0001g0263a0001c0001t0001g0311others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+8065dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114062 | ||||||
| chr22:19114062
|
GA | G | 10 | a0001c0001t0001g0208a0001c0001t0001g0272a0001c0001t0001g0274others(7): Show | 10 | HG02896.hp1 HG02897.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+8065delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114062 | ||||||
| chr22:19114062
|
GAAAA | G | 121 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(118): Show | 127 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.79+8062_79+8065del others(4): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114062 | ||||||
| chr22:19114063
|
A | G | 1 | a0001c0001t0016g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79+8065T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114063 | ||||||
| chr22:19114151
|
G | GA | 56 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(53): Show | 57 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.79+7976_79+7977ins others(1): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114151 | ||||||
| chr22:19114152
|
G | A | 154 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(151): Show | 160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.79+7976C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114152 | ||||||
| chr22:19114338
|
C | T | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+7790G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114338 | ||||||
| chr22:19114443
|
A | G | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+7685T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114443 | ||||||
| chr22:19114465
|
A | G | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+7663T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114465 | ||||||
| chr22:19114538
|
A | G | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+7590T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114538 | ||||||
| chr22:19114596
|
C | A | 1 | a0001c0001t0001g0321 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.79+7532G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114596 | ||||||
| chr22:19114604
|
C | G | 1 | a0002c0002t0002g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.79+7524G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114604 | ||||||
| chr22:19114750
|
C | T | 1 | a0001c0001t0010g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.79+7378G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114750 | ||||||
| chr22:19114772
|
T | G | 2 | a0002c0002t0002g0175a0002c0002t0002g0176 | 2 | HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.79+7356A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19114772 | ||||||
| chr22:19115069
|
G | C | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+7059C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115069 | ||||||
| chr22:19115186
|
G | A | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.79+6942C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115186 | ||||||
| chr22:19115264
|
C | T | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+6864G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115264 | ||||||
| chr22:19115309
|
C | G | 1 | a0001c0001t0005g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.79+6819G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115309 | ||||||
| chr22:19115507
|
C | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.79+6621G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115507 | ||||||
| chr22:19115574
|
T | G | 1 | a0001c0001t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.79+6554A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115574 | ||||||
| chr22:19115600
|
G | C | 1 | a0001c0001t0010g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79+6528C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115600 | ||||||
| chr22:19115746
|
G | T | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.79+6382C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115746 | ||||||
| chr22:19115757
|
G | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+6371C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115757 | ||||||
| chr22:19115785
|
T | G | 307 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0208others(304): Show | 316 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.79+6343A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115785 | ||||||
| chr22:19115834
|
T | C | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+6294A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115834 | ||||||
| chr22:19115956
|
C | A | 2 | a0002c0005t0043g0138a0002c0005t0044g0137 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.79+6172G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19115956 | ||||||
| chr22:19116050
|
T | C | 1 | a0002c0002t0033g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.79+6078A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116050 | ||||||
| chr22:19116085
|
C | G | 124 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(121): Show | 130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.79+6043G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116085 | ||||||
| chr22:19116352
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.79+5776C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116352 | ||||||
| chr22:19116464
|
T | C | 1 | a0002c0002t0002g0006 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.79+5664A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116464 | ||||||
| chr22:19116673
|
A | T | 154 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(151): Show | 160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.79+5455T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116673 | ||||||
| chr22:19116779
|
G | A | 2 | a0001c0004t0023g0127a0001c0004t0023g0132 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.79+5349C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116779 | ||||||
| chr22:19116811
|
C | T | 53 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(50): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.79+5317G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116811 | ||||||
| chr22:19116926
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+5202A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116926 | ||||||
| chr22:19116954
|
GATCACCT others(3): Show |
G | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.79+5164_79+5173del others(10): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19116954 | ||||||
| chr22:19117022
|
G | T | 61 | a0002c0002t0002g0006a0002c0002t0002g0133a0002c0002t0002g0134others(58): Show | 64 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+5106C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117022 | ||||||
| chr22:19117062
|
T | C | 1 | a0002c0002t0013g0081 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.79+5066A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117062 | ||||||
| chr22:19117116
|
T | C | 1 | a0002c0002t0011g0331 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79+5012A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117116 | ||||||
| chr22:19117161
|
C | T | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+4967G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117161 | ||||||
| chr22:19117274
|
G | A | 63 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(60): Show | 66 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.79+4854C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117274 | ||||||
| chr22:19117364
|
T | G | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+4764A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117364 | ||||||
| chr22:19117413
|
C | G | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+4715G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117413 | ||||||
| chr22:19117437
|
C | G | 23 | a0002c0002t0003g0002a0002c0002t0003g0045a0002c0002t0003g0046others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.79+4691G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117437 | ||||||
| chr22:19117491
|
G | A | 6 | a0003c0003t0007g0015a0003c0003t0012g0013a0003c0003t0012g0014others(3): Show | 6 | HG00642.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+4637C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117491 | ||||||
| chr22:19117535
|
A | G | 1 | a0001c0001t0010g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+4593T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117535 | ||||||
| chr22:19117638
|
G | A | 4 | a0002c0005t0020g0135a0002c0005t0020g0136a0002c0005t0020g0191others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+4490C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117638 | ||||||
| chr22:19117646
|
A | C | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.79+4482T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117646 | ||||||
| chr22:19117671
|
G | T | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+4457C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117671 | ||||||
| chr22:19117705
|
C | A | 1 | a0002c0002t0003g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.79+4423G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117705 | ||||||
| chr22:19117760
|
T | C | 34 | a0001c0001t0016g0114a0001c0001t0016g0115a0001c0001t0016g0117others(31): Show | 35 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+4368A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117760 | ||||||
| chr22:19117810
|
A | T | 3 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.79+4318T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117810 | ||||||
| chr22:19117816
|
G | A | 1 | a0002c0002t0038g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.79+4312C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117816 | ||||||
| chr22:19117905
|
C | G | 1 | a0002c0005t0020g0191 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+4223G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19117905 | ||||||
| chr22:19118245
|
G | A | 1 | a0003c0003t0012g0018 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.79+3883C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118245 | ||||||
| chr22:19118254
|
AAAGTTAC others(270): Show |
A | 1 | a0003c0003t0008g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.79+3597_79+3873del | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118254 | ||||||
| chr22:19118266
|
G | C | 61 | a0001c0001t0050g0334a0002c0002t0003g0003a0002c0002t0003g0068others(58): Show | 64 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+3862C>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118266 | ||||||
| chr22:19118374
|
C | CA | 32 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(29): Show | 33 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.79+3753dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118374 | ||||||
| chr22:19118374
|
CA | C | 50 | a0001c0001t0001g0192a0001c0001t0010g0123a0001c0001t0010g0124others(47): Show | 51 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.79+3753delT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118374 | ||||||
| chr22:19118374
|
CAA | C | 34 | a0001c0001t0010g0113a0001c0001t0010g0119a0001c0001t0010g0120others(31): Show | 34 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.79+3752_79+3753del others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118374 | ||||||
| chr22:19118374
|
CAAA | C | 7 | a0001c0001t0010g0118a0003c0003t0007g0015a0003c0003t0012g0013others(4): Show | 7 | HG00642.hp1 HG01952.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+3751_79+3753del others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118374 | ||||||
| chr22:19118395
|
A | C | 6 | a0002c0002t0009g0084a0002c0002t0009g0085a0002c0002t0009g0086others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+3733T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118395 | ||||||
| chr22:19118453
|
G | T | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.79+3675C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118453 | ||||||
| chr22:19118540
|
C | T | 1 | a0002c0002t0003g0045 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.79+3588G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118540 | ||||||
| chr22:19118607
|
A | C | 147 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(144): Show | 154 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.79+3521T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118607 | ||||||
| chr22:19118631
|
C | T | 12 | a0002c0002t0004g0075a0002c0002t0004g0076a0002c0002t0004g0078others(9): Show | 13 | HG00544.hp1 HG00673.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+3497G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118631 | ||||||
| chr22:19118710
|
C | T | 2 | a0001c0001t0024g0111a0001c0001t0024g0112 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.79+3418G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118710 | ||||||
| chr22:19118952
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.79+3176G>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19118952 | ||||||
| chr22:19119154
|
A | T | 1 | a0003c0003t0026g0009 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.79+2974T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119154 | ||||||
| chr22:19119156
|
G | A | 1 | a0003c0003t0026g0009 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.79+2972C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119156 | ||||||
| chr22:19119341
|
A | T | 1 | a0003c0003t0026g0009 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.79+2787T>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119341 | ||||||
| chr22:19119377
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.79+2751G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119377 | ||||||
| chr22:19119503
|
A | C | 29 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(26): Show | 29 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.79+2625T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119503 | ||||||
| chr22:19119735
|
C | CA | 113 | a0001c0001t0001g0008a0001c0001t0001g0272a0001c0001t0001g0273others(110): Show | 115 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.79+2392dupT | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119735 | ||||||
| chr22:19119735
|
C | CAA | 94 | a0001c0001t0021g0322a0001c0001t0050g0334a0001c0004t0015g0128others(91): Show | 99 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.79+2391_79+2392dup others(2): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119735 | ||||||
| chr22:19119735
|
C | CAAA | 6 | a0002c0002t0002g0183a0002c0002t0004g0108a0002c0002t0006g0181others(3): Show | 6 | HG02723.hp2 HG03130.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+2390_79+2392dup others(3): Show |
DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119735 | ||||||
| chr22:19119759
|
T | G | 1 | a0003c0003t0026g0009 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.79+2369A>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119759 | ||||||
| chr22:19119760
|
G | A | 1 | a0003c0003t0008g0038 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.79+2368C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119760 | ||||||
| chr22:19119924
|
A | G | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.79+2204T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119924 | ||||||
| chr22:19119958
|
CG | C | 29 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(26): Show | 29 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.79+2169delC | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19119958 | ||||||
| chr22:19120083
|
A | G | 199 | a0001c0001t0010g0113a0001c0001t0010g0118a0001c0001t0010g0119others(196): Show | 206 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.79+2045T>C | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120083 | ||||||
| chr22:19120084
|
C | T | 1 | a0002c0002t0002g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.79+2044G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120084 | ||||||
| chr22:19120116
|
C | A | 1 | a0002c0002t0004g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+2012G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120116 | ||||||
| chr22:19120195
|
G | A | 28 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(25): Show | 28 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.79+1933C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120195 | ||||||
| chr22:19120196
|
G | A | 1 | a0003c0003t0026g0009 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.79+1932C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120196 | ||||||
| chr22:19120253
|
C | A | 29 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(26): Show | 29 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.79+1875G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120253 | ||||||
| chr22:19120286
|
C | T | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+1842G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120286 | ||||||
| chr22:19120531
|
T | C | 7 | a0002c0002t0006g0001a0002c0002t0006g0184a0002c0002t0006g0185others(4): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+1597A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120531 | ||||||
| chr22:19120585
|
G | T | 86 | a0001c0001t0050g0334a0002c0002t0003g0002a0002c0002t0003g0003others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.79+1543C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120585 | ||||||
| chr22:19120853
|
T | C | 1 | a0001c0001t0001g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.79+1275A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120853 | ||||||
| chr22:19120971
|
G | A | 1 | a0002c0002t0002g0190 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.79+1157C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19120971 | ||||||
| chr22:19121035
|
T | C | 177 | a0001c0001t0050g0334a0002c0002t0002g0006a0002c0002t0002g0133others(174): Show | 184 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.79+1093A>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19121035 | ||||||
| chr22:19121475
|
G | A | 1 | a0002c0005t0020g0191 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+653C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19121475 | ||||||
| chr22:19121602
|
G | T | 1 | a0003c0003t0026g0009 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.79+526C>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19121602 | ||||||
| chr22:19121643
|
G | A | 1 | a0001c0001t0052g0335 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.79+485C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19121643 | ||||||
| chr22:19121776
|
G | A | 1 | a0002c0002t0039g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+352C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19121776 | ||||||
| chr22:19121813
|
C | T | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+315G>A | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19121813 | ||||||
| chr22:19122003
|
G | A | 7 | a0001c0004t0015g0128a0001c0004t0015g0129a0001c0004t0015g0130others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+125C>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19122003 | ||||||
| chr22:19122084
|
C | A | 30 | a0003c0003t0007g0012a0003c0003t0007g0015a0003c0003t0007g0020others(27): Show | 30 | HG00642.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.79+44G>T | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19122084 | ||||||
| chr22:19122096
|
A | C | 166 | a0001c0001t0016g0044a0002c0002t0002g0006a0002c0002t0002g0133others(163): Show | 173 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.79+32T>G | DGCR2 | ENSG00000070413.21 | transcript | ENST00000263196.12 | protein_coding | 1/9 | chr22 | 19122096 |