| geneid | 2078 |
|---|---|
| ensemblid | ENSG00000157554.20 |
| hgncid | 3446 |
| symbol | ERG |
| name | ETS transcription factor ERG |
| refseq_nuc | NM_182918.4 |
| refseq_prot | NP_891548.1 |
| ensembl_nuc | ENST00000288319.12 |
| ensembl_prot | ENSP00000288319.7 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 38380036 |
| end | 38498477 |
| strand | - |
| ver | v1.2 |
| region | chr21:38380036-38498477 |
| region5000 | chr21:38375036-38503477 |
| regionname0 | ERG_chr21_38380036_38498477 |
| regionname5000 | ERG_chr21_38375036_38503477 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 479 | 358 | 79 | 66 | 162 | 14 | 35 | 118 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0002 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0003 | 0/0 | 479 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1440 | 352 | 76 | 65 | 162 | 13 | 34 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| c0002 | 0/0 | 1440 | 3 | 2 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| c0003 | 0/0 | 1440 | 2 | 1 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| c0004 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| c0005 | 0/0 | 1440 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| c0006 | 0/0 | 1440 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3465 | 160 | 35 | 29 | 75 | 5 | 16 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0002 | 0/1 | 3460 | 64 | 25 | 9 | 27 | 0 | 2 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0003 | 0/0 | 3460 | 46 | 4 | 10 | 18 | 5 | 9 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0004 | 1/0 | 3465 | 29 | 1 | 6 | 16 | 3 | 2 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0005 | 0/0 | 3460 | 8 | 1 | 1 | 6 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0006 | 0/0 | 3460 | 7 | 1 | 1 | 3 | 0 | 2 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0007 | 0/0 | 3460 | 5 | 0 | 4 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0008 | 0/0 | 3464 | 5 | 0 | 1 | 4 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0009 | 0/0 | 3460 | 4 | 0 | 0 | 4 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0010 | 0/0 | 3465 | 4 | 0 | 1 | 0 | 1 | 2 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0011 | 0/0 | 3460 | 4 | 4 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0012 | 0/0 | 3461 | 3 | 2 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0013 | 0/0 | 3460 | 2 | 0 | 0 | 2 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0014 | 0/0 | 3460 | 2 | 0 | 1 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0015 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0016 | 0/0 | 3460 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0017 | 0/0 | 3460 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0018 | 0/0 | 3464 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0019 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0020 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0021 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0022 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0023 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0024 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0025 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0026 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0027 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0028 | 0/0 | 3460 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0029 | 0/0 | 3460 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0030 | 0/0 | 3460 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| t0031 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1440 | 352 | 76 | 65 | 162 | 13 | 34 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0002 | 0/0 | 1440 | 3 | 2 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0003 | 0/0 | 1440 | 2 | 1 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0006 | 0/0 | 1440 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0002c0004 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0003c0005 | 0/0 | 1440 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4904 | 157 | 34 | 29 | 75 | 5 | 14 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0002 | 0/1 | 4899 | 64 | 25 | 9 | 27 | 0 | 2 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0003 | 0/0 | 4899 | 45 | 3 | 10 | 18 | 5 | 9 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0004 | 1/0 | 4904 | 29 | 1 | 6 | 16 | 3 | 2 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0005 | 0/0 | 4899 | 8 | 1 | 1 | 6 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0006 | 0/0 | 4899 | 7 | 1 | 1 | 3 | 0 | 2 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0007 | 0/0 | 4899 | 5 | 0 | 4 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0008 | 0/0 | 4903 | 5 | 0 | 1 | 4 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0009 | 0/0 | 4899 | 4 | 0 | 0 | 4 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0010 | 0/0 | 4904 | 3 | 0 | 1 | 0 | 0 | 2 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0011 | 0/0 | 4899 | 4 | 4 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0013 | 0/0 | 4899 | 2 | 0 | 0 | 2 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0014 | 0/0 | 4899 | 2 | 0 | 1 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0015 | 0/0 | 4904 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0016 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0017 | 0/0 | 4899 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0018 | 0/0 | 4903 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0019 | 0/0 | 4904 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0020 | 0/0 | 4904 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0021 | 0/0 | 4904 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0022 | 0/0 | 4904 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0023 | 0/0 | 4904 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0024 | 0/0 | 4904 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0025 | 0/0 | 4904 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0026 | 0/0 | 4904 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0027 | 0/0 | 4904 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0028 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0029 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0030 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0001t0031 | 0/0 | 4904 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0002t0012 | 0/0 | 4900 | 3 | 2 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0003t0001 | 0/0 | 4904 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0003t0010 | 0/0 | 4904 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0001c0006t0001 | 0/0 | 4904 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0002c0004t0003 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| a0003c0005t0001 | 0/0 | 4904 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | copy fasta | chr21 | 38375036 | 38503477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0009g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0009g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0009g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0010g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0011g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0013g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0014g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0014g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0015g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0017g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0018g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0019g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0021g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0022g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0023g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0024g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0025g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0026g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0027g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0028g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0029g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0030g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0001t0031g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0002t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0002t0012g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0002t0012g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0003t0010g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0001c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0002c0004t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| a0003c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0266 | EUR | GBR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0040 | EUR | GBR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0230 | EUR | FIN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00323 | hp1 | a0001 | c0003 | t0010 | g0251 | EUR | FIN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0024 | EUR | FIN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00408 | hp1 | a0001 | c0001 | t0013 | g0093 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0038 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01106 | hp2 | a0001 | c0001 | t0026 | g0125 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0247 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0032 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01361 | hp1 | a0001 | c0001 | t0024 | g0092 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01361 | hp2 | a0001 | c0002 | t0012 | g0294 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | IBS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0270 | EUR | IBS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0031 | EUR | IBS | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01978 | hp1 | a0001 | c0001 | t0014 | g0075 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0011 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02027 | hp2 | a0001 | c0001 | t0008 | g0297 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02129 | hp2 | a0001 | c0001 | t0015 | g0037 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0022 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CDX | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | CDX | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0345 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02273 | hp2 | a0001 | c0001 | t0008 | g0071 | AMR | PEL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02280 | hp1 | a0002 | c0004 | t0003 | g0356 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0343 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0320 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0048 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0279 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0293 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0342 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0347 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0324 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03098 | hp2 | a0001 | c0001 | t0029 | g0233 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0355 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03195 | hp1 | a0001 | c0001 | t0028 | g0284 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03225 | hp2 | a0001 | c0001 | t0022 | g0157 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0228 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03491 | hp2 | a0003 | c0005 | t0001 | g0102 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0272 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0232 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03516 | hp2 | a0001 | c0001 | t0031 | g0358 | AFR | ESN | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03669 | hp1 | a0001 | c0001 | t0021 | g0068 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03669 | hp2 | a0001 | c0001 | t0010 | g0192 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03704 | hp2 | a0001 | c0001 | t0010 | g0084 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0161 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0035 | SAS | BEB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03831 | hp2 | a0001 | c0001 | t0023 | g0339 | SAS | BEB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | BEB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0325 | SAS | BEB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0257 | SAS | STU | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0052 | SAS | BEB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG04184 | hp2 | a0001 | c0001 | t0025 | g0063 | SAS | BEB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0046 | SAS | STU | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | STU | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG04228 | hp1 | a0001 | c0006 | t0001 | g0177 | SAS | STU | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | STU | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | YRI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | YRI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | CHB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | CHB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0352 | AFR | YRI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | YRI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0171 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18948 | hp1 | a0001 | c0001 | t0009 | g0144 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18950 | hp1 | a0001 | c0001 | t0017 | g0034 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18954 | hp1 | a0001 | c0001 | t0009 | g0315 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18971 | hp1 | a0001 | c0001 | t0020 | g0042 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18989 | hp2 | a0001 | c0001 | t0009 | g0288 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18991 | hp2 | a0001 | c0001 | t0019 | g0047 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18993 | hp1 | a0001 | c0001 | t0013 | g0331 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0154 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | LWK | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19030 | hp2 | a0001 | c0001 | t0030 | g0256 | AFR | LWK | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0205 | AFR | LWK | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19054 | hp1 | a0001 | c0001 | t0008 | g0094 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19082 | hp1 | a0001 | c0001 | t0014 | g0083 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19090 | hp2 | a0001 | c0001 | t0018 | g0030 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | YRI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA19240 | hp2 | a0001 | c0002 | t0012 | g0181 | AFR | YRI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | ASW | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0069 | EUR | TSI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0201 | EUR | TSI | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | MSL | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | USA | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | USA | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA18955 | hp2 | a0001 | c0001 | t0008 | g0214 | EAS | JPT | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | USA | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | USA | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA21309 | hp1 | a0001 | c0001 | t0027 | g0346 | AFR | LWK | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0087 | REF | REF | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0014 | REF | REF | ERG_chr21_38375036_38503477 | ERG | chr21 | 38375036 | 38503477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:38391707
|
G | A | 1 | a0003 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.823C>T | p.Pro275Ser | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 8/10 | 920/4904 | 823/1440 | 275/479 | chr21 | 38391707 | ||
| chr21:38402573
|
C | T | 1 | a0002 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.657G>A | p.Met219Ile | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/10 | 754/4904 | 657/1440 | 219/479 | chr21 | 38402573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:38383685
|
G | A | 1 | a0001c0002 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.1158C>T | p.Tyr386Tyr | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1255/4904 | 1158/1440 | 386/479 | chr21 | 38383685 | ||
| chr21:38403546
|
G | A | 1 | a0001c0006 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.552C>T | p.Asn184Asn | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/10 | 649/4904 | 552/1440 | 184/479 | chr21 | 38403546 | ||
| chr21:38403636
|
G | A | 1 | a0001c0003 | 2 | HG00323.hp1 HG02896.hp2 |
synonymous_variant | LOW | c.462C>T | p.Asp154Asp | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/10 | 559/4904 | 462/1440 | 154/479 | chr21 | 38403636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:38380457
|
C | T | 1 | a0001c0001t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2946G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2946 | chr21 | 38380457 | |||||
| chr21:38380521
|
A | C | 1 | a0001c0001t0028 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2882T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2882 | chr21 | 38380521 | |||||
| chr21:38380559
|
G | A | 2 | a0001c0001t0011a0001c0001t0016 | 5 | HG02572.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2844C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2844 | chr21 | 38380559 | |||||
| chr21:38380564
|
A | G | 1 | a0001c0001t0029 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2839T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2839 | chr21 | 38380564 | |||||
| chr21:38380634
|
A | G | 2 | a0001c0001t0010a0001c0003t0010 | 4 | HG00323.hp1 HG01109.hp1 HG03669.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2769T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2769 | chr21 | 38380634 | |||||
| chr21:38380751
|
C | T | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(13): Show | 150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2652G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2652 | chr21 | 38380751 | |||||
| chr21:38380799
|
GAATAT | G | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(13): Show | 150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2599_*2603delATAT others(1): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2599 | chr21 | 38380799 | |||||
| chr21:38381095
|
C | T | 1 | a0001c0001t0024 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2308G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2308 | chr21 | 38381095 | |||||
| chr21:38381132
|
CT | C | 2 | a0001c0001t0008a0001c0001t0018 | 6 | HG02027.hp2 HG02273.hp2 NA18942.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2270delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2270 | chr21 | 38381132 | |||||
| chr21:38381207
|
A | T | 1 | a0001c0001t0023 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2196T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2196 | chr21 | 38381207 | |||||
| chr21:38381208
|
C | T | 2 | a0001c0001t0007a0001c0001t0014 | 7 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2195G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2195 | chr21 | 38381208 | |||||
| chr21:38381243
|
G | C | 1 | a0001c0001t0026 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2160C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2160 | chr21 | 38381243 | |||||
| chr21:38381260
|
T | C | 3 | a0001c0001t0011a0001c0001t0016a0001c0001t0029 | 6 | HG02572.hp1 HG02622.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2143A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2143 | chr21 | 38381260 | |||||
| chr21:38381285
|
C | T | 1 | a0001c0001t0013 | 2 | HG00408.hp1 NA18993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2118G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2118 | chr21 | 38381285 | |||||
| chr21:38381291
|
C | T | 1 | a0001c0001t0028 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2112G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2112 | chr21 | 38381291 | |||||
| chr21:38381360
|
T | C | 1 | a0001c0001t0030 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2043A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 2043 | chr21 | 38381360 | |||||
| chr21:38381424
|
A | C | 5 | a0001c0001t0003a0001c0001t0006a0001c0001t0013others(2): Show | 56 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1979T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1979 | chr21 | 38381424 | |||||
| chr21:38381450
|
T | C | 1 | a0001c0001t0027 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1953A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1953 | chr21 | 38381450 | |||||
| chr21:38381453
|
T | C | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(15): Show | 152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1950A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1950 | chr21 | 38381453 | |||||
| chr21:38381554
|
C | T | 1 | a0001c0001t0022 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1849G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1849 | chr21 | 38381554 | |||||
| chr21:38381934
|
T | TA | 1 | a0001c0002t0012 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1468dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1468 | chr21 | 38381934 | |||||
| chr21:38381957
|
A | G | 1 | a0001c0002t0012 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1446T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1446 | chr21 | 38381957 | |||||
| chr21:38382163
|
C | T | 2 | a0001c0001t0009a0001c0001t0017 | 5 | NA18948.hp1 NA18950.hp1 NA18954.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1240G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1240 | chr21 | 38382163 | |||||
| chr21:38382394
|
C | T | 1 | a0001c0001t0016 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1009G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 1009 | chr21 | 38382394 | |||||
| chr21:38382467
|
C | G | 1 | a0001c0001t0021 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 936 | chr21 | 38382467 | |||||
| chr21:38382873
|
A | C | 1 | a0001c0002t0012 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*530T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 530 | chr21 | 38382873 | |||||
| chr21:38383272
|
C | T | 1 | a0001c0001t0015 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*131G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 10/10 | 131 | chr21 | 38383272 | |||||
| chr21:38498386
|
G | A | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | 305 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(302): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/10 | chr21 | 38498386 | ||||||
| chr21:38498456
|
G | A | 1 | a0001c0001t0031 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/10 | 76 | chr21 | 38498456 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:38383988
|
T | C | 1 | a0001c0001t0004g0040 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.920-65A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38383988 | ||||||
| chr21:38384054
|
T | A | 51 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0062others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.920-131A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384054 | ||||||
| chr21:38384136
|
G | A | 1 | a0001c0001t0001g0329 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.920-213C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384136 | ||||||
| chr21:38384174
|
G | A | 1 | a0003c0005t0001g0102 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.920-251C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384174 | ||||||
| chr21:38384573
|
AT | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0127a0001c0001t0001g0143others(5): Show | 8 | HG01069.hp2 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-651delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384573 | ||||||
| chr21:38384575
|
T | A | 6 | a0001c0001t0011g0205a0001c0001t0011g0232a0001c0001t0011g0279others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-652A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384575 | ||||||
| chr21:38384676
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.920-753T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384676 | ||||||
| chr21:38384834
|
G | GA | 13 | a0001c0001t0001g0237a0001c0001t0002g0295a0001c0001t0002g0322others(10): Show | 13 | HG01515.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.920-912dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384834 | ||||||
| chr21:38384834
|
G | GAA | 16 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(13): Show | 16 | HG00735.hp1 HG01243.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.920-913_920-912dup others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384834 | ||||||
| chr21:38384969
|
G | A | 1 | a0001c0001t0007g0011 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.920-1046C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38384969 | ||||||
| chr21:38385045
|
A | G | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920-1122T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385045 | ||||||
| chr21:38385134
|
T | A | 4 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-1211A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385134 | ||||||
| chr21:38385340
|
A | G | 5 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0002t0012g0181others(2): Show | 5 | HG00735.hp1 HG01361.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-1417T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385340 | ||||||
| chr21:38385378
|
G | A | 21 | a0001c0001t0003g0062a0001c0001t0003g0088a0001c0001t0003g0100others(18): Show | 21 | HG00408.hp1 HG00558.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.920-1455C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385378 | ||||||
| chr21:38385454
|
G | A | 1 | a0001c0001t0003g0321 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.920-1531C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385454 | ||||||
| chr21:38385572
|
A | T | 1 | a0001c0001t0008g0297 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.920-1649T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385572 | ||||||
| chr21:38385730
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.920-1807A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385730 | ||||||
| chr21:38385787
|
A | C | 1 | a0001c0001t0001g0330 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.920-1864T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385787 | ||||||
| chr21:38385951
|
C | T | 1 | a0001c0001t0015g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.920-2028G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385951 | ||||||
| chr21:38385987
|
C | T | 5 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0002t0012g0181others(2): Show | 5 | HG00735.hp1 HG01361.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-2064G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38385987 | ||||||
| chr21:38386001
|
G | A | 1 | a0001c0001t0011g0279 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.920-2078C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386001 | ||||||
| chr21:38386185
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.920-2262T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386185 | ||||||
| chr21:38386226
|
T | C | 5 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0002t0012g0181others(2): Show | 5 | HG00735.hp1 HG01361.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-2303A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386226 | ||||||
| chr21:38386510
|
A | T | 4 | a0001c0001t0002g0164a0001c0001t0002g0170a0001c0001t0002g0204others(1): Show | 4 | NA18962.hp1 NA18967.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-2587T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386510 | ||||||
| chr21:38386679
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.920-2756C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386679 | ||||||
| chr21:38386789
|
A | AT | 36 | a0001c0001t0002g0078a0001c0001t0002g0081a0001c0001t0002g0111others(33): Show | 37 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-2867dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386789 | ||||||
| chr21:38386789
|
AT | A | 59 | a0001c0001t0001g0064a0001c0001t0002g0002a0001c0001t0002g0085others(56): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.920-2867delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386789 | ||||||
| chr21:38386789
|
ATT | A | 23 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0160others(20): Show | 23 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.920-2868_920-2867d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386789 | ||||||
| chr21:38386791
|
T | G | 5 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0002t0012g0181others(2): Show | 5 | HG00735.hp1 HG01361.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-2868A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386791 | ||||||
| chr21:38386938
|
G | A | 37 | a0001c0001t0002g0078a0001c0001t0002g0081a0001c0001t0002g0111others(34): Show | 38 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.920-3015C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38386938 | ||||||
| chr21:38387076
|
GA | G | 15 | a0001c0001t0002g0002a0001c0001t0002g0085a0001c0001t0002g0087others(12): Show | 16 | HG00639.hp1 HG00642.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.920-3154delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387076 | ||||||
| chr21:38387185
|
G | A | 1 | a0001c0001t0003g0325 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.920-3262C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387185 | ||||||
| chr21:38387393
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.920-3470T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387393 | ||||||
| chr21:38387404
|
G | A | 4 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-3481C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387404 | ||||||
| chr21:38387491
|
G | A | 7 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(4): Show | 7 | HG01074.hp2 HG01081.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+3504C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387491 | ||||||
| chr21:38387546
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0354 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.919+3449C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387546 | ||||||
| chr21:38387559
|
T | A | 8 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0179others(5): Show | 8 | HG01361.hp2 HG02622.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+3436A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387559 | ||||||
| chr21:38387652
|
T | C | 6 | a0001c0001t0002g0002a0001c0001t0002g0085a0001c0001t0002g0087others(3): Show | 7 | HG00639.hp1 HG00642.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+3343A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387652 | ||||||
| chr21:38387707
|
T | C | 1 | a0001c0001t0002g0301 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.919+3288A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387707 | ||||||
| chr21:38387783
|
G | A | 6 | a0001c0001t0002g0002a0001c0001t0002g0085a0001c0001t0002g0087others(3): Show | 7 | HG00639.hp1 HG00642.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+3212C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387783 | ||||||
| chr21:38387865
|
G | A | 1 | a0001c0001t0003g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.919+3130C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38387865 | ||||||
| chr21:38388156
|
T | C | 1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.919+2839A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38388156 | ||||||
| chr21:38388223
|
T | C | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.919+2772A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38388223 | ||||||
| chr21:38388789
|
C | T | 187 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(184): Show | 189 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.919+2206G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38388789 | ||||||
| chr21:38388839
|
G | T | 17 | a0001c0001t0002g0109a0001c0001t0002g0139a0001c0001t0002g0146others(14): Show | 17 | HG00323.hp1 HG00609.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+2156C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38388839 | ||||||
| chr21:38388863
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0319 | 2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.919+2132G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38388863 | ||||||
| chr21:38388866
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.919+2129A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38388866 | ||||||
| chr21:38388896
|
A | G | 5 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0001g0253others(2): Show | 5 | HG02486.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+2099T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38388896 | ||||||
| chr21:38389154
|
C | G | 4 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+1841G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38389154 | ||||||
| chr21:38389229
|
T | A | 283 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.919+1766A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38389229 | ||||||
| chr21:38389265
|
G | C | 1 | a0001c0001t0003g0118 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.919+1730C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38389265 | ||||||
| chr21:38389399
|
T | A | 9 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+1596A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38389399 | ||||||
| chr21:38389501
|
C | T | 1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.919+1494G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38389501 | ||||||
| chr21:38389615
|
A | G | 5 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0257others(2): Show | 5 | HG00280.hp2 HG01256.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+1380T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38389615 | ||||||
| chr21:38389657
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.919+1338C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38389657 | ||||||
| chr21:38389952
|
T | C | 3 | a0001c0002t0012g0181a0001c0002t0012g0228a0001c0002t0012g0294 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.919+1043A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38389952 | ||||||
| chr21:38390119
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0295 | 2 | HG00735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.919+876C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38390119 | ||||||
| chr21:38390461
|
G | T | 1 | a0001c0001t0001g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.919+534C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38390461 | ||||||
| chr21:38390522
|
G | A | 1 | a0001c0001t0001g0334 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.919+473C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38390522 | ||||||
| chr21:38390613
|
G | C | 2 | a0001c0001t0010g0192a0001c0001t0010g0247 | 2 | HG01109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.919+382C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38390613 | ||||||
| chr21:38390659
|
C | T | 1 | a0001c0001t0014g0075 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.919+336G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38390659 | ||||||
| chr21:38390844
|
C | A | 1 | a0001c0001t0001g0311 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.919+151G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38390844 | ||||||
| chr21:38390961
|
T | C | 36 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(33): Show | 36 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.919+34A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 9/9 | chr21 | 38390961 | ||||||
| chr21:38391088
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.872-46T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 8/9 | chr21 | 38391088 | ||||||
| chr21:38391211
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0278 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.872-169C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 8/9 | chr21 | 38391211 | ||||||
| chr21:38391432
|
C | A | 92 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.871+227G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 8/9 | chr21 | 38391432 | ||||||
| chr21:38391576
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.871+83G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 8/9 | chr21 | 38391576 | ||||||
| chr21:38391614
|
C | G | 4 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+45G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 8/9 | chr21 | 38391614 | ||||||
| chr21:38391760
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.815-45C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 7/9 | chr21 | 38391760 | ||||||
| chr21:38391822
|
T | G | 1 | a0001c0001t0001g0329 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.815-107A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 7/9 | chr21 | 38391822 | ||||||
| chr21:38391955
|
T | TA | 68 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(65): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.815-241dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 7/9 | chr21 | 38391955 | ||||||
| chr21:38391955
|
T | TAA | 16 | a0001c0001t0002g0109a0001c0001t0002g0139a0001c0001t0002g0146others(13): Show | 16 | HG00323.hp1 HG00609.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.815-242_815-241dup others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 7/9 | chr21 | 38391955 | ||||||
| chr21:38392094
|
A | T | 175 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(172): Show | 177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.814+282T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 7/9 | chr21 | 38392094 | ||||||
| chr21:38392266
|
A | G | 3 | a0001c0002t0012g0181a0001c0002t0012g0228a0001c0002t0012g0294 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.814+110T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 7/9 | chr21 | 38392266 | ||||||
| chr21:38392289
|
T | A | 83 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.814+87A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 7/9 | chr21 | 38392289 | ||||||
| chr21:38392339
|
G | C | 3 | a0001c0002t0012g0181a0001c0002t0012g0228a0001c0002t0012g0294 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.814+37C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 7/9 | chr21 | 38392339 | ||||||
| chr21:38392479
|
C | G | 1 | a0001c0001t0010g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.746-35G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392479 | ||||||
| chr21:38392493
|
A | G | 1 | a0001c0001t0003g0310 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.746-49T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392493 | ||||||
| chr21:38392501
|
C | T | 9 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-57G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392501 | ||||||
| chr21:38392515
|
T | C | 83 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.746-71A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392515 | ||||||
| chr21:38392594
|
T | C | 11 | a0001c0001t0003g0160a0001c0001t0003g0188a0001c0001t0003g0198others(8): Show | 11 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.746-150A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392594 | ||||||
| chr21:38392643
|
C | T | 17 | a0001c0001t0002g0109a0001c0001t0002g0139a0001c0001t0002g0146others(14): Show | 17 | HG00323.hp1 HG00609.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.746-199G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392643 | ||||||
| chr21:38392666
|
G | A | 92 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.746-222C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392666 | ||||||
| chr21:38392765
|
T | A | 9 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-321A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392765 | ||||||
| chr21:38392862
|
T | C | 92 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.746-418A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392862 | ||||||
| chr21:38392964
|
A | G | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.746-520T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38392964 | ||||||
| chr21:38393045
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.746-601G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38393045 | ||||||
| chr21:38393283
|
A | G | 1 | a0001c0001t0002g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.746-839T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38393283 | ||||||
| chr21:38393588
|
C | T | 66 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.746-1144G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38393588 | ||||||
| chr21:38393781
|
C | T | 2 | a0001c0001t0010g0192a0001c0001t0010g0247 | 2 | HG01109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.746-1337G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38393781 | ||||||
| chr21:38393920
|
C | T | 4 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-1476G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38393920 | ||||||
| chr21:38394109
|
C | T | 91 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.746-1665G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394109 | ||||||
| chr21:38394220
|
C | T | 9 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-1776G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394220 | ||||||
| chr21:38394289
|
T | G | 9 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-1845A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394289 | ||||||
| chr21:38394354
|
ATC | A | 9 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-1912_746-1911d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394354 | ||||||
| chr21:38394369
|
T | G | 9 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-1925A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394369 | ||||||
| chr21:38394431
|
C | A | 9 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(6): Show | 9 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-1987G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394431 | ||||||
| chr21:38394499
|
C | T | 83 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.746-2055G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394499 | ||||||
| chr21:38394504
|
C | T | 11 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(8): Show | 11 | HG00323.hp2 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.746-2060G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394504 | ||||||
| chr21:38394526
|
G | A | 11 | a0001c0001t0001g0058a0001c0001t0002g0002a0001c0001t0002g0085others(8): Show | 12 | HG00639.hp1 HG00642.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.746-2082C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394526 | ||||||
| chr21:38394575
|
C | A | 92 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.746-2131G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394575 | ||||||
| chr21:38394647
|
T | C | 92 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.746-2203A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394647 | ||||||
| chr21:38394747
|
G | T | 1 | a0001c0001t0003g0118 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.746-2303C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394747 | ||||||
| chr21:38394944
|
T | A | 1 | a0001c0001t0009g0144 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.746-2500A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394944 | ||||||
| chr21:38394945
|
A | T | 1 | a0001c0001t0009g0144 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.746-2501T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394945 | ||||||
| chr21:38394997
|
C | G | 1 | a0001c0001t0016g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.746-2553G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38394997 | ||||||
| chr21:38395133
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.746-2689C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395133 | ||||||
| chr21:38395134
|
C | T | 1 | a0001c0002t0012g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.746-2690G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395134 | ||||||
| chr21:38395266
|
C | G | 1 | a0001c0001t0002g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.746-2822G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395266 | ||||||
| chr21:38395328
|
C | T | 46 | a0001c0001t0001g0130a0001c0001t0001g0153a0001c0001t0001g0313others(43): Show | 47 | HG00438.hp2 HG00544.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.746-2884G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395328 | ||||||
| chr21:38395446
|
C | T | 3 | a0001c0002t0012g0181a0001c0002t0012g0228a0001c0002t0012g0294 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.746-3002G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395446 | ||||||
| chr21:38395459
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.746-3015G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395459 | ||||||
| chr21:38395559
|
C | A | 2 | a0001c0001t0001g0211a0001c0001t0004g0051 | 2 | HG01975.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.746-3115G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395559 | ||||||
| chr21:38395641
|
T | C | 6 | a0001c0001t0003g0069a0001c0001t0003g0229a0001c0001t0003g0230others(3): Show | 6 | HG00280.hp2 HG01256.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.746-3197A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395641 | ||||||
| chr21:38395701
|
G | A | 1 | a0001c0001t0028g0284 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.746-3257C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395701 | ||||||
| chr21:38395732
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.746-3288C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395732 | ||||||
| chr21:38395935
|
A | AC | 4 | a0001c0001t0001g0060a0001c0001t0002g0204a0001c0001t0003g0310others(1): Show | 4 | HG02148.hp1 NA19078.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.746-3492dupG | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395935 | ||||||
| chr21:38395951
|
G | A | 1 | a0001c0001t0006g0006 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.746-3507C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395951 | ||||||
| chr21:38395952
|
C | T | 66 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.746-3508G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38395952 | ||||||
| chr21:38396012
|
T | G | 3 | a0001c0002t0012g0181a0001c0002t0012g0228a0001c0002t0012g0294 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.746-3568A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396012 | ||||||
| chr21:38396069
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.746-3625T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396069 | ||||||
| chr21:38396171
|
G | GA | 26 | a0001c0001t0002g0109a0001c0001t0002g0134a0001c0001t0002g0139others(23): Show | 26 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.746-3728dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396171 | ||||||
| chr21:38396183
|
T | G | 1 | a0001c0001t0003g0162 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.746-3739A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396183 | ||||||
| chr21:38396192
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.746-3748G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396192 | ||||||
| chr21:38396262
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.746-3818A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396262 | ||||||
| chr21:38396352
|
A | G | 93 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(90): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.746-3908T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396352 | ||||||
| chr21:38396399
|
G | A | 1 | a0001c0001t0006g0035 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.746-3955C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396399 | ||||||
| chr21:38396407
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.746-3963T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396407 | ||||||
| chr21:38396525
|
T | C | 1 | a0001c0001t0002g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.745+4049A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396525 | ||||||
| chr21:38396729
|
G | C | 1 | a0001c0001t0003g0337 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.745+3845C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396729 | ||||||
| chr21:38396828
|
T | C | 83 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.745+3746A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396828 | ||||||
| chr21:38396839
|
G | C | 6 | a0001c0001t0002g0002a0001c0001t0002g0085a0001c0001t0002g0087others(3): Show | 7 | HG00639.hp1 HG00642.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.745+3735C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396839 | ||||||
| chr21:38396865
|
T | G | 1 | a0001c0001t0002g0249 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.745+3709A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396865 | ||||||
| chr21:38396915
|
TAA | T | 12 | a0001c0001t0001g0259a0001c0001t0002g0134a0001c0001t0002g0295others(9): Show | 12 | HG00735.hp1 HG01361.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.745+3657_745+3658d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396915 | ||||||
| chr21:38396918
|
A | T | 4 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.745+3656T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396918 | ||||||
| chr21:38396963
|
G | C | 10 | a0001c0001t0001g0095a0001c0001t0001g0150a0001c0001t0001g0155others(7): Show | 10 | NA18939.hp1 NA18951.hp2 NA18970.hp2 others(7): Show |
intron_variant | MODIFIER | c.745+3611C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38396963 | ||||||
| chr21:38397101
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.745+3473C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397101 | ||||||
| chr21:38397110
|
T | C | 83 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.745+3464A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397110 | ||||||
| chr21:38397131
|
G | A | 8 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0082others(5): Show | 8 | HG02129.hp1 HG02132.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.745+3443C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397131 | ||||||
| chr21:38397191
|
T | C | 83 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.745+3383A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397191 | ||||||
| chr21:38397224
|
C | T | 16 | a0001c0001t0001g0259a0001c0001t0002g0134a0001c0001t0002g0295others(13): Show | 16 | HG00735.hp1 HG01167.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.745+3350G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397224 | ||||||
| chr21:38397268
|
A | G | 3 | a0001c0002t0012g0181a0001c0002t0012g0228a0001c0002t0012g0294 | 3 | HG01361.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.745+3306T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397268 | ||||||
| chr21:38397327
|
T | C | 83 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.745+3247A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397327 | ||||||
| chr21:38397470
|
C | A | 4 | a0001c0001t0001g0114a0001c0001t0001g0231a0001c0001t0001g0236others(1): Show | 4 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.745+3104G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397470 | ||||||
| chr21:38397472
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.745+3102G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397472 | ||||||
| chr21:38397490
|
C | A | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.745+3084G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397490 | ||||||
| chr21:38397490
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.745+3084G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397490 | ||||||
| chr21:38397596
|
C | CA | 65 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.745+2977dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397596 | ||||||
| chr21:38397596
|
C | CAA | 22 | a0001c0001t0002g0109a0001c0001t0002g0139a0001c0001t0002g0146others(19): Show | 22 | HG00323.hp1 HG00609.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+2976_745+2977d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397596 | ||||||
| chr21:38397596
|
CA | C | 158 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(155): Show | 160 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.745+2977delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397596 | ||||||
| chr21:38397596
|
CAA | C | 8 | a0001c0001t0001g0172a0001c0001t0001g0193a0001c0001t0001g0213others(5): Show | 8 | HG01257.hp2 HG01361.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.745+2976_745+2977d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397596 | ||||||
| chr21:38397756
|
T | C | 13 | a0001c0001t0001g0259a0001c0001t0002g0134a0001c0001t0002g0295others(10): Show | 13 | HG00735.hp1 HG01167.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.745+2818A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397756 | ||||||
| chr21:38397783
|
C | A | 1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.745+2791G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397783 | ||||||
| chr21:38397783
|
C | G | 1 | a0001c0001t0002g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.745+2791G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397783 | ||||||
| chr21:38397895
|
G | C | 65 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.745+2679C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38397895 | ||||||
| chr21:38398047
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0295 | 2 | HG00735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.745+2527C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398047 | ||||||
| chr21:38398064
|
C | T | 8 | a0001c0001t0001g0150a0001c0001t0001g0155a0001c0001t0001g0212others(5): Show | 8 | NA18939.hp1 NA18970.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.745+2510G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398064 | ||||||
| chr21:38398214
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0295 | 2 | HG00735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.745+2360C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398214 | ||||||
| chr21:38398241
|
CT | C | 6 | a0001c0001t0002g0134a0001c0001t0002g0295a0001c0001t0003g0241others(3): Show | 6 | HG00735.hp1 HG01167.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.745+2332delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398241 | ||||||
| chr21:38398304
|
A | ATAAC | 13 | a0001c0001t0001g0072a0001c0001t0001g0091a0001c0001t0001g0097others(10): Show | 13 | HG01243.hp1 HG02027.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.745+2266_745+2269d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398304 | ||||||
| chr21:38398337
|
G | C | 1 | a0001c0001t0003g0321 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.745+2237C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398337 | ||||||
| chr21:38398360
|
C | G | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.745+2214G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398360 | ||||||
| chr21:38398364
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745+2210A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398364 | ||||||
| chr21:38398442
|
T | C | 113 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(110): Show | 114 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.745+2132A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398442 | ||||||
| chr21:38398552
|
A | G | 1 | a0001c0001t0002g0260 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.745+2022T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398552 | ||||||
| chr21:38398934
|
A | T | 96 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.745+1640T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398934 | ||||||
| chr21:38398937
|
T | C | 1 | a0001c0006t0001g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.745+1637A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38398937 | ||||||
| chr21:38399021
|
C | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0295 | 2 | HG00735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.745+1553G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38399021 | ||||||
| chr21:38399233
|
G | A | 4 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.745+1341C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38399233 | ||||||
| chr21:38399452
|
T | G | 16 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.745+1122A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38399452 | ||||||
| chr21:38399554
|
T | C | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.745+1020A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38399554 | ||||||
| chr21:38399581
|
C | A | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.745+993G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38399581 | ||||||
| chr21:38399654
|
G | A | 1 | a0001c0001t0002g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.745+920C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38399654 | ||||||
| chr21:38399707
|
T | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0097a0001c0001t0001g0138others(2): Show | 5 | HG01243.hp1 HG02683.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+867A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38399707 | ||||||
| chr21:38399801
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.745+773G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38399801 | ||||||
| chr21:38400141
|
A | G | 3 | a0001c0001t0001g0309a0001c0001t0008g0094a0001c0001t0008g0214 | 3 | NA18955.hp2 NA18972.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.745+433T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38400141 | ||||||
| chr21:38400473
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.745+101G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38400473 | ||||||
| chr21:38400511
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.745+63C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 6/9 | chr21 | 38400511 | ||||||
| chr21:38400696
|
C | T | 3 | a0001c0001t0003g0221a0001c0001t0003g0298a0001c0001t0011g0320 | 3 | HG02572.hp1 NA18939.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.674-51G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38400696 | ||||||
| chr21:38400733
|
G | A | 1 | a0001c0001t0006g0006 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.674-88C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38400733 | ||||||
| chr21:38400757
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.674-112G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38400757 | ||||||
| chr21:38400835
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.674-190G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38400835 | ||||||
| chr21:38400878
|
GT | G | 4 | a0001c0001t0002g0254a0001c0001t0002g0265a0001c0001t0002g0349others(1): Show | 4 | HG02559.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-234delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38400878 | ||||||
| chr21:38400908
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0152 | 3 | NA18963.hp2 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.674-263G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38400908 | ||||||
| chr21:38400919
|
C | T | 17 | a0001c0001t0002g0109a0001c0001t0002g0139a0001c0001t0002g0146others(14): Show | 17 | HG00323.hp1 HG00609.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-274G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38400919 | ||||||
| chr21:38400930
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.674-285G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38400930 | ||||||
| chr21:38401235
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0135a0001c0001t0004g0039 | 3 | NA18964.hp2 NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.674-590A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38401235 | ||||||
| chr21:38401585
|
A | T | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.674-940T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38401585 | ||||||
| chr21:38401606
|
T | C | 83 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.673+951A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38401606 | ||||||
| chr21:38401668
|
G | A | 2 | a0001c0001t0011g0205a0001c0001t0011g0320 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.673+889C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38401668 | ||||||
| chr21:38401838
|
G | A | 1 | a0001c0001t0003g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.673+719C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38401838 | ||||||
| chr21:38401931
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0225 | 2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.673+626G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38401931 | ||||||
| chr21:38402190
|
C | A | 1 | a0001c0001t0028g0284 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.673+367G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38402190 | ||||||
| chr21:38402314
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.673+243G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38402314 | ||||||
| chr21:38402426
|
C | G | 101 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0067others(98): Show | 102 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.673+131G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38402426 | ||||||
| chr21:38402508
|
C | T | 1 | a0002c0004t0003g0356 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.673+49G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 5/9 | chr21 | 38402508 | ||||||
| chr21:38402670
|
G | GA | 19 | a0001c0001t0001g0120a0001c0001t0002g0109a0001c0001t0002g0139others(16): Show | 19 | HG00323.hp1 HG00609.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.593-34dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38402670 | ||||||
| chr21:38402712
|
C | CA | 47 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0076others(44): Show | 48 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.593-76dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38402712 | ||||||
| chr21:38402712
|
C | CAA | 16 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0119others(13): Show | 17 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.593-77_593-76dupTT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38402712 | ||||||
| chr21:38402712
|
CA | C | 78 | a0001c0001t0001g0090a0001c0001t0001g0120a0001c0001t0001g0211others(75): Show | 78 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.593-76delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38402712 | ||||||
| chr21:38402712
|
CAA | C | 10 | a0001c0001t0001g0258a0001c0001t0002g0126a0001c0001t0002g0134others(7): Show | 10 | HG00735.hp1 HG01361.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.593-77_593-76delTT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38402712 | ||||||
| chr21:38402728
|
A | G | 1 | a0001c0001t0025g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.593-91T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38402728 | ||||||
| chr21:38402757
|
G | A | 32 | a0001c0001t0001g0313a0001c0001t0001g0334a0001c0001t0002g0078others(29): Show | 33 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.593-120C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38402757 | ||||||
| chr21:38403121
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0351 | 2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.592+385G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38403121 | ||||||
| chr21:38403134
|
C | T | 2 | a0001c0001t0002g0134a0001c0001t0002g0295 | 2 | HG00735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.592+372G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38403134 | ||||||
| chr21:38403162
|
C | T | 167 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(164): Show | 168 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.592+344G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38403162 | ||||||
| chr21:38403352
|
C | T | 36 | a0001c0001t0001g0313a0001c0001t0001g0334a0001c0001t0002g0078others(33): Show | 37 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.592+154G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38403352 | ||||||
| chr21:38403450
|
C | T | 1 | a0001c0001t0002g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.592+56G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38403450 | ||||||
| chr21:38403451
|
A | G | 269 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.592+55T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 4/9 | chr21 | 38403451 | ||||||
| chr21:38403897
|
T | A | 1 | a0001c0001t0010g0192 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.389-188A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38403897 | ||||||
| chr21:38404000
|
C | A | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.389-291G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404000 | ||||||
| chr21:38404006
|
T | C | 11 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0140others(8): Show | 11 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.389-297A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404006 | ||||||
| chr21:38404042
|
A | G | 268 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.389-333T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404042 | ||||||
| chr21:38404535
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.389-826G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404535 | ||||||
| chr21:38404563
|
A | T | 73 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(70): Show | 73 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.389-854T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404563 | ||||||
| chr21:38404590
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0268 | 2 | HG00738.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.389-881G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404590 | ||||||
| chr21:38404640
|
T | C | 268 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.389-931A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404640 | ||||||
| chr21:38404665
|
T | C | 15 | a0001c0001t0001g0202a0001c0001t0001g0255a0001c0001t0001g0258others(12): Show | 15 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.389-956A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404665 | ||||||
| chr21:38404894
|
G | C | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.389-1185C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38404894 | ||||||
| chr21:38405109
|
T | C | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.389-1400A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405109 | ||||||
| chr21:38405298
|
A | G | 285 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.389-1589T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405298 | ||||||
| chr21:38405447
|
G | A | 15 | a0001c0001t0001g0202a0001c0001t0001g0255a0001c0001t0001g0258others(12): Show | 15 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.389-1738C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405447 | ||||||
| chr21:38405530
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.389-1821C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405530 | ||||||
| chr21:38405634
|
G | A | 1 | a0001c0001t0027g0346 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.389-1925C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405634 | ||||||
| chr21:38405806
|
C | T | 36 | a0001c0001t0001g0216a0001c0001t0001g0313a0001c0001t0001g0334others(33): Show | 37 | HG00438.hp2 HG00597.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.389-2097G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405806 | ||||||
| chr21:38405909
|
T | C | 268 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.389-2200A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405909 | ||||||
| chr21:38405943
|
G | A | 17 | a0001c0001t0001g0202a0001c0001t0001g0255a0001c0001t0001g0258others(14): Show | 17 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.389-2234C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405943 | ||||||
| chr21:38405951
|
G | C | 1 | a0001c0001t0006g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389-2242C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405951 | ||||||
| chr21:38405965
|
A | C | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.389-2256T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38405965 | ||||||
| chr21:38406016
|
A | G | 2 | a0001c0001t0001g0259a0001c0001t0011g0279 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.389-2307T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406016 | ||||||
| chr21:38406027
|
T | C | 286 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(283): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.389-2318A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406027 | ||||||
| chr21:38406134
|
G | A | 1 | a0001c0001t0011g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.389-2425C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406134 | ||||||
| chr21:38406141
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.389-2432G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406141 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(3): Show |
1 | a0001c0002t0012g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.389-2455_389-2446d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(4): Show |
14 | a0001c0001t0001g0275a0001c0001t0002g0109a0001c0001t0002g0139others(11): Show | 14 | HG00609.hp1 HG01361.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.389-2456_389-2446d others(13): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(5): Show |
24 | a0001c0001t0001g0107a0001c0001t0002g0123a0001c0001t0002g0140others(21): Show | 24 | HG00408.hp1 HG00558.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.389-2457_389-2446d others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(6): Show |
45 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.389-2458_389-2446d others(15): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(7): Show |
21 | a0001c0001t0001g0231a0001c0001t0001g0250a0001c0001t0002g0111others(18): Show | 21 | HG00642.hp2 HG00735.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.389-2459_389-2446d others(16): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(8): Show |
11 | a0001c0001t0001g0120a0001c0001t0001g0290a0001c0001t0002g0246others(8): Show | 11 | HG01169.hp2 HG01884.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.389-2460_389-2446d others(17): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(9): Show |
20 | a0001c0001t0001g0145a0001c0001t0001g0216a0001c0001t0001g0313others(17): Show | 21 | HG00597.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.389-2461_389-2446d others(18): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(10): Show |
12 | a0001c0001t0002g0081a0001c0001t0002g0168a0001c0001t0002g0225others(9): Show | 12 | HG00438.hp2 HG01978.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.389-2462_389-2446d others(19): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0002g0324 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.389-2464_389-2446d others(21): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
CAAA | C | 6 | a0001c0001t0001g0066a0001c0001t0001g0108a0001c0001t0001g0138others(3): Show | 6 | HG01361.hp1 HG03831.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.389-2448_389-2446d others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
CAAAA | C | 172 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.389-2449_389-2446d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406154
|
CAAAAA | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0207a0001c0001t0001g0217others(4): Show | 7 | HG00609.hp2 HG01346.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.389-2450_389-2446d others(7): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406154 | ||||||
| chr21:38406186
|
G | A | 1 | a0001c0001t0003g0302 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.389-2477C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406186 | ||||||
| chr21:38406197
|
A | G | 4 | a0001c0001t0007g0001a0001c0001t0007g0011a0001c0001t0007g0022others(1): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-2488T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406197 | ||||||
| chr21:38406527
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.389-2818A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406527 | ||||||
| chr21:38406656
|
T | C | 1 | a0001c0001t0002g0333 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.389-2947A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406656 | ||||||
| chr21:38406870
|
A | T | 304 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.389-3161T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406870 | ||||||
| chr21:38406904
|
G | A | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.389-3195C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38406904 | ||||||
| chr21:38407229
|
A | T | 3 | a0001c0001t0001g0259a0001c0001t0011g0232a0001c0001t0011g0279 | 3 | HG02895.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.389-3520T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407229 | ||||||
| chr21:38407267
|
T | C | 1 | a0001c0001t0004g0024 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.389-3558A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407267 | ||||||
| chr21:38407430
|
G | C | 15 | a0001c0001t0001g0275a0001c0001t0002g0146a0001c0001t0002g0296others(12): Show | 15 | HG00323.hp1 HG00609.hp1 HG03669.hp2 others(12): Show |
intron_variant | MODIFIER | c.389-3721C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407430 | ||||||
| chr21:38407465
|
C | T | 304 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.389-3756G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407465 | ||||||
| chr21:38407611
|
G | A | 304 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.389-3902C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407611 | ||||||
| chr21:38407634
|
G | GTATATA | 223 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.389-3931_389-3926d others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(1): Show |
42 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0077others(39): Show | 43 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.389-3933_389-3926d others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0002g0345a0001c0001t0003g0321 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.389-3935_389-3926d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.389-3926_389-3925i others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(13): Show |
9 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0140others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.389-3926_389-3925i others(22): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(15): Show |
8 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0179others(5): Show | 8 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.389-3926_389-3925i others(24): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(17): Show |
4 | a0001c0001t0001g0255a0001c0001t0001g0344a0001c0001t0001g0353others(1): Show | 4 | HG01106.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.389-3926_389-3925i others(26): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(19): Show |
7 | a0001c0001t0001g0258a0001c0001t0001g0261a0001c0001t0001g0264others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-3926_389-3925i others(28): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(21): Show |
3 | a0001c0001t0001g0202a0001c0001t0001g0263a0001c0001t0001g0271 | 3 | HG02723.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.389-3926_389-3925i others(30): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.389-3926_389-3925i others(32): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407634
|
G | GTATGTAT others(31): Show |
1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.389-3926_389-3925i others(40): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407634 | ||||||
| chr21:38407645
|
T | TATATATA others(36): Show |
1 | a0001c0001t0011g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.389-3937_389-3936i others(45): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407645 | ||||||
| chr21:38407646
|
T | A | 303 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.389-3937A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407646 | ||||||
| chr21:38407647
|
T | A | 1 | a0001c0001t0011g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.389-3938A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407647 | ||||||
| chr21:38407647
|
T | TATATATA others(11): Show |
1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.389-3939_389-3938i others(20): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407647 | ||||||
| chr21:38407919
|
AT | A | 57 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0067others(54): Show | 58 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.389-4211delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407919 | ||||||
| chr21:38407992
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.389-4283A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38407992 | ||||||
| chr21:38408020
|
T | C | 6 | a0001c0001t0001g0309a0001c0001t0008g0071a0001c0001t0008g0094others(3): Show | 6 | HG02027.hp2 HG02273.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-4311A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38408020 | ||||||
| chr21:38408024
|
C | T | 17 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.389-4315G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38408024 | ||||||
| chr21:38408203
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.389-4494G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38408203 | ||||||
| chr21:38408254
|
A | G | 305 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.389-4545T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38408254 | ||||||
| chr21:38408630
|
T | C | 304 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.389-4921A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38408630 | ||||||
| chr21:38408661
|
G | A | 1 | a0001c0001t0003g0321 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.389-4952C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38408661 | ||||||
| chr21:38408724
|
A | G | 268 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.389-5015T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38408724 | ||||||
| chr21:38408828
|
G | T | 1 | a0001c0001t0004g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389-5119C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38408828 | ||||||
| chr21:38409210
|
G | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0129a0001c0001t0001g0183others(7): Show | 10 | HG00597.hp1 HG00673.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.389-5501C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409210 | ||||||
| chr21:38409221
|
T | C | 287 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(284): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.389-5512A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409221 | ||||||
| chr21:38409252
|
G | A | 15 | a0001c0001t0001g0275a0001c0001t0002g0146a0001c0001t0002g0296others(12): Show | 15 | HG00323.hp1 HG00609.hp1 HG03669.hp2 others(12): Show |
intron_variant | MODIFIER | c.389-5543C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409252 | ||||||
| chr21:38409254
|
C | T | 18 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(15): Show | 18 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.389-5545G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409254 | ||||||
| chr21:38409273
|
G | C | 287 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(284): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.389-5564C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409273 | ||||||
| chr21:38409433
|
A | C | 102 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.389-5724T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409433 | ||||||
| chr21:38409433
|
A | T | 168 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(165): Show | 169 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.389-5724T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409433 | ||||||
| chr21:38409488
|
T | TA | 128 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(125): Show | 128 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.389-5780dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409488 | ||||||
| chr21:38409488
|
T | TAA | 9 | a0001c0001t0001g0060a0001c0001t0001g0108a0001c0001t0001g0309others(6): Show | 9 | HG02027.hp2 HG02145.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.389-5781_389-5780d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409488 | ||||||
| chr21:38409488
|
T | TAAAA | 16 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0002g0124others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.389-5783_389-5780d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409488 | ||||||
| chr21:38409488
|
TA | T | 8 | a0001c0001t0001g0135a0001c0001t0001g0231a0001c0001t0001g0236others(5): Show | 8 | HG01433.hp1 HG01515.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.389-5780delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409488 | ||||||
| chr21:38409488
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.389-5790_389-5780d others(13): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409488 | ||||||
| chr21:38409517
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.389-5808G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409517 | ||||||
| chr21:38409738
|
G | A | 287 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(284): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.389-6029C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409738 | ||||||
| chr21:38409753
|
G | C | 2 | a0001c0001t0003g0310a0001c0001t0006g0053 | 2 | NA18982.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.389-6044C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409753 | ||||||
| chr21:38409766
|
T | C | 287 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(284): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.389-6057A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409766 | ||||||
| chr21:38409829
|
T | A | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.389-6120A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38409829 | ||||||
| chr21:38410158
|
C | T | 1 | a0001c0001t0001g0351 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.389-6449G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38410158 | ||||||
| chr21:38410317
|
T | C | 2 | a0001c0001t0002g0246a0001c0001t0005g0050 | 2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.389-6608A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38410317 | ||||||
| chr21:38410475
|
G | A | 17 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.389-6766C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38410475 | ||||||
| chr21:38410495
|
C | T | 290 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.389-6786G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38410495 | ||||||
| chr21:38410562
|
T | C | 1 | a0001c0001t0003g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.389-6853A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38410562 | ||||||
| chr21:38410610
|
T | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0156a0001c0001t0001g0267 | 3 | HG01123.hp1 HG01993.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.389-6901A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38410610 | ||||||
| chr21:38410966
|
A | G | 1 | a0001c0003t0010g0251 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.389-7257T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38410966 | ||||||
| chr21:38411049
|
A | G | 288 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(285): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.389-7340T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411049 | ||||||
| chr21:38411289
|
G | T | 1 | a0001c0001t0011g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.389-7580C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411289 | ||||||
| chr21:38411405
|
C | A | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.389-7696G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411405 | ||||||
| chr21:38411406
|
C | T | 106 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.389-7697G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411406 | ||||||
| chr21:38411440
|
G | C | 357 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(354): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.389-7731C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411440 | ||||||
| chr21:38411467
|
G | C | 357 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(354): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.389-7758C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411467 | ||||||
| chr21:38411468
|
T | C | 343 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.389-7759A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411468 | ||||||
| chr21:38411499
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.389-7790C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411499 | ||||||
| chr21:38411587
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.389-7878G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411587 | ||||||
| chr21:38411640
|
A | C | 290 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.389-7931T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411640 | ||||||
| chr21:38411886
|
G | A | 290 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.389-8177C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411886 | ||||||
| chr21:38411898
|
T | G | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.389-8189A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411898 | ||||||
| chr21:38411921
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.389-8212A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38411921 | ||||||
| chr21:38412176
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0004g0051 | 2 | HG01975.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.389-8467G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38412176 | ||||||
| chr21:38412311
|
T | C | 1 | a0001c0001t0008g0071 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.389-8602A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38412311 | ||||||
| chr21:38412818
|
T | C | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.389-9109A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38412818 | ||||||
| chr21:38412830
|
T | C | 94 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.389-9121A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38412830 | ||||||
| chr21:38412885
|
C | T | 14 | a0001c0001t0001g0202a0001c0001t0001g0255a0001c0001t0001g0258others(11): Show | 14 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.389-9176G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38412885 | ||||||
| chr21:38413264
|
G | A | 325 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.389-9555C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38413264 | ||||||
| chr21:38413741
|
T | TGTTA | 290 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.388+9665_388+9668d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38413741 | ||||||
| chr21:38413849
|
T | C | 3 | a0001c0001t0004g0015a0001c0001t0004g0055a0001c0001t0019g0047 | 3 | NA18991.hp2 NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.388+9561A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38413849 | ||||||
| chr21:38414067
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0239 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.388+9343C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38414067 | ||||||
| chr21:38414125
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388+9285A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38414125 | ||||||
| chr21:38414535
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0003g0100 | 2 | HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.388+8875A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38414535 | ||||||
| chr21:38414556
|
T | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0324 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.388+8854A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38414556 | ||||||
| chr21:38414677
|
T | C | 11 | a0001c0001t0001g0096a0001c0001t0001g0237a0001c0001t0001g0240others(8): Show | 11 | HG00280.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.388+8733A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38414677 | ||||||
| chr21:38414691
|
A | G | 112 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(109): Show | 112 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.388+8719T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38414691 | ||||||
| chr21:38414819
|
A | AT | 179 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(176): Show | 180 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.388+8590dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38414819 | ||||||
| chr21:38414819
|
A | ATT | 7 | a0001c0001t0001g0259a0001c0001t0002g0141a0001c0001t0002g0142others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.388+8589_388+8590d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38414819 | ||||||
| chr21:38415005
|
G | A | 275 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.388+8405C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415005 | ||||||
| chr21:38415215
|
C | T | 11 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0140others(8): Show | 11 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.388+8195G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415215 | ||||||
| chr21:38415300
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.388+8110A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415300 | ||||||
| chr21:38415435
|
C | T | 1 | a0001c0001t0021g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.388+7975G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415435 | ||||||
| chr21:38415609
|
G | A | 17 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(14): Show | 17 | HG00639.hp2 HG00735.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.388+7801C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415609 | ||||||
| chr21:38415660
|
T | A | 12 | a0001c0001t0001g0277a0001c0001t0003g0160a0001c0001t0003g0188others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.388+7750A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415660 | ||||||
| chr21:38415669
|
G | A | 15 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(12): Show | 15 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.388+7741C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415669 | ||||||
| chr21:38415701
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0005g0050 | 2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.388+7709G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415701 | ||||||
| chr21:38415972
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.388+7438G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38415972 | ||||||
| chr21:38416166
|
A | G | 1 | a0001c0001t0002g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.388+7244T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38416166 | ||||||
| chr21:38416292
|
C | T | 1 | a0001c0001t0007g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.388+7118G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38416292 | ||||||
| chr21:38416311
|
T | C | 1 | a0001c0001t0007g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.388+7099A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38416311 | ||||||
| chr21:38416487
|
C | T | 1 | a0001c0001t0009g0144 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.388+6923G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38416487 | ||||||
| chr21:38416581
|
A | C | 58 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0067others(55): Show | 59 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.388+6829T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38416581 | ||||||
| chr21:38416796
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.388+6614C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38416796 | ||||||
| chr21:38416882
|
G | A | 158 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(155): Show | 159 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.388+6528C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38416882 | ||||||
| chr21:38416883
|
C | T | 2 | a0001c0001t0011g0205a0001c0001t0011g0320 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.388+6527G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38416883 | ||||||
| chr21:38417238
|
A | G | 325 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(322): Show | 327 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.388+6172T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38417238 | ||||||
| chr21:38417516
|
C | T | 96 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.388+5894G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38417516 | ||||||
| chr21:38417555
|
G | A | 1 | a0001c0001t0004g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.388+5855C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38417555 | ||||||
| chr21:38417617
|
C | T | 5 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0179others(2): Show | 5 | HG02622.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+5793G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38417617 | ||||||
| chr21:38417684
|
G | C | 113 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.388+5726C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38417684 | ||||||
| chr21:38417815
|
TA | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0119a0001c0001t0001g0193others(2): Show | 5 | HG00558.hp1 HG02129.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+5594delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38417815 | ||||||
| chr21:38417879
|
A | G | 5 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0179others(2): Show | 5 | HG02622.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+5531T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38417879 | ||||||
| chr21:38418025
|
T | A | 7 | a0001c0001t0001g0127a0001c0001t0001g0143a0001c0001t0001g0186others(4): Show | 7 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.388+5385A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418025 | ||||||
| chr21:38418144
|
G | T | 5 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0179others(2): Show | 5 | HG02622.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+5266C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418144 | ||||||
| chr21:38418162
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388+5248T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418162 | ||||||
| chr21:38418270
|
A | AGT | 9 | a0001c0001t0001g0066a0001c0001t0001g0119a0001c0001t0001g0193others(6): Show | 9 | HG00558.hp1 HG02129.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+5138_388+5139d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418270
|
A | AGTGT | 55 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0073others(52): Show | 56 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.388+5136_388+5139d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418270
|
A | AGTGTGT | 52 | a0001c0001t0001g0120a0001c0001t0001g0135a0001c0001t0001g0159others(49): Show | 52 | HG00099.hp1 HG00558.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.388+5134_388+5139d others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418270
|
A | AGTGTGTG others(1): Show |
33 | a0001c0001t0001g0149a0001c0001t0001g0158a0001c0001t0001g0202others(30): Show | 33 | HG00280.hp2 HG00639.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.388+5132_388+5139d others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418270
|
A | AGTGTGTG others(3): Show |
28 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(25): Show | 28 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.388+5130_388+5139d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418270
|
A | AGTGTGTG others(5): Show |
34 | a0001c0001t0001g0090a0001c0001t0001g0099a0001c0001t0001g0107others(31): Show | 34 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.388+5128_388+5139d others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418270
|
A | AGTGTGTG others(7): Show |
20 | a0001c0001t0001g0283a0001c0001t0002g0121a0001c0001t0002g0122others(17): Show | 20 | HG00735.hp1 HG01243.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.388+5126_388+5139d others(16): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418270
|
A | AGTGTGTG others(9): Show |
11 | a0001c0001t0002g0081a0001c0001t0002g0295a0001c0001t0002g0355others(8): Show | 12 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.388+5124_388+5139d others(18): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418270
|
A | AGTGTGTG others(11): Show |
1 | a0001c0001t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.388+5122_388+5139d others(20): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418270 | ||||||
| chr21:38418281
|
G | GTGTGTC | 98 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(95): Show | 98 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.388+5128_388+5129i others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418281 | ||||||
| chr21:38418312
|
G | T | 1 | a0001c0001t0004g0020 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.388+5098C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418312 | ||||||
| chr21:38418364
|
G | A | 2 | a0001c0001t0011g0205a0001c0001t0011g0320 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.388+5046C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418364 | ||||||
| chr21:38418496
|
G | A | 1 | a0001c0001t0021g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.388+4914C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418496 | ||||||
| chr21:38418596
|
G | A | 17 | a0001c0001t0001g0275a0001c0001t0001g0311a0001c0001t0002g0087others(14): Show | 17 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.388+4814C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418596 | ||||||
| chr21:38418698
|
G | A | 1 | a0001c0001t0006g0035 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.388+4712C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418698 | ||||||
| chr21:38418843
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0152 | 3 | NA18963.hp2 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.388+4567G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418843 | ||||||
| chr21:38418881
|
C | T | 1 | a0001c0001t0010g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.388+4529G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418881 | ||||||
| chr21:38418914
|
C | T | 17 | a0001c0001t0001g0275a0001c0001t0001g0311a0001c0001t0002g0087others(14): Show | 17 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.388+4496G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418914 | ||||||
| chr21:38418927
|
CA | C | 26 | a0001c0001t0001g0239a0001c0001t0001g0275a0001c0001t0001g0311others(23): Show | 26 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.388+4482delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418927 | ||||||
| chr21:38418927
|
CAA | C | 141 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(138): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.388+4481_388+4482d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418927 | ||||||
| chr21:38418927
|
CAAA | C | 152 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(149): Show | 153 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.388+4480_388+4482d others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418927 | ||||||
| chr21:38418927
|
CAAAA | C | 9 | a0001c0001t0001g0058a0001c0001t0001g0213a0001c0001t0001g0287others(6): Show | 9 | HG02572.hp1 HG02622.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+4479_388+4482d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418927 | ||||||
| chr21:38418938
|
AAAAAAAA others(6): Show |
A | 7 | a0001c0001t0001g0259a0001c0001t0002g0141a0001c0001t0002g0142others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.388+4459_388+4471d others(15): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418938 | ||||||
| chr21:38418947
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0002g0265 | 2 | HG03041.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.388+4463T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418947 | ||||||
| chr21:38418949
|
A | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0176 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.388+4461T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418949 | ||||||
| chr21:38418961
|
A | G | 1 | a0001c0001t0002g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.388+4449T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38418961 | ||||||
| chr21:38419018
|
G | A | 17 | a0001c0001t0001g0275a0001c0001t0001g0311a0001c0001t0002g0087others(14): Show | 17 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.388+4392C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419018 | ||||||
| chr21:38419252
|
A | G | 2 | a0001c0001t0002g0109a0001c0001t0005g0004 | 2 | HG02080.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.388+4158T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419252 | ||||||
| chr21:38419294
|
T | C | 343 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(340): Show | 345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.388+4116A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419294 | ||||||
| chr21:38419470
|
C | G | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.388+3940G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419470 | ||||||
| chr21:38419516
|
T | TAC | 309 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(306): Show | 311 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.388+3892_388+3893d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419516 | ||||||
| chr21:38419558
|
ACT | A | 17 | a0001c0001t0001g0311a0001c0001t0002g0146a0001c0001t0002g0265others(14): Show | 17 | HG00609.hp1 HG02258.hp2 HG03041.hp1 others(14): Show |
intron_variant | MODIFIER | c.388+3850_388+3851d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419558 | ||||||
| chr21:38419699
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.388+3711T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419699 | ||||||
| chr21:38419757
|
CT | C | 153 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(150): Show | 154 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.388+3652delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419757 | ||||||
| chr21:38419939
|
C | T | 208 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(205): Show | 208 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.388+3471G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419939 | ||||||
| chr21:38419988
|
G | A | 1 | a0001c0001t0002g0347 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.388+3422C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38419988 | ||||||
| chr21:38420003
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.388+3407A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420003 | ||||||
| chr21:38420031
|
G | GT | 42 | a0001c0001t0001g0067a0001c0001t0001g0098a0001c0001t0001g0099others(39): Show | 42 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.388+3378dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420031 | ||||||
| chr21:38420031
|
G | GTT | 63 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.388+3377_388+3378d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420031 | ||||||
| chr21:38420047
|
C | T | 116 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0076others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.388+3363G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420047 | ||||||
| chr21:38420083
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.388+3327T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420083 | ||||||
| chr21:38420288
|
C | CTG | 34 | a0001c0001t0001g0076a0001c0001t0001g0261a0001c0001t0001g0334others(31): Show | 34 | HG00438.hp2 HG01346.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.388+3120_388+3121d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420288 | ||||||
| chr21:38420303
|
CGT | C | 158 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(155): Show | 160 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.388+3105_388+3106d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420303 | ||||||
| chr21:38420519
|
C | T | 167 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0066others(164): Show | 169 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.388+2891G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420519 | ||||||
| chr21:38420592
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.388+2818A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420592 | ||||||
| chr21:38420679
|
A | G | 66 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.388+2731T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420679 | ||||||
| chr21:38420721
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.388+2689T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420721 | ||||||
| chr21:38420825
|
A | T | 8 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+2585T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420825 | ||||||
| chr21:38420854
|
G | T | 8 | a0001c0001t0001g0135a0001c0001t0001g0319a0001c0001t0002g0307others(5): Show | 8 | HG00558.hp2 HG02165.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.388+2556C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420854 | ||||||
| chr21:38420865
|
T | C | 7 | a0001c0001t0001g0259a0001c0001t0002g0141a0001c0001t0002g0142others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.388+2545A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420865 | ||||||
| chr21:38420900
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.388+2510A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420900 | ||||||
| chr21:38420940
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.388+2470G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38420940 | ||||||
| chr21:38421075
|
T | G | 2 | a0001c0001t0001g0070a0001c0001t0004g0021 | 2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.388+2335A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421075 | ||||||
| chr21:38421257
|
T | A | 8 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+2153A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421257 | ||||||
| chr21:38421261
|
G | T | 16 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(13): Show | 16 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.388+2149C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421261 | ||||||
| chr21:38421262
|
A | T | 16 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(13): Show | 16 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.388+2148T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421262 | ||||||
| chr21:38421272
|
C | A | 1 | a0001c0001t0027g0346 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.388+2138G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421272 | ||||||
| chr21:38421355
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.388+2055A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421355 | ||||||
| chr21:38421373
|
G | A | 1 | a0001c0001t0004g0043 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.388+2037C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421373 | ||||||
| chr21:38421385
|
C | T | 2 | a0001c0001t0003g0195a0001c0001t0003g0270 | 2 | HG01515.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.388+2025G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421385 | ||||||
| chr21:38421947
|
G | C | 1 | a0001c0001t0011g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.388+1463C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421947 | ||||||
| chr21:38421981
|
G | C | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.388+1429C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38421981 | ||||||
| chr21:38422019
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.388+1391C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422019 | ||||||
| chr21:38422136
|
C | T | 123 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(120): Show | 123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.388+1274G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422136 | ||||||
| chr21:38422259
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.388+1151G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422259 | ||||||
| chr21:38422306
|
G | A | 105 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0076others(102): Show | 106 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.388+1104C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422306 | ||||||
| chr21:38422509
|
C | G | 8 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+901G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422509 | ||||||
| chr21:38422520
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.388+890C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422520 | ||||||
| chr21:38422579
|
G | A | 105 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0076others(102): Show | 106 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.388+831C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422579 | ||||||
| chr21:38422761
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.388+649T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422761 | ||||||
| chr21:38422766
|
A | G | 1 | a0001c0001t0003g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.388+644T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422766 | ||||||
| chr21:38422834
|
A | G | 16 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(13): Show | 16 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.388+576T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422834 | ||||||
| chr21:38422840
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.388+570A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422840 | ||||||
| chr21:38422872
|
G | T | 8 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+538C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422872 | ||||||
| chr21:38422901
|
T | C | 8 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+509A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422901 | ||||||
| chr21:38422913
|
T | G | 55 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(52): Show | 56 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.388+497A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422913 | ||||||
| chr21:38422958
|
T | G | 345 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(342): Show | 347 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.388+452A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38422958 | ||||||
| chr21:38423084
|
A | AGT | 40 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0074others(37): Show | 40 | HG00280.hp1 HG00408.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.388+324_388+325dup others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
A | AGTGT | 58 | a0001c0001t0001g0107a0001c0001t0001g0120a0001c0001t0001g0127others(55): Show | 58 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.388+322_388+325dup others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
A | AGTGTGT | 37 | a0001c0001t0001g0059a0001c0001t0001g0076a0001c0001t0001g0086others(34): Show | 38 | HG00323.hp1 HG00438.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.388+320_388+325dup others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
A | AGTGTGTG others(1): Show |
4 | a0001c0001t0002g0168a0001c0001t0002g0180a0001c0001t0003g0056others(1): Show | 4 | HG02074.hp1 HG04204.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+318_388+325dup others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
A | AGTGTGTG others(3): Show |
10 | a0001c0001t0001g0073a0001c0001t0001g0159a0001c0001t0001g0261others(7): Show | 10 | HG00738.hp2 HG01081.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+316_388+325dup others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
AGT | A | 17 | a0001c0001t0001g0058a0001c0001t0001g0103a0001c0001t0001g0114others(14): Show | 17 | HG00099.hp2 HG00597.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.388+324_388+325del others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
AGTGT | A | 12 | a0001c0001t0001g0097a0001c0001t0001g0200a0001c0001t0001g0215others(9): Show | 12 | HG00738.hp1 HG01106.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.388+322_388+325del others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
AGTGTGT | A | 15 | a0001c0001t0001g0259a0001c0001t0001g0275a0001c0001t0001g0291others(12): Show | 15 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.388+320_388+325del others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
AGTGTGTG others(3): Show |
A | 3 | a0001c0001t0002g0265a0001c0001t0002g0349a0001c0001t0002g0350 | 3 | HG03041.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.388+316_388+325del others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423084
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.388+314_388+325del others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423084 | ||||||
| chr21:38423115
|
G | A | 51 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(48): Show | 52 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.388+295C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423115 | ||||||
| chr21:38423234
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.388+176G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423234 | ||||||
| chr21:38423280
|
T | G | 125 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(122): Show | 125 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.388+130A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423280 | ||||||
| chr21:38423311
|
G | A | 1 | a0001c0001t0024g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.388+99C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 3/9 | chr21 | 38423311 | ||||||
| chr21:38423637
|
G | T | 1 | a0001c0001t0002g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.237-76C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38423637 | ||||||
| chr21:38423762
|
C | A | 1 | a0001c0001t0009g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.237-201G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38423762 | ||||||
| chr21:38423981
|
A | AAAAAG | 199 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(196): Show | 200 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.237-425_237-421dup others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38423981 | ||||||
| chr21:38424009
|
G | A | 4 | a0001c0001t0002g0254a0001c0001t0002g0265a0001c0001t0002g0349others(1): Show | 4 | HG02559.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-448C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424009 | ||||||
| chr21:38424057
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.237-496G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424057 | ||||||
| chr21:38424178
|
AGAGCTC | A | 15 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0143others(12): Show | 15 | HG00642.hp1 HG00673.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.237-623_237-618del others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424178 | ||||||
| chr21:38424180
|
A | AGC | 9 | a0001c0001t0001g0061a0001c0001t0001g0187a0001c0001t0002g0140others(6): Show | 9 | HG02083.hp1 HG02135.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-621_237-620dup others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424180 | ||||||
| chr21:38424181
|
G | GCGCTCT | 5 | a0001c0001t0001g0312a0001c0001t0002g0121a0001c0001t0002g0122others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-621_237-620ins others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
G | GCGCTCTC others(7): Show |
1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.237-621_237-620ins others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
G | GCT | 28 | a0001c0001t0001g0127a0001c0001t0001g0158a0001c0001t0001g0255others(25): Show | 28 | HG01981.hp1 HG02015.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.237-622_237-621dup others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
G | GCTCT | 22 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0193others(19): Show | 22 | HG00639.hp2 HG01106.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.237-621_237-620ins others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
G | GCTCTCT | 3 | a0001c0001t0001g0076a0001c0001t0002g0166a0001c0001t0011g0205 | 3 | HG01346.hp1 NA19043.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.237-621_237-620ins others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
GCT | G | 27 | a0001c0001t0001g0104a0001c0001t0001g0108a0001c0001t0001g0165others(24): Show | 27 | HG00438.hp2 HG00738.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.237-622_237-621del others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
GCTCGAGC others(1): Show |
G | 17 | a0001c0001t0001g0079a0001c0001t0001g0106a0001c0001t0001g0107others(14): Show | 17 | HG00597.hp2 HG00639.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.237-628_237-621del others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
GCTCGAGC others(3): Show |
G | 16 | a0001c0001t0001g0211a0001c0001t0001g0267a0001c0001t0001g0291others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-630_237-621del others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
GCTCGAGC others(9): Show |
G | 3 | a0001c0001t0002g0265a0001c0001t0002g0349a0001c0001t0002g0350 | 3 | HG03041.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-636_237-621del others(16): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424181
|
GCTCGAGC others(21): Show |
G | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.237-648_237-621del others(28): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424181 | ||||||
| chr21:38424182
|
CTCGA | C | 54 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0080others(51): Show | 54 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.237-625_237-622del others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424182 | ||||||
| chr21:38424183
|
T | G | 15 | a0001c0001t0001g0058a0001c0001t0001g0105a0001c0001t0001g0184others(12): Show | 15 | HG02273.hp2 HG02451.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-622A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424183 | ||||||
| chr21:38424183
|
TCGAG | T | 38 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0098others(35): Show | 39 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.237-626_237-623del others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424183 | ||||||
| chr21:38424184
|
CGA | C | 44 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0096others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.237-625_237-624del others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424184 | ||||||
| chr21:38424185
|
G | T | 131 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(128): Show | 132 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.237-624C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424185 | ||||||
| chr21:38424186
|
A | C | 158 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(155): Show | 159 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(156): Show |
intron_variant | MODIFIER | c.237-625T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424186 | ||||||
| chr21:38424187
|
G | T | 202 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(199): Show | 203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.237-626C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424187 | ||||||
| chr21:38424189
|
T | G | 10 | a0001c0001t0001g0064a0001c0001t0001g0153a0001c0001t0001g0156others(7): Show | 10 | HG00642.hp1 HG01069.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-628A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424189 | ||||||
| chr21:38424191
|
T | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0216a0001c0001t0001g0311 | 3 | HG00597.hp2 HG02602.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.237-630A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424191 | ||||||
| chr21:38424193
|
T | G | 2 | a0001c0001t0001g0267a0001c0001t0003g0302 | 2 | HG01993.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.237-632A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424193 | ||||||
| chr21:38424211
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.237-650A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424211 | ||||||
| chr21:38424381
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0159 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.237-820C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424381 | ||||||
| chr21:38424445
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.237-884G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424445 | ||||||
| chr21:38424459
|
G | A | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.237-898C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424459 | ||||||
| chr21:38424471
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.237-910A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424471 | ||||||
| chr21:38424614
|
C | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0143a0001c0001t0001g0238others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-1053G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424614 | ||||||
| chr21:38424676
|
C | T | 113 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0066others(110): Show | 115 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.237-1115G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424676 | ||||||
| chr21:38424923
|
C | T | 3 | a0001c0001t0002g0265a0001c0001t0002g0349a0001c0001t0002g0350 | 3 | HG03041.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-1362G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38424923 | ||||||
| chr21:38425114
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.237-1553A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425114 | ||||||
| chr21:38425209
|
C | G | 1 | a0001c0001t0002g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.237-1648G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425209 | ||||||
| chr21:38425227
|
T | C | 24 | a0001c0001t0001g0076a0001c0001t0001g0334a0001c0001t0002g0078others(21): Show | 24 | HG01346.hp1 HG01496.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.237-1666A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425227 | ||||||
| chr21:38425239
|
T | C | 289 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(286): Show | 291 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.237-1678A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425239 | ||||||
| chr21:38425240
|
G | A | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237-1679C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425240 | ||||||
| chr21:38425382
|
T | A | 2 | a0001c0001t0002g0349a0001c0001t0002g0350 | 2 | NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-1821A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425382 | ||||||
| chr21:38425467
|
A | C | 1 | a0001c0001t0016g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.237-1906T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425467 | ||||||
| chr21:38425510
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.237-1949C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425510 | ||||||
| chr21:38425511
|
T | C | 1 | a0001c0001t0011g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-1950A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425511 | ||||||
| chr21:38425568
|
T | C | 1 | a0001c0001t0009g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.237-2007A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425568 | ||||||
| chr21:38425685
|
T | A | 16 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(13): Show | 16 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.237-2124A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425685 | ||||||
| chr21:38425828
|
A | G | 6 | a0001c0001t0001g0261a0001c0001t0002g0123a0001c0001t0002g0124others(3): Show | 6 | HG02572.hp2 HG02622.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-2267T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425828 | ||||||
| chr21:38425842
|
C | A | 243 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(240): Show | 245 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.237-2281G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425842 | ||||||
| chr21:38425858
|
G | A | 60 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0120others(57): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.237-2297C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425858 | ||||||
| chr21:38425859
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.237-2298C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38425859 | ||||||
| chr21:38426047
|
A | G | 2 | a0001c0001t0003g0262a0001c0001t0003g0272 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.237-2486T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426047 | ||||||
| chr21:38426555
|
G | A | 15 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(12): Show | 15 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.237-2994C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426555 | ||||||
| chr21:38426571
|
C | A | 1 | a0001c0001t0004g0020 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.237-3010G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426571 | ||||||
| chr21:38426668
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.237-3107G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426668 | ||||||
| chr21:38426718
|
G | T | 1 | a0001c0001t0002g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.237-3157C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426718 | ||||||
| chr21:38426769
|
TA | T | 60 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0120others(57): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.237-3209delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426769 | ||||||
| chr21:38426807
|
G | A | 3 | a0001c0001t0002g0265a0001c0001t0003g0221a0001c0001t0003g0298 | 3 | HG03041.hp1 NA18939.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.237-3246C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426807 | ||||||
| chr21:38426812
|
C | T | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.237-3251G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426812 | ||||||
| chr21:38426822
|
C | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0187a0001c0001t0001g0312others(2): Show | 5 | HG00735.hp1 HG02083.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-3261G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426822 | ||||||
| chr21:38426828
|
G | A | 1 | a0001c0001t0016g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.237-3267C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426828 | ||||||
| chr21:38426830
|
T | G | 5 | a0001c0001t0002g0140a0001c0001t0002g0182a0001c0001t0002g0243others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-3269A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426830 | ||||||
| chr21:38426879
|
A | G | 343 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(340): Show | 345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.237-3318T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426879 | ||||||
| chr21:38426886
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.237-3325G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426886 | ||||||
| chr21:38426914
|
G | A | 52 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(49): Show | 53 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.237-3353C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426914 | ||||||
| chr21:38426920
|
G | T | 1 | a0001c0001t0002g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.237-3359C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426920 | ||||||
| chr21:38426922
|
C | T | 3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0347 | 3 | HG02145.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.237-3361G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426922 | ||||||
| chr21:38426930
|
C | CA | 301 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(298): Show | 303 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.237-3370dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426930 | ||||||
| chr21:38426942
|
G | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0143a0001c0001t0001g0238others(2): Show | 5 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-3381C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38426942 | ||||||
| chr21:38427092
|
G | A | 59 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0120others(56): Show | 60 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.237-3531C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427092 | ||||||
| chr21:38427169
|
G | A | 42 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.237-3608C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427169 | ||||||
| chr21:38427204
|
A | C | 127 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(124): Show | 127 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.237-3643T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427204 | ||||||
| chr21:38427231
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.237-3670G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427231 | ||||||
| chr21:38427232
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.237-3671C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427232 | ||||||
| chr21:38427264
|
G | C | 169 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.237-3703C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427264 | ||||||
| chr21:38427355
|
G | A | 1 | a0001c0001t0002g0260 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.237-3794C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427355 | ||||||
| chr21:38427434
|
G | A | 3 | a0001c0001t0002g0087a0001c0001t0002g0235a0001c0001t0010g0084 | 3 | HG00639.hp1 HG03704.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.237-3873C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427434 | ||||||
| chr21:38427543
|
C | G | 8 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-3982G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427543 | ||||||
| chr21:38427592
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.237-4031G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427592 | ||||||
| chr21:38427616
|
T | C | 182 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(179): Show | 183 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.237-4055A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427616 | ||||||
| chr21:38427754
|
G | C | 2 | a0001c0001t0001g0313a0001c0001t0004g0025 | 2 | NA18952.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.237-4193C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427754 | ||||||
| chr21:38427903
|
G | A | 1 | a0001c0001t0001g0357 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.237-4342C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427903 | ||||||
| chr21:38427925
|
G | A | 16 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(13): Show | 16 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.237-4364C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38427925 | ||||||
| chr21:38428040
|
G | A | 1 | a0001c0001t0004g0007 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.237-4479C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428040 | ||||||
| chr21:38428174
|
G | C | 285 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(282): Show | 287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.237-4613C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428174 | ||||||
| chr21:38428180
|
C | CA | 183 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(180): Show | 184 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.237-4620dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428180 | ||||||
| chr21:38428180
|
C | CAA | 43 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.237-4621_237-4620d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428180 | ||||||
| chr21:38428287
|
G | A | 1 | a0001c0001t0002g0317 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.237-4726C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428287 | ||||||
| chr21:38428304
|
C | T | 59 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0120others(56): Show | 60 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.237-4743G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428304 | ||||||
| chr21:38428395
|
C | T | 3 | a0001c0001t0003g0131a0001c0001t0003g0221a0001c0001t0003g0298 | 3 | HG02132.hp2 NA18939.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.237-4834G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428395 | ||||||
| chr21:38428427
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.237-4866G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428427 | ||||||
| chr21:38428428
|
G | A | 1 | a0001c0001t0002g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.237-4867C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428428 | ||||||
| chr21:38428622
|
C | T | 1 | a0001c0001t0004g0026 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.237-5061G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428622 | ||||||
| chr21:38428662
|
C | A | 1 | a0001c0001t0004g0025 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.237-5101G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428662 | ||||||
| chr21:38428666
|
C | T | 54 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(51): Show | 55 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.237-5105G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428666 | ||||||
| chr21:38428775
|
T | C | 128 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(125): Show | 128 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.237-5214A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428775 | ||||||
| chr21:38428831
|
G | A | 1 | a0001c0001t0011g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-5270C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428831 | ||||||
| chr21:38428885
|
T | C | 55 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(52): Show | 56 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.237-5324A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428885 | ||||||
| chr21:38428887
|
T | C | 1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.237-5326A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428887 | ||||||
| chr21:38428939
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.237-5378G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38428939 | ||||||
| chr21:38429045
|
C | T | 59 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0120others(56): Show | 60 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.237-5484G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429045 | ||||||
| chr21:38429048
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0004g0024a0001c0001t0004g0031 | 3 | HG00323.hp2 HG01496.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.237-5487G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429048 | ||||||
| chr21:38429137
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.237-5576A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429137 | ||||||
| chr21:38429156
|
G | A | 2 | a0001c0001t0011g0205a0001c0001t0011g0320 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.237-5595C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429156 | ||||||
| chr21:38429164
|
G | A | 1 | a0001c0001t0011g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-5603C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429164 | ||||||
| chr21:38429256
|
G | GTA | 55 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(52): Show | 56 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.237-5697_237-5696d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429256 | ||||||
| chr21:38429299
|
C | CATATGTA others(19): Show |
1 | a0001c0001t0002g0350 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.237-5764_237-5739d others(28): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429299 | ||||||
| chr21:38429324
|
A | G | 1 | a0001c0001t0006g0035 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.237-5763T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429324 | ||||||
| chr21:38429361
|
T | C | 1 | a0001c0001t0005g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.237-5800A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429361 | ||||||
| chr21:38429368
|
T | C | 42 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.237-5807A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429368 | ||||||
| chr21:38429382
|
T | C | 125 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(122): Show | 125 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.237-5821A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429382 | ||||||
| chr21:38429387
|
GTACACAT others(1): Show |
G | 167 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(164): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.237-5834_237-5827d others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429387 | ||||||
| chr21:38429393
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.237-5832T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429393 | ||||||
| chr21:38429395
|
A | ATACACAT others(1): Show |
63 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(60): Show | 64 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.237-5842_237-5835d others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429395 | ||||||
| chr21:38429408
|
T | C | 4 | a0001c0001t0001g0190a0001c0001t0001g0211a0001c0001t0003g0335others(1): Show | 4 | HG01975.hp1 HG02015.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5847A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429408 | ||||||
| chr21:38429409
|
A | G | 7 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-5848T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429409 | ||||||
| chr21:38429420
|
A | T | 116 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0066others(113): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.237-5859T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429420 | ||||||
| chr21:38429423
|
ATG | A | 60 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(57): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.237-5864_237-5863d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429423 | ||||||
| chr21:38429439
|
ATACACGT others(1): Show |
A | 125 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(122): Show | 125 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.237-5886_237-5879d others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429439 | ||||||
| chr21:38429444
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.237-5883G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429444 | ||||||
| chr21:38429444
|
C | T | 60 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(57): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.237-5883G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429444 | ||||||
| chr21:38429445
|
G | A | 2 | a0001c0001t0002g0349a0001c0001t0002g0350 | 2 | NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-5884C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429445 | ||||||
| chr21:38429458
|
CAT | C | 3 | a0001c0001t0002g0265a0001c0001t0002g0349a0001c0001t0002g0350 | 3 | HG03041.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-5899_237-5898d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429458 | ||||||
| chr21:38429460
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.237-5899A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429460 | ||||||
| chr21:38429464
|
C | T | 1 | a0001c0001t0019g0047 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.237-5903G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429464 | ||||||
| chr21:38429466
|
CAT | C | 35 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0079others(32): Show | 35 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.237-5907_237-5906d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429466 | ||||||
| chr21:38429466
|
CATATGTG others(71): Show |
C | 1 | a0001c0001t0019g0047 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.237-5983_237-5906d others(80): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429466 | ||||||
| chr21:38429470
|
T | C | 66 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.237-5909A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429470 | ||||||
| chr21:38429477
|
ATACATGT others(111): Show |
A | 1 | a0001c0001t0001g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.237-6034_237-5917d others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429477 | ||||||
| chr21:38429478
|
TACATGTA others(81): Show |
T | 52 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(49): Show | 53 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.237-6005_237-5918d others(90): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429478 | ||||||
| chr21:38429486
|
T | G | 1 | a0001c0001t0002g0333 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.237-5925A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429486 | ||||||
| chr21:38429487
|
G | A | 289 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(286): Show | 290 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.237-5926C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429487 | ||||||
| chr21:38429494
|
T | C | 42 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.237-5933A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429494 | ||||||
| chr21:38429496
|
CAT | C | 6 | a0001c0001t0001g0261a0001c0001t0002g0123a0001c0001t0002g0124others(3): Show | 6 | HG02572.hp2 HG02622.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-5937_237-5936d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429496 | ||||||
| chr21:38429499
|
A | G | 45 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.237-5938T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429499 | ||||||
| chr21:38429502
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0264a0001c0001t0002g0254 | 3 | HG02559.hp2 HG02698.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.237-5941A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429502 | ||||||
| chr21:38429504
|
CAT | C | 60 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(57): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.237-5945_237-5944d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429504 | ||||||
| chr21:38429506
|
T | G | 20 | a0001c0001t0001g0076a0001c0001t0001g0334a0001c0001t0002g0078others(17): Show | 20 | HG01346.hp1 HG01496.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.237-5945A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429506 | ||||||
| chr21:38429511
|
G | GTATATAC others(153): Show |
1 | a0001c0001t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.237-5951_237-5950i others(162): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429511 | ||||||
| chr21:38429511
|
G | GTATATAC others(153): Show |
9 | a0001c0001t0001g0158a0001c0001t0001g0258a0001c0001t0001g0263others(6): Show | 9 | HG00639.hp2 HG01106.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-5951_237-5950i others(162): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429511 | ||||||
| chr21:38429511
|
G | GTATATAC others(193): Show |
4 | a0001c0001t0001g0264a0001c0001t0001g0286a0001c0001t0030g0256others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-5951_237-5950i others(202): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429511 | ||||||
| chr21:38429511
|
GTATATAC others(81): Show |
G | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.237-6038_237-5951d others(90): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429511 | ||||||
| chr21:38429513
|
A | C | 1 | a0001c0001t0002g0126 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.237-5952T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429513 | ||||||
| chr21:38429513
|
A | G | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.237-5952T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429513 | ||||||
| chr21:38429515
|
ATACATGT others(33): Show |
A | 3 | a0001c0001t0002g0350a0001c0001t0011g0205a0001c0001t0011g0320 | 3 | HG02572.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-5994_237-5955d others(42): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429515 | ||||||
| chr21:38429517
|
A | G | 1 | a0001c0001t0002g0245 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.237-5956T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429517 | ||||||
| chr21:38429525
|
G | A | 285 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0064others(282): Show | 286 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.237-5964C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429525 | ||||||
| chr21:38429540
|
T | C | 228 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0064others(225): Show | 229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.237-5979A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429540 | ||||||
| chr21:38429544
|
TATGTGTA others(47): Show |
T | 1 | a0001c0001t0001g0268 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.237-6037_237-5984d others(56): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429544 | ||||||
| chr21:38429549
|
GTATATGT others(43): Show |
G | 185 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0064others(182): Show | 186 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.237-6038_237-5989d others(52): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429549 | ||||||
| chr21:38429555
|
G | A | 55 | a0001c0001t0001g0076a0001c0001t0001g0158a0001c0001t0001g0202others(52): Show | 55 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.237-5994C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429555 | ||||||
| chr21:38429563
|
A | G | 1 | a0001c0001t0011g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237-6002T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429563 | ||||||
| chr21:38429578
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.237-6017A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429578 | ||||||
| chr21:38429580
|
T | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(6): Show | 9 | HG01074.hp2 HG01081.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.237-6019A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429580 | ||||||
| chr21:38429585
|
ATG | A | 8 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-6026_237-6025d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429585 | ||||||
| chr21:38429589
|
GTATATGT others(3): Show |
G | 2 | a0001c0001t0002g0350a0001c0001t0019g0047 | 2 | NA18991.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.237-6038_237-6029d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429589 | ||||||
| chr21:38429593
|
ATG | A | 34 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0112others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.237-6034_237-6033d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429593 | ||||||
| chr21:38429595
|
G | A | 108 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(105): Show | 109 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.237-6034C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429595 | ||||||
| chr21:38429595
|
G | GTACATGT others(71): Show |
7 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(4): Show | 7 | HG01074.hp2 HG01081.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-6035_237-6034i others(80): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429595 | ||||||
| chr21:38429599
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.237-6038T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429599 | ||||||
| chr21:38429600
|
T | C | 52 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(49): Show | 53 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.237-6039A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429600 | ||||||
| chr21:38429603
|
A | G | 1 | a0001c0001t0001g0311 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.237-6042T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429603 | ||||||
| chr21:38429612
|
T | A | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.237-6051A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429612 | ||||||
| chr21:38429626
|
T | C | 125 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(122): Show | 125 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.237-6065A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429626 | ||||||
| chr21:38429631
|
A | G | 52 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(49): Show | 53 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.237-6070T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429631 | ||||||
| chr21:38429632
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.237-6071A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429632 | ||||||
| chr21:38429635
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.237-6074T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429635 | ||||||
| chr21:38429641
|
G | GTATACAC others(33): Show |
8 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-6081_237-6080i others(42): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429641 | ||||||
| chr21:38429647
|
A | G | 1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.237-6086T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429647 | ||||||
| chr21:38429652
|
T | A | 256 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(253): Show | 258 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.237-6091A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429652 | ||||||
| chr21:38429652
|
T | TACATATA others(33): Show |
31 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0112others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.237-6092_237-6091i others(42): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429652 | ||||||
| chr21:38429652
|
T | TACATATA others(73): Show |
3 | a0001c0001t0001g0231a0001c0001t0001g0236a0001c0001t0001g0250 | 3 | HG01433.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.237-6092_237-6091i others(82): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429652 | ||||||
| chr21:38429662
|
CAT | C | 52 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(49): Show | 53 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.237-6103_237-6102d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429662 | ||||||
| chr21:38429665
|
A | G | 67 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(64): Show | 68 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.237-6104T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429665 | ||||||
| chr21:38429667
|
A | ATGTATAT others(153): Show |
2 | a0001c0001t0001g0255a0001c0001t0001g0344 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.237-6107_237-6106i others(162): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429667 | ||||||
| chr21:38429667
|
A | G | 14 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0258others(11): Show | 14 | HG00639.hp2 HG01106.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.237-6106T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429667 | ||||||
| chr21:38429685
|
A | G | 17 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0211others(14): Show | 17 | HG00639.hp2 HG01106.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-6124T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429685 | ||||||
| chr21:38429705
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.237-6144C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429705 | ||||||
| chr21:38429710
|
TGC | T | 67 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(64): Show | 68 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.237-6151_237-6150d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429710 | ||||||
| chr21:38429712
|
C | T | 222 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(219): Show | 223 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.237-6151G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429712 | ||||||
| chr21:38429715
|
A | G | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.237-6154T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429715 | ||||||
| chr21:38429721
|
CTA | C | 16 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(13): Show | 16 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.237-6162_237-6161d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429721 | ||||||
| chr21:38429735
|
GTA | G | 52 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(49): Show | 53 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.237-6176_237-6175d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429735 | ||||||
| chr21:38429736
|
T | C | 125 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(122): Show | 125 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.237-6175A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429736 | ||||||
| chr21:38429742
|
T | TACAC | 122 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(119): Show | 122 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.237-6182_237-6181i others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429742 | ||||||
| chr21:38429742
|
T | TACACAC | 3 | a0001c0001t0001g0072a0001c0001t0001g0104a0001c0001t0003g0280 | 3 | HG01346.hp2 HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.237-6182_237-6181i others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429742 | ||||||
| chr21:38429744
|
T | C | 126 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(123): Show | 126 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.237-6183A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429744 | ||||||
| chr21:38429744
|
T | TAC | 43 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.237-6184_237-6183i others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429744 | ||||||
| chr21:38429744
|
T | TACAC | 27 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(24): Show | 28 | HG00323.hp1 HG00438.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.237-6184_237-6183i others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429744 | ||||||
| chr21:38429744
|
T | TACACAC | 6 | a0001c0001t0001g0127a0001c0001t0001g0143a0001c0001t0001g0238others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-6184_237-6183i others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429744 | ||||||
| chr21:38429746
|
T | C | 294 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(291): Show | 296 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.237-6185A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429746 | ||||||
| chr21:38429817
|
T | G | 289 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(286): Show | 291 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.237-6256A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429817 | ||||||
| chr21:38429854
|
T | C | 56 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(53): Show | 57 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.237-6293A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429854 | ||||||
| chr21:38429932
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.237-6371T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429932 | ||||||
| chr21:38429977
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.237-6416C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38429977 | ||||||
| chr21:38430002
|
T | C | 1 | a0001c0001t0023g0339 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.237-6441A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430002 | ||||||
| chr21:38430081
|
AT | A | 115 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0066others(112): Show | 117 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.237-6521delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430081 | ||||||
| chr21:38430201
|
C | G | 117 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(114): Show | 117 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.237-6640G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430201 | ||||||
| chr21:38430644
|
C | T | 42 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.237-7083G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430644 | ||||||
| chr21:38430694
|
C | T | 3 | a0001c0001t0002g0265a0001c0001t0002g0349a0001c0001t0002g0350 | 3 | HG03041.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.237-7133G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430694 | ||||||
| chr21:38430744
|
A | G | 293 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(290): Show | 295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.237-7183T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430744 | ||||||
| chr21:38430814
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.237-7253T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430814 | ||||||
| chr21:38430870
|
C | G | 118 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(115): Show | 118 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.237-7309G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430870 | ||||||
| chr21:38430963
|
T | TA | 123 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(120): Show | 123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.237-7403dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38430963 | ||||||
| chr21:38431009
|
G | A | 1 | a0001c0001t0003g0188 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.237-7448C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431009 | ||||||
| chr21:38431104
|
T | C | 31 | a0001c0001t0001g0076a0001c0001t0001g0261a0001c0001t0001g0334others(28): Show | 31 | HG01346.hp1 HG01496.hp1 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.237-7543A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431104 | ||||||
| chr21:38431286
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.237-7725G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431286 | ||||||
| chr21:38431393
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.237-7832T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431393 | ||||||
| chr21:38431435
|
C | G | 1 | a0001c0001t0002g0304 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.237-7874G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431435 | ||||||
| chr21:38431435
|
C | T | 17 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(14): Show | 17 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-7874G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431435 | ||||||
| chr21:38431704
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.237-8143A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431704 | ||||||
| chr21:38431740
|
T | C | 100 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0076others(97): Show | 101 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.237-8179A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431740 | ||||||
| chr21:38431800
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.237-8239C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431800 | ||||||
| chr21:38431871
|
C | T | 68 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0086others(65): Show | 69 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.237-8310G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431871 | ||||||
| chr21:38431920
|
C | T | 5 | a0001c0001t0001g0234a0001c0001t0003g0302a0001c0001t0008g0171others(2): Show | 5 | HG02027.hp2 HG02257.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-8359G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431920 | ||||||
| chr21:38431941
|
T | C | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.237-8380A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38431941 | ||||||
| chr21:38432247
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0004g0023a0001c0001t0004g0033 | 3 | HG00733.hp2 HG01257.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.237-8686T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38432247 | ||||||
| chr21:38432361
|
T | C | 26 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0089others(23): Show | 26 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.237-8800A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38432361 | ||||||
| chr21:38432488
|
C | A | 301 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(298): Show | 303 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.237-8927G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38432488 | ||||||
| chr21:38432824
|
C | T | 7 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-9263G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38432824 | ||||||
| chr21:38432889
|
T | C | 1 | a0001c0001t0002g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.237-9328A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38432889 | ||||||
| chr21:38432918
|
A | G | 5 | a0001c0001t0001g0086a0001c0001t0001g0159a0001c0001t0001g0211others(2): Show | 5 | HG01081.hp2 HG01099.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-9357T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38432918 | ||||||
| chr21:38432943
|
C | T | 257 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(254): Show | 259 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.237-9382G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38432943 | ||||||
| chr21:38433065
|
A | C | 343 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(340): Show | 345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.237-9504T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433065 | ||||||
| chr21:38433173
|
G | C | 240 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(237): Show | 242 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.237-9612C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433173 | ||||||
| chr21:38433251
|
C | A | 1 | a0001c0001t0004g0007 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.237-9690G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433251 | ||||||
| chr21:38433256
|
G | A | 38 | a0001c0001t0001g0120a0001c0001t0001g0135a0001c0001t0001g0149others(35): Show | 38 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.237-9695C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433256 | ||||||
| chr21:38433336
|
A | G | 7 | a0001c0001t0001g0275a0001c0001t0001g0291a0001c0001t0002g0087others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-9775T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433336 | ||||||
| chr21:38433489
|
A | G | 3 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0347 | 3 | HG02145.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.237-9928T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433489 | ||||||
| chr21:38433581
|
G | A | 64 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0116others(61): Show | 65 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.237-10020C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433581 | ||||||
| chr21:38433654
|
G | T | 1 | a0001c0001t0002g0305 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.237-10093C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433654 | ||||||
| chr21:38433699
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.237-10138T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433699 | ||||||
| chr21:38433827
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.237-10266T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433827 | ||||||
| chr21:38433848
|
A | C | 1 | a0001c0001t0003g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.237-10287T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433848 | ||||||
| chr21:38433849
|
G | A | 1 | a0001c0001t0005g0003 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.237-10288C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433849 | ||||||
| chr21:38433875
|
G | A | 64 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0116others(61): Show | 65 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.237-10314C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433875 | ||||||
| chr21:38433953
|
A | G | 290 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(287): Show | 291 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.237-10392T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433953 | ||||||
| chr21:38433991
|
G | A | 173 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(170): Show | 174 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.237-10430C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38433991 | ||||||
| chr21:38434081
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.237-10520T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38434081 | ||||||
| chr21:38434205
|
A | G | 175 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(172): Show | 176 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.237-10644T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38434205 | ||||||
| chr21:38434259
|
C | T | 2 | a0001c0001t0003g0335a0001c0001t0003g0336 | 2 | HG02015.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.237-10698G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38434259 | ||||||
| chr21:38434325
|
T | A | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.237-10764A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38434325 | ||||||
| chr21:38434471
|
G | A | 52 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(49): Show | 53 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.237-10910C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38434471 | ||||||
| chr21:38434963
|
C | T | 317 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(314): Show | 319 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.236+10441G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38434963 | ||||||
| chr21:38435111
|
T | C | 32 | a0001c0001t0001g0076a0001c0001t0001g0261a0001c0001t0001g0334others(29): Show | 32 | HG01346.hp1 HG01496.hp1 HG01981.hp1 others(29): Show |
intron_variant | MODIFIER | c.236+10293A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435111 | ||||||
| chr21:38435114
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.236+10290C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435114 | ||||||
| chr21:38435140
|
C | A | 3 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343 | 3 | HG01167.hp1 HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.236+10264G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435140 | ||||||
| chr21:38435142
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.236+10262C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435142 | ||||||
| chr21:38435287
|
T | C | 1 | a0001c0001t0003g0062 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.236+10117A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435287 | ||||||
| chr21:38435343
|
C | G | 9 | a0001c0001t0001g0261a0001c0001t0002g0121a0001c0001t0002g0122others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.236+10061G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435343 | ||||||
| chr21:38435347
|
G | C | 17 | a0001c0001t0001g0158a0001c0001t0001g0202a0001c0001t0001g0255others(14): Show | 17 | HG00639.hp2 HG01106.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.236+10057C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435347 | ||||||
| chr21:38435388
|
C | G | 1 | a0001c0001t0003g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.236+10016G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435388 | ||||||
| chr21:38435409
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0234a0001c0001t0001g0239 | 3 | HG01167.hp2 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.236+9995G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435409 | ||||||
| chr21:38435431
|
G | A | 21 | a0001c0001t0001g0076a0001c0001t0001g0334a0001c0001t0002g0078others(18): Show | 21 | HG01346.hp1 HG01496.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.236+9973C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435431 | ||||||
| chr21:38435528
|
T | C | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.236+9876A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435528 | ||||||
| chr21:38435575
|
C | T | 329 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(326): Show | 331 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.236+9829G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435575 | ||||||
| chr21:38435590
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.236+9814T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435590 | ||||||
| chr21:38435595
|
T | C | 3 | a0001c0001t0007g0011a0001c0001t0007g0022a0001c0001t0030g0256 | 3 | HG01981.hp1 HG02148.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.236+9809A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435595 | ||||||
| chr21:38435727
|
G | A | 1 | a0001c0001t0023g0339 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.236+9677C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435727 | ||||||
| chr21:38435812
|
T | C | 1 | a0001c0006t0001g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.236+9592A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38435812 | ||||||
| chr21:38436019
|
T | C | 1 | a0001c0001t0001g0311 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.236+9385A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436019 | ||||||
| chr21:38436020
|
C | CT | 229 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(226): Show | 230 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(227): Show |
intron_variant | MODIFIER | c.236+9383dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436020 | ||||||
| chr21:38436020
|
C | CTT | 27 | a0001c0001t0001g0060a0001c0001t0001g0158a0001c0001t0001g0202others(24): Show | 27 | HG00639.hp2 HG01106.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.236+9382_236+9383d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436020 | ||||||
| chr21:38436167
|
A | AT | 137 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(134): Show | 137 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.236+9236dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436167 | ||||||
| chr21:38436276
|
A | G | 337 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(334): Show | 339 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.236+9128T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436276 | ||||||
| chr21:38436343
|
T | C | 64 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0120others(61): Show | 65 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.236+9061A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436343 | ||||||
| chr21:38436778
|
A | C | 320 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(317): Show | 322 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.236+8626T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436778 | ||||||
| chr21:38436779
|
T | C | 320 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(317): Show | 322 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.236+8625A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436779 | ||||||
| chr21:38436865
|
AG | A | 62 | a0001c0001t0001g0059a0001c0001t0001g0073a0001c0001t0001g0120others(59): Show | 63 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.236+8538delC | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436865 | ||||||
| chr21:38436880
|
CT | C | 317 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(314): Show | 319 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.236+8523delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436880 | ||||||
| chr21:38436899
|
C | CT | 220 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(217): Show | 221 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.236+8504dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436899 | ||||||
| chr21:38436899
|
C | CTT | 7 | a0001c0001t0002g0109a0001c0001t0002g0349a0001c0001t0002g0350others(4): Show | 7 | HG02080.hp2 HG03195.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.236+8503_236+8504d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436899 | ||||||
| chr21:38436991
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.236+8413C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38436991 | ||||||
| chr21:38437036
|
T | C | 142 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(139): Show | 142 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.236+8368A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437036 | ||||||
| chr21:38437186
|
G | A | 5 | a0001c0001t0002g0140a0001c0001t0002g0182a0001c0001t0002g0243others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.236+8218C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437186 | ||||||
| chr21:38437288
|
A | ACTTCGAC others(12): Show |
1 | a0001c0001t0001g0277 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.236+8097_236+8115d others(21): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437288 | ||||||
| chr21:38437355
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.236+8049G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437355 | ||||||
| chr21:38437438
|
C | T | 73 | a0001c0001t0001g0059a0001c0001t0001g0120a0001c0001t0001g0135others(70): Show | 73 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.236+7966G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437438 | ||||||
| chr21:38437469
|
T | C | 67 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(64): Show | 68 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.236+7935A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437469 | ||||||
| chr21:38437552
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.236+7852C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437552 | ||||||
| chr21:38437760
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.236+7644A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437760 | ||||||
| chr21:38437968
|
G | C | 14 | a0001c0001t0001g0202a0001c0001t0001g0275a0001c0001t0001g0291others(11): Show | 14 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.236+7436C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437968 | ||||||
| chr21:38437995
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.236+7409G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38437995 | ||||||
| chr21:38438052
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.236+7352G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438052 | ||||||
| chr21:38438067
|
T | G | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.236+7337A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438067 | ||||||
| chr21:38438154
|
A | C | 293 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(290): Show | 295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.236+7250T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438154 | ||||||
| chr21:38438160
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.236+7244G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438160 | ||||||
| chr21:38438261
|
C | T | 1 | a0001c0001t0002g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.236+7143G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438261 | ||||||
| chr21:38438275
|
T | C | 13 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0237others(10): Show | 13 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.236+7129A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438275 | ||||||
| chr21:38438288
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0145others(1): Show | 4 | HG02027.hp1 NA18963.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+7116A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438288 | ||||||
| chr21:38438328
|
T | C | 1 | a0001c0001t0002g0203 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.236+7076A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438328 | ||||||
| chr21:38438456
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.236+6948A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438456 | ||||||
| chr21:38438820
|
C | T | 65 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0135others(62): Show | 65 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.236+6584G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438820 | ||||||
| chr21:38438977
|
C | T | 1 | a0001c0001t0011g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.236+6427G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38438977 | ||||||
| chr21:38439071
|
A | G | 1 | a0001c0001t0002g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.236+6333T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439071 | ||||||
| chr21:38439080
|
A | C | 1 | a0001c0001t0001g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.236+6324T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439080 | ||||||
| chr21:38439086
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0001g0248a0001c0001t0004g0018 | 3 | NA18970.hp2 NA18973.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.236+6318C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439086 | ||||||
| chr21:38439150
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.236+6254G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439150 | ||||||
| chr21:38439239
|
G | A | 125 | a0001c0001t0001g0065a0001c0001t0001g0080a0001c0001t0001g0095others(122): Show | 125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.236+6165C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439239 | ||||||
| chr21:38439244
|
A | C | 6 | a0001c0001t0001g0261a0001c0001t0002g0123a0001c0001t0002g0124others(3): Show | 6 | HG02572.hp2 HG02622.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+6160T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439244 | ||||||
| chr21:38439694
|
G | T | 5 | a0001c0001t0001g0283a0001c0001t0002g0121a0001c0001t0002g0122others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+5710C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439694 | ||||||
| chr21:38439701
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.236+5703G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439701 | ||||||
| chr21:38439974
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.236+5430C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439974 | ||||||
| chr21:38439996
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0225 | 2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.236+5408G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38439996 | ||||||
| chr21:38440052
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.236+5352G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440052 | ||||||
| chr21:38440229
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.236+5175G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440229 | ||||||
| chr21:38440291
|
T | C | 1 | a0001c0001t0004g0024 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.236+5113A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440291 | ||||||
| chr21:38440326
|
G | T | 54 | a0001c0001t0001g0059a0001c0001t0001g0089a0001c0001t0001g0107others(51): Show | 54 | HG00438.hp2 HG00609.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.236+5078C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440326 | ||||||
| chr21:38440437
|
A | T | 1 | a0001c0001t0001g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.236+4967T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440437 | ||||||
| chr21:38440466
|
T | C | 14 | a0001c0001t0001g0173a0001c0001t0001g0200a0001c0001t0001g0206others(11): Show | 14 | HG00738.hp1 HG01099.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.236+4938A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440466 | ||||||
| chr21:38440517
|
A | G | 2 | a0001c0001t0002g0352a0002c0004t0003g0356 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.236+4887T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440517 | ||||||
| chr21:38440558
|
C | T | 108 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0073others(105): Show | 108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.236+4846G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440558 | ||||||
| chr21:38440655
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.236+4749G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440655 | ||||||
| chr21:38440681
|
C | T | 3 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301 | 3 | NA18988.hp2 NA19056.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.236+4723G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440681 | ||||||
| chr21:38440750
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0031g0358 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.236+4654A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440750 | ||||||
| chr21:38440778
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.236+4626T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440778 | ||||||
| chr21:38440787
|
CAAA | C | 20 | a0001c0001t0001g0098a0001c0001t0001g0105a0001c0001t0001g0116others(17): Show | 20 | HG01243.hp2 HG01257.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.236+4614_236+4616d others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440787 | ||||||
| chr21:38440787
|
CAAAA | C | 140 | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0001g0066others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.236+4613_236+4616d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440787 | ||||||
| chr21:38440787
|
CAAAAAAA | C | 43 | a0001c0001t0001g0059a0001c0001t0001g0079a0001c0001t0001g0082others(40): Show | 43 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.236+4610_236+4616d others(9): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440787 | ||||||
| chr21:38440787
|
CAAAAAAA others(2): Show |
C | 75 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0120others(72): Show | 75 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.236+4608_236+4616d others(11): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440787 | ||||||
| chr21:38440787
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0135a0001c0001t0003g0257 | 2 | HG04115.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.236+4607_236+4616d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440787 | ||||||
| chr21:38440787
|
CAAAAAAA others(4): Show |
C | 29 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0200others(26): Show | 29 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.236+4606_236+4616d others(13): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38440787 | ||||||
| chr21:38441049
|
C | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0354 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.236+4355G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441049 | ||||||
| chr21:38441162
|
A | G | 27 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0143others(24): Show | 27 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.236+4242T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441162 | ||||||
| chr21:38441248
|
GC | G | 10 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0330others(7): Show | 10 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.236+4155delG | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441248 | ||||||
| chr21:38441348
|
TA | T | 10 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0330others(7): Show | 10 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.236+4055delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441348 | ||||||
| chr21:38441364
|
T | C | 165 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.236+4040A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441364 | ||||||
| chr21:38441595
|
C | G | 165 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(162): Show | 165 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.236+3809G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441595 | ||||||
| chr21:38441734
|
G | T | 166 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(163): Show | 166 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.236+3670C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441734 | ||||||
| chr21:38441743
|
C | G | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.236+3661G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441743 | ||||||
| chr21:38441768
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.236+3636G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441768 | ||||||
| chr21:38441843
|
G | A | 11 | a0001c0001t0001g0173a0001c0001t0001g0200a0001c0001t0001g0206others(8): Show | 11 | HG00738.hp1 HG01099.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+3561C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441843 | ||||||
| chr21:38441985
|
A | C | 28 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0143others(25): Show | 28 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.236+3419T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38441985 | ||||||
| chr21:38442029
|
T | A | 17 | a0001c0001t0001g0173a0001c0001t0001g0200a0001c0001t0001g0206others(14): Show | 17 | HG00738.hp1 HG01099.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.236+3375A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442029 | ||||||
| chr21:38442032
|
T | C | 208 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.236+3372A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442032 | ||||||
| chr21:38442089
|
A | G | 1 | a0002c0004t0003g0356 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236+3315T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442089 | ||||||
| chr21:38442132
|
G | A | 23 | a0001c0001t0001g0059a0001c0001t0001g0127a0001c0001t0001g0189others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.236+3272C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442132 | ||||||
| chr21:38442252
|
G | A | 10 | a0001c0001t0001g0059a0001c0001t0001g0189a0001c0001t0001g0209others(7): Show | 10 | HG00323.hp1 HG00438.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.236+3152C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442252 | ||||||
| chr21:38442319
|
C | CG | 14 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0259others(11): Show | 14 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.236+3084dupC | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442319 | ||||||
| chr21:38442322
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.236+3082C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442322 | ||||||
| chr21:38442328
|
G | C | 18 | a0001c0001t0001g0059a0001c0001t0001g0127a0001c0001t0001g0189others(15): Show | 18 | HG00323.hp1 HG00438.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.236+3076C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442328 | ||||||
| chr21:38442349
|
C | T | 6 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0153others(3): Show | 6 | NA18959.hp1 NA18967.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+3055G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442349 | ||||||
| chr21:38442446
|
T | C | 10 | a0001c0001t0001g0086a0001c0001t0001g0282a0001c0001t0002g0141others(7): Show | 10 | HG01099.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.236+2958A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442446 | ||||||
| chr21:38442447
|
T | G | 1 | a0001c0001t0003g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.236+2957A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442447 | ||||||
| chr21:38442451
|
C | T | 23 | a0001c0001t0001g0059a0001c0001t0001g0127a0001c0001t0001g0189others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.236+2953G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442451 | ||||||
| chr21:38442475
|
C | A | 4 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0203others(1): Show | 4 | HG02280.hp1 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+2929G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442475 | ||||||
| chr21:38442573
|
T | C | 10 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0330others(7): Show | 10 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.236+2831A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442573 | ||||||
| chr21:38442582
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.236+2822C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442582 | ||||||
| chr21:38442588
|
G | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0206a0001c0001t0001g0220 | 3 | NA18943.hp2 NA18962.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.236+2816C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442588 | ||||||
| chr21:38442852
|
G | A | 1 | a0001c0001t0003g0270 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.236+2552C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442852 | ||||||
| chr21:38442868
|
C | T | 3 | a0001c0001t0001g0259a0001c0001t0002g0254a0001c0001t0011g0279 | 3 | HG02559.hp2 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.236+2536G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38442868 | ||||||
| chr21:38443103
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.236+2301C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443103 | ||||||
| chr21:38443289
|
T | C | 168 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.236+2115A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443289 | ||||||
| chr21:38443322
|
T | A | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0203 | 3 | HG03195.hp2 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.236+2082A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443322 | ||||||
| chr21:38443344
|
C | T | 301 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.236+2060G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443344 | ||||||
| chr21:38443404
|
A | G | 2 | a0001c0001t0001g0259a0001c0001t0011g0279 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.236+2000T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443404 | ||||||
| chr21:38443445
|
C | T | 24 | a0001c0001t0001g0059a0001c0001t0001g0127a0001c0001t0001g0189others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.236+1959G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443445 | ||||||
| chr21:38443597
|
A | C | 22 | a0001c0001t0001g0059a0001c0001t0001g0127a0001c0001t0001g0187others(19): Show | 22 | HG00323.hp1 HG00438.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.236+1807T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443597 | ||||||
| chr21:38443601
|
A | C | 37 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0117others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.236+1803T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443601 | ||||||
| chr21:38443607
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.236+1797T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443607 | ||||||
| chr21:38443653
|
T | C | 160 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.236+1751A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443653 | ||||||
| chr21:38443916
|
A | C | 169 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.236+1488T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443916 | ||||||
| chr21:38443928
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0008g0297a0001c0001t0014g0075others(1): Show | 4 | HG01978.hp1 HG02027.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+1476G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443928 | ||||||
| chr21:38443983
|
C | T | 8 | a0001c0001t0001g0143a0001c0001t0001g0258a0001c0001t0001g0264others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+1421G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443983 | ||||||
| chr21:38443989
|
C | G | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.236+1415G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443989 | ||||||
| chr21:38443990
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.236+1414A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38443990 | ||||||
| chr21:38444037
|
C | A | 40 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0117others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.236+1367G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444037 | ||||||
| chr21:38444058
|
T | C | 2 | a0001c0001t0002g0349a0001c0001t0002g0350 | 2 | NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.236+1346A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444058 | ||||||
| chr21:38444107
|
A | G | 1 | a0001c0001t0002g0349 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236+1297T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444107 | ||||||
| chr21:38444265
|
C | T | 31 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0076others(28): Show | 31 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.236+1139G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444265 | ||||||
| chr21:38444296
|
G | A | 4 | a0001c0001t0001g0283a0001c0001t0002g0121a0001c0001t0002g0122others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+1108C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444296 | ||||||
| chr21:38444405
|
G | T | 169 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(166): Show | 169 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.236+999C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444405 | ||||||
| chr21:38444556
|
A | G | 1 | a0001c0001t0021g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.236+848T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444556 | ||||||
| chr21:38444694
|
T | C | 351 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(348): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.236+710A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444694 | ||||||
| chr21:38444726
|
G | GA | 186 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.236+677dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444726 | ||||||
| chr21:38444726
|
G | GAA | 8 | a0001c0001t0001g0086a0001c0001t0001g0105a0001c0001t0003g0057others(5): Show | 8 | HG01099.hp1 HG01167.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+676_236+677dup others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444726 | ||||||
| chr21:38444739
|
AAC | A | 16 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0158others(13): Show | 16 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.236+663_236+664del others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444739 | ||||||
| chr21:38444740
|
AC | A | 20 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0143others(17): Show | 20 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.236+663delG | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444740 | ||||||
| chr21:38444788
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.236+616C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444788 | ||||||
| chr21:38444848
|
G | A | 166 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(163): Show | 166 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.236+556C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444848 | ||||||
| chr21:38444899
|
C | T | 37 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0117others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.236+505G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38444899 | ||||||
| chr21:38445090
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.236+314C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445090 | ||||||
| chr21:38445099
|
C | T | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.236+305G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445099 | ||||||
| chr21:38445100
|
G | A | 11 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0330others(8): Show | 11 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.236+304C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445100 | ||||||
| chr21:38445105
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.236+299G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445105 | ||||||
| chr21:38445138
|
C | CT | 12 | a0001c0001t0001g0058a0001c0001t0001g0101a0001c0001t0001g0106others(9): Show | 12 | HG00099.hp2 HG02132.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+265dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445138 | ||||||
| chr21:38445138
|
CT | C | 29 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0143others(26): Show | 29 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.236+265delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445138 | ||||||
| chr21:38445140
|
T | TC | 8 | a0001c0001t0001g0070a0001c0001t0001g0128a0001c0001t0001g0153others(5): Show | 8 | HG01952.hp2 HG02148.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+263_236+264ins others(1): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445140 | ||||||
| chr21:38445141
|
T | C | 68 | a0001c0001t0001g0059a0001c0001t0001g0072a0001c0001t0001g0076others(65): Show | 68 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.236+263A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445141 | ||||||
| chr21:38445144
|
T | C | 4 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(1): Show | 4 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+260A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445144 | ||||||
| chr21:38445163
|
C | A | 1 | a0001c0002t0012g0228 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.236+241G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445163 | ||||||
| chr21:38445267
|
G | A | 2 | a0001c0001t0002g0349a0001c0001t0002g0350 | 2 | NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.236+137C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445267 | ||||||
| chr21:38445369
|
A | G | 1 | a0001c0001t0009g0154 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.236+35T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 2/9 | chr21 | 38445369 | ||||||
| chr21:38445811
|
C | T | 1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.19-190G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38445811 | ||||||
| chr21:38445814
|
C | T | 1 | a0001c0003t0001g0293 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.19-193G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38445814 | ||||||
| chr21:38446011
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.19-390T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446011 | ||||||
| chr21:38446023
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.19-402C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446023 | ||||||
| chr21:38446090
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0004g0052 | 2 | HG01433.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.19-469C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446090 | ||||||
| chr21:38446226
|
CA | C | 68 | a0001c0001t0001g0072a0001c0001t0001g0079a0001c0001t0001g0082others(65): Show | 70 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.19-606delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446226 | ||||||
| chr21:38446226
|
CAA | C | 87 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0076others(84): Show | 87 | HG00639.hp2 HG00673.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.19-607_19-606delTT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446226 | ||||||
| chr21:38446226
|
CAAA | C | 174 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.19-608_19-606delTT others(1): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446226 | ||||||
| chr21:38446226
|
CAAAAAAA others(9): Show |
C | 9 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0191others(6): Show | 9 | HG00323.hp2 HG01169.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-621_19-606delTT others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446226 | ||||||
| chr21:38446323
|
T | C | 166 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.19-702A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446323 | ||||||
| chr21:38446389
|
G | A | 1 | a0001c0001t0014g0075 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.19-768C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446389 | ||||||
| chr21:38446412
|
T | A | 2 | a0001c0001t0001g0202a0001c0001t0002g0265 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.19-791A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446412 | ||||||
| chr21:38446452
|
G | A | 4 | a0001c0001t0001g0283a0001c0001t0002g0121a0001c0001t0002g0122others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-831C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446452 | ||||||
| chr21:38446550
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0004g0026 | 2 | HG02132.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.19-929T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446550 | ||||||
| chr21:38446748
|
G | A | 1 | a0001c0001t0006g0053 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.19-1127C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446748 | ||||||
| chr21:38446778
|
C | T | 15 | a0001c0001t0001g0173a0001c0001t0001g0200a0001c0001t0001g0206others(12): Show | 15 | HG00738.hp1 HG01099.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-1157G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446778 | ||||||
| chr21:38446845
|
A | T | 2 | a0001c0001t0001g0344a0001c0001t0026g0125 | 2 | HG01106.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.19-1224T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446845 | ||||||
| chr21:38446915
|
C | A | 29 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0076others(26): Show | 29 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-1294G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38446915 | ||||||
| chr21:38447000
|
G | C | 165 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-1379C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38447000 | ||||||
| chr21:38447152
|
GT | G | 30 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0120others(27): Show | 30 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.19-1532delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38447152 | ||||||
| chr21:38447409
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.19-1788G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38447409 | ||||||
| chr21:38447640
|
A | G | 33 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0076others(30): Show | 33 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.19-2019T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38447640 | ||||||
| chr21:38447819
|
G | A | 6 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0002g0126others(3): Show | 6 | HG00099.hp1 HG02723.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-2198C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38447819 | ||||||
| chr21:38447907
|
C | T | 102 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0072others(99): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.19-2286G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38447907 | ||||||
| chr21:38447993
|
A | G | 1 | a0001c0001t0023g0339 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.19-2372T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38447993 | ||||||
| chr21:38448001
|
A | G | 8 | a0001c0001t0001g0127a0001c0001t0001g0238a0001c0001t0001g0259others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-2380T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38448001 | ||||||
| chr21:38448005
|
TA | T | 81 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0072others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.19-2385delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38448005 | ||||||
| chr21:38448088
|
TA | T | 8 | a0001c0001t0001g0127a0001c0001t0001g0238a0001c0001t0001g0259others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-2468delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38448088 | ||||||
| chr21:38448485
|
T | C | 190 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(187): Show | 190 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.19-2864A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38448485 | ||||||
| chr21:38448852
|
T | C | 6 | a0001c0001t0001g0238a0001c0001t0001g0261a0001c0001t0001g0281others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-3231A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38448852 | ||||||
| chr21:38448951
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.19-3330A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38448951 | ||||||
| chr21:38449062
|
G | C | 4 | a0001c0001t0001g0258a0001c0001t0001g0264a0001c0001t0003g0321others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-3441C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449062 | ||||||
| chr21:38449085
|
G | A | 1 | a0001c0001t0011g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19-3464C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449085 | ||||||
| chr21:38449250
|
T | C | 23 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0077others(20): Show | 23 | HG00642.hp2 HG00738.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.19-3629A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449250 | ||||||
| chr21:38449342
|
A | G | 32 | a0001c0001t0001g0061a0001c0001t0001g0080a0001c0001t0001g0135others(29): Show | 32 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.19-3721T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449342 | ||||||
| chr21:38449428
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.19-3807C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449428 | ||||||
| chr21:38449436
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.19-3815G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449436 | ||||||
| chr21:38449462
|
T | C | 1 | a0001c0001t0001g0353 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.19-3841A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449462 | ||||||
| chr21:38449476
|
G | A | 6 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0140others(3): Show | 6 | HG02622.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-3855C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449476 | ||||||
| chr21:38449543
|
T | A | 1 | a0001c0001t0006g0006 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.19-3922A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449543 | ||||||
| chr21:38449820
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.19-4199A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449820 | ||||||
| chr21:38449862
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-4241A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38449862 | ||||||
| chr21:38450091
|
T | TA | 15 | a0001c0001t0001g0108a0001c0001t0001g0135a0001c0001t0001g0211others(12): Show | 15 | HG00639.hp2 HG01884.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-4471dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450091 | ||||||
| chr21:38450091
|
TA | T | 11 | a0001c0001t0001g0136a0001c0001t0001g0238a0001c0001t0001g0239others(8): Show | 12 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.19-4471delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450091 | ||||||
| chr21:38450114
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0002g0265 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.19-4493C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450114 | ||||||
| chr21:38450220
|
GA | G | 321 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(318): Show | 321 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.19-4600delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450220 | ||||||
| chr21:38450239
|
G | A | 13 | a0001c0001t0001g0059a0001c0001t0001g0107a0001c0001t0001g0209others(10): Show | 13 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.19-4618C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450239 | ||||||
| chr21:38450321
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.19-4700A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450321 | ||||||
| chr21:38450336
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.19-4715G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450336 | ||||||
| chr21:38450380
|
AAAAAT | A | 8 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0140others(5): Show | 8 | HG02622.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-4764_19-4760del others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450380 | ||||||
| chr21:38450523
|
C | T | 8 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0002g0126others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-4902G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450523 | ||||||
| chr21:38450663
|
C | T | 3 | a0001c0001t0002g0235a0001c0001t0003g0208a0001c0001t0010g0084 | 3 | HG00639.hp1 HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.19-5042G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450663 | ||||||
| chr21:38450679
|
G | A | 2 | a0001c0001t0030g0256a0001c0001t0031g0358 | 2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-5058C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450679 | ||||||
| chr21:38450727
|
G | T | 322 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(319): Show | 322 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.19-5106C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450727 | ||||||
| chr21:38450739
|
C | G | 4 | a0001c0001t0001g0186a0001c0001t0001g0287a0001c0001t0001g0344others(1): Show | 4 | HG02451.hp2 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-5118G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450739 | ||||||
| chr21:38450740
|
A | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0155 | 2 | NA19065.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.19-5119T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450740 | ||||||
| chr21:38450803
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.19-5182A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450803 | ||||||
| chr21:38450983
|
G | C | 325 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(322): Show | 325 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(322): Show |
intron_variant | MODIFIER | c.19-5362C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38450983 | ||||||
| chr21:38451063
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.19-5442A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451063 | ||||||
| chr21:38451142
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.19-5521C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451142 | ||||||
| chr21:38451318
|
C | G | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.19-5697G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451318 | ||||||
| chr21:38451426
|
T | C | 271 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(268): Show | 271 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.19-5805A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451426 | ||||||
| chr21:38451509
|
G | A | 5 | a0001c0001t0003g0188a0001c0001t0003g0222a0001c0001t0003g0223others(2): Show | 5 | HG00642.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-5888C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451509 | ||||||
| chr21:38451528
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.19-5907G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451528 | ||||||
| chr21:38451762
|
C | T | 5 | a0001c0001t0001g0143a0001c0001t0001g0202a0001c0001t0002g0134others(2): Show | 5 | HG00735.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-6141G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451762 | ||||||
| chr21:38451783
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0003g0337 | 2 | NA18987.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.19-6162T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451783 | ||||||
| chr21:38451791
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.19-6170T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38451791 | ||||||
| chr21:38452003
|
C | A | 1 | a0001c0001t0002g0249 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.19-6382G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452003 | ||||||
| chr21:38452067
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.19-6446A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452067 | ||||||
| chr21:38452130
|
AAG | A | 31 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0072others(28): Show | 31 | HG00558.hp1 HG00609.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.19-6511_19-6510del others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452130 | ||||||
| chr21:38452244
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0291a0001c0001t0004g0024 | 3 | HG00323.hp2 HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.19-6623G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452244 | ||||||
| chr21:38452250
|
G | T | 315 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(312): Show | 315 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.19-6629C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452250 | ||||||
| chr21:38452322
|
C | T | 124 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0065others(121): Show | 124 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.19-6701G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452322 | ||||||
| chr21:38452323
|
G | A | 1 | a0001c0001t0005g0032 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.19-6702C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452323 | ||||||
| chr21:38452340
|
T | C | 16 | a0001c0001t0001g0059a0001c0001t0001g0107a0001c0001t0001g0187others(13): Show | 16 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.19-6719A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452340 | ||||||
| chr21:38452340
|
TAC | T | 5 | a0001c0001t0001g0096a0001c0001t0003g0069a0001c0001t0003g0229others(2): Show | 5 | HG00280.hp1 HG00280.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-6721_19-6720del others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452340 | ||||||
| chr21:38452362
|
C | T | 7 | a0001c0001t0001g0136a0001c0001t0001g0316a0001c0001t0002g0299others(4): Show | 8 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-6741G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452362 | ||||||
| chr21:38452474
|
A | G | 298 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(295): Show | 298 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.19-6853T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452474 | ||||||
| chr21:38452751
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.19-7130G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452751 | ||||||
| chr21:38452834
|
G | C | 2 | a0001c0001t0030g0256a0001c0001t0031g0358 | 2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-7213C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452834 | ||||||
| chr21:38452874
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.19-7253A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38452874 | ||||||
| chr21:38453054
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.19-7433G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453054 | ||||||
| chr21:38453089
|
C | T | 270 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(267): Show | 270 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.19-7468G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453089 | ||||||
| chr21:38453274
|
A | G | 8 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0002g0126others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-7653T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453274 | ||||||
| chr21:38453366
|
T | G | 1 | a0001c0001t0003g0321 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.19-7745A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453366 | ||||||
| chr21:38453474
|
C | T | 14 | a0001c0001t0001g0211a0001c0001t0001g0275a0001c0001t0001g0323others(11): Show | 14 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-7853G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453474 | ||||||
| chr21:38453648
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.19-8027G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453648 | ||||||
| chr21:38453660
|
A | G | 2 | a0001c0001t0002g0087a0001c0001t0003g0270 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.19-8039T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453660 | ||||||
| chr21:38453811
|
G | A | 1 | a0001c0001t0024g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.19-8190C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453811 | ||||||
| chr21:38453815
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19-8194C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453815 | ||||||
| chr21:38453845
|
C | T | 318 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(315): Show | 318 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.19-8224G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453845 | ||||||
| chr21:38453858
|
T | C | 1 | a0001c0001t0001g0327 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.19-8237A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453858 | ||||||
| chr21:38453882
|
C | CA | 23 | a0001c0001t0001g0061a0001c0001t0001g0202a0001c0001t0001g0259others(20): Show | 23 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.19-8262dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453882 | ||||||
| chr21:38453882
|
C | CAA | 121 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0070others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.19-8263_19-8262dup others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453882 | ||||||
| chr21:38453882
|
C | CAAA | 137 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(134): Show | 137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.19-8264_19-8262dup others(3): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453882 | ||||||
| chr21:38453882
|
C | CAAAA | 6 | a0001c0001t0001g0176a0001c0001t0001g0227a0001c0001t0002g0168others(3): Show | 6 | HG01978.hp2 HG02074.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-8265_19-8262dup others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38453882 | ||||||
| chr21:38454110
|
T | C | 319 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(316): Show | 319 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.19-8489A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454110 | ||||||
| chr21:38454133
|
T | A | 269 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(266): Show | 269 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.19-8512A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454133 | ||||||
| chr21:38454222
|
T | C | 269 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(266): Show | 269 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.19-8601A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454222 | ||||||
| chr21:38454262
|
G | A | 316 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(313): Show | 316 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.19-8641C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454262 | ||||||
| chr21:38454275
|
C | T | 8 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0002g0126others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-8654G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454275 | ||||||
| chr21:38454426
|
C | T | 2 | a0001c0001t0001g0323a0001c0001t0002g0246 | 2 | HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.19-8805G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454426 | ||||||
| chr21:38454511
|
CT | C | 12 | a0001c0001t0001g0107a0001c0001t0001g0209a0001c0001t0001g0239others(9): Show | 12 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.19-8891delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454511 | ||||||
| chr21:38454693
|
C | T | 1 | a0001c0001t0008g0171 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.19-9072G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454693 | ||||||
| chr21:38454852
|
C | T | 33 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0120others(30): Show | 33 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.19-9231G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454852 | ||||||
| chr21:38454899
|
C | T | 5 | a0001c0001t0001g0143a0001c0001t0001g0202a0001c0001t0002g0134others(2): Show | 5 | HG00735.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-9278G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38454899 | ||||||
| chr21:38455020
|
C | T | 10 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0002g0123others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.19-9399G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455020 | ||||||
| chr21:38455094
|
T | TTTTC | 7 | a0001c0001t0001g0167a0001c0001t0001g0215a0001c0001t0001g0216others(4): Show | 7 | HG00597.hp2 HG02165.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-9477_19-9474dup others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455094 | ||||||
| chr21:38455094
|
TTTTC | T | 9 | a0001c0001t0001g0211a0001c0001t0001g0275a0001c0001t0002g0185others(6): Show | 9 | HG01167.hp1 HG01975.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-9477_19-9474del others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455094 | ||||||
| chr21:38455110
|
CTTTCTTT others(3): Show |
C | 2 | a0001c0001t0002g0296a0001c0001t0005g0005 | 2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.19-9499_19-9490del others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455110 | ||||||
| chr21:38455114
|
CTTTCT | C | 8 | a0001c0001t0001g0238a0001c0001t0001g0261a0001c0001t0001g0281others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-9498_19-9494del others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455114 | ||||||
| chr21:38455114
|
CTTTCTT | C | 112 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0066others(109): Show | 112 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.19-9499_19-9494del others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455114 | ||||||
| chr21:38455118
|
CT | C | 23 | a0001c0001t0001g0096a0001c0001t0001g0120a0001c0001t0001g0191others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.19-9498delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455118 | ||||||
| chr21:38455118
|
CTT | C | 145 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0064others(142): Show | 145 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.19-9499_19-9498del others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455118 | ||||||
| chr21:38455118
|
CTTT | C | 10 | a0001c0001t0001g0105a0001c0001t0002g0123a0001c0001t0002g0124others(7): Show | 10 | HG01346.hp2 HG02622.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-9500_19-9498del others(3): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455118 | ||||||
| chr21:38455118
|
CTTTTT | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0231a0001c0001t0001g0236others(6): Show | 9 | HG01433.hp1 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-9502_19-9498del others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455118 | ||||||
| chr21:38455119
|
T | TTTC | 6 | a0001c0001t0001g0234a0001c0001t0001g0291a0001c0001t0001g0292others(3): Show | 6 | HG00323.hp2 HG01358.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-9499_19-9498ins others(3): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455119 | ||||||
| chr21:38455123
|
T | C | 25 | a0001c0001t0001g0096a0001c0001t0001g0120a0001c0001t0001g0191others(22): Show | 25 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.19-9502A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455123 | ||||||
| chr21:38455127
|
T | C | 1 | a0001c0001t0003g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19-9506A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455127 | ||||||
| chr21:38455303
|
G | A | 20 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0001g0283others(17): Show | 20 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.19-9682C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455303 | ||||||
| chr21:38455348
|
C | T | 1 | a0001c0001t0016g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.19-9727G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455348 | ||||||
| chr21:38455404
|
G | A | 8 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0140others(5): Show | 8 | HG02622.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-9783C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455404 | ||||||
| chr21:38455502
|
C | A | 33 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0120others(30): Show | 33 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.19-9881G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455502 | ||||||
| chr21:38455516
|
G | A | 6 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0002g0126others(3): Show | 6 | HG02055.hp1 HG02723.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-9895C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455516 | ||||||
| chr21:38455627
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-10006G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455627 | ||||||
| chr21:38455810
|
C | T | 34 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0120others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.19-10189G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455810 | ||||||
| chr21:38455871
|
C | T | 2 | a0001c0001t0002g0295a0001c0001t0005g0050 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.19-10250G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455871 | ||||||
| chr21:38455877
|
T | C | 34 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0120others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.19-10256A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455877 | ||||||
| chr21:38455994
|
C | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0275a0001c0001t0003g0113others(1): Show | 4 | HG01975.hp1 HG02155.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-10373G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38455994 | ||||||
| chr21:38456072
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.19-10451A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456072 | ||||||
| chr21:38456144
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.19-10523A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456144 | ||||||
| chr21:38456386
|
G | A | 6 | a0001c0001t0001g0238a0001c0001t0001g0261a0001c0001t0001g0281others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-10765C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456386 | ||||||
| chr21:38456395
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.19-10774C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456395 | ||||||
| chr21:38456548
|
T | C | 1 | a0001c0001t0011g0279 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.19-10927A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456548 | ||||||
| chr21:38456598
|
C | CAG | 325 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(322): Show | 325 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(322): Show |
intron_variant | MODIFIER | c.19-10978_19-10977i others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456598 | ||||||
| chr21:38456726
|
G | C | 1 | a0001c0001t0004g0052 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.19-11105C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456726 | ||||||
| chr21:38456826
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.19-11205A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456826 | ||||||
| chr21:38456921
|
A | G | 322 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(319): Show | 322 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.19-11300T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456921 | ||||||
| chr21:38456986
|
T | C | 1 | a0001c0001t0011g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19-11365A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38456986 | ||||||
| chr21:38457211
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.19-11590G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457211 | ||||||
| chr21:38457324
|
T | C | 34 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0120others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.19-11703A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457324 | ||||||
| chr21:38457346
|
G | A | 8 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0002g0126others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-11725C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457346 | ||||||
| chr21:38457435
|
CA | C | 285 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(282): Show | 285 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.19-11815delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457435 | ||||||
| chr21:38457435
|
CAA | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0120others(29): Show | 32 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.19-11816_19-11815d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457435 | ||||||
| chr21:38457480
|
A | C | 1 | a0001c0001t0003g0298 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.19-11859T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457480 | ||||||
| chr21:38457726
|
G | A | 8 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0140others(5): Show | 8 | HG02622.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-12105C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457726 | ||||||
| chr21:38457778
|
G | A | 1 | a0001c0001t0010g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.19-12157C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457778 | ||||||
| chr21:38457826
|
C | G | 6 | a0001c0001t0001g0167a0001c0001t0001g0216a0001c0001t0001g0217others(3): Show | 6 | HG00597.hp2 HG02523.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-12205G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457826 | ||||||
| chr21:38457899
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0152 | 3 | NA18963.hp2 NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.19-12278C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38457899 | ||||||
| chr21:38458057
|
C | T | 1 | a0001c0001t0001g0340 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.19-12436G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458057 | ||||||
| chr21:38458073
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.19-12452G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458073 | ||||||
| chr21:38458118
|
C | G | 1 | a0001c0001t0002g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.19-12497G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458118 | ||||||
| chr21:38458137
|
G | A | 50 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0120others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.19-12516C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458137 | ||||||
| chr21:38458187
|
A | G | 1 | a0001c0001t0004g0007 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.19-12566T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458187 | ||||||
| chr21:38458222
|
G | A | 2 | a0001c0001t0002g0295a0001c0001t0005g0050 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.19-12601C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458222 | ||||||
| chr21:38458319
|
T | G | 17 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0001g0271others(14): Show | 17 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-12698A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458319 | ||||||
| chr21:38458384
|
A | G | 6 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0140others(3): Show | 6 | HG02622.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-12763T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458384 | ||||||
| chr21:38458423
|
C | CA | 113 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0065others(110): Show | 113 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.19-12803dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458423 | ||||||
| chr21:38458423
|
C | CAA | 16 | a0001c0001t0001g0129a0001c0001t0001g0200a0001c0001t0001g0206others(13): Show | 16 | HG00639.hp2 HG00738.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.19-12804_19-12803d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458423 | ||||||
| chr21:38458423
|
CAA | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0120others(29): Show | 32 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.19-12804_19-12803d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458423 | ||||||
| chr21:38458523
|
C | T | 1 | a0001c0001t0031g0358 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.19-12902G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458523 | ||||||
| chr21:38458627
|
C | T | 7 | a0001c0001t0001g0120a0001c0001t0001g0191a0001c0001t0001g0234others(4): Show | 7 | HG00323.hp2 HG01169.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-13006G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458627 | ||||||
| chr21:38458633
|
C | T | 44 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0117others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.19-13012G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458633 | ||||||
| chr21:38458697
|
C | T | 42 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0117others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.19-13076G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458697 | ||||||
| chr21:38458713
|
T | G | 1 | a0001c0001t0001g0354 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.19-13092A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38458713 | ||||||
| chr21:38459034
|
C | A | 1 | a0001c0001t0002g0341 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.19-13413G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459034 | ||||||
| chr21:38459122
|
A | C | 2 | a0001c0001t0002g0170a0001c0001t0002g0225 | 2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.19-13501T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459122 | ||||||
| chr21:38459268
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.19-13647T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459268 | ||||||
| chr21:38459328
|
T | C | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0203 | 3 | HG03195.hp2 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19-13707A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459328 | ||||||
| chr21:38459391
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.19-13770C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459391 | ||||||
| chr21:38459471
|
C | T | 5 | a0001c0001t0003g0241a0001c0001t0003g0342a0001c0001t0003g0343others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-13850G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459471 | ||||||
| chr21:38459473
|
A | G | 4 | a0001c0001t0002g0322a0001c0001t0002g0352a0001c0001t0011g0232others(1): Show | 4 | HG02451.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-13852T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459473 | ||||||
| chr21:38459737
|
G | C | 247 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.19-14116C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459737 | ||||||
| chr21:38459873
|
C | T | 77 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0104others(74): Show | 78 | HG00558.hp1 HG00733.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.19-14252G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459873 | ||||||
| chr21:38459902
|
C | T | 10 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0001g0167others(7): Show | 10 | HG00609.hp2 HG02027.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.19-14281G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38459902 | ||||||
| chr21:38460096
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.19-14475G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460096 | ||||||
| chr21:38460163
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.19-14542C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460163 | ||||||
| chr21:38460295
|
A | G | 4 | a0001c0001t0001g0281a0001c0001t0002g0141a0001c0001t0002g0142others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-14674T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460295 | ||||||
| chr21:38460414
|
A | C | 1 | a0001c0001t0003g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.19-14793T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460414 | ||||||
| chr21:38460417
|
T | A | 1 | a0001c0001t0003g0302 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19-14796A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460417 | ||||||
| chr21:38460418
|
C | T | 1 | a0001c0001t0003g0302 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19-14797G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460418 | ||||||
| chr21:38460419
|
T | C | 1 | a0001c0001t0003g0302 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19-14798A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460419 | ||||||
| chr21:38460429
|
T | C | 1 | a0001c0001t0019g0047 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.19-14808A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460429 | ||||||
| chr21:38460795
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.19-15174C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460795 | ||||||
| chr21:38460837
|
G | A | 4 | a0001c0001t0001g0101a0001c0001t0003g0335a0001c0001t0003g0336others(1): Show | 4 | HG02015.hp1 HG02056.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-15216C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38460837 | ||||||
| chr21:38461106
|
A | T | 1 | a0001c0001t0006g0038 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.19-15485T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461106 | ||||||
| chr21:38461137
|
T | C | 53 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0115others(50): Show | 53 | HG00544.hp2 HG00609.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.19-15516A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461137 | ||||||
| chr21:38461150
|
G | A | 2 | a0001c0001t0006g0036a0001c0001t0015g0037 | 2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.19-15529C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461150 | ||||||
| chr21:38461418
|
G | A | 17 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0158others(14): Show | 17 | HG00733.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-15797C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461418 | ||||||
| chr21:38461568
|
G | T | 278 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(275): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.19-15947C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461568 | ||||||
| chr21:38461646
|
T | C | 267 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.19-16025A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461646 | ||||||
| chr21:38461694
|
G | T | 1 | a0001c0001t0002g0341 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.19-16073C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461694 | ||||||
| chr21:38461749
|
T | C | 1 | a0001c0001t0008g0214 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.19-16128A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461749 | ||||||
| chr21:38461772
|
T | C | 2 | a0001c0001t0001g0344a0001c0001t0002g0345 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.19-16151A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461772 | ||||||
| chr21:38461845
|
C | T | 158 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(155): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.19-16224G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461845 | ||||||
| chr21:38461890
|
C | T | 18 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.19-16269G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461890 | ||||||
| chr21:38461971
|
A | AT | 10 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0001g0210others(7): Show | 10 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-16351dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461971 | ||||||
| chr21:38461971
|
A | T | 1 | a0001c0001t0005g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-16350T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38461971 | ||||||
| chr21:38462045
|
G | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0292a0001c0001t0001g0353others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-16424C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462045 | ||||||
| chr21:38462056
|
A | G | 3 | a0001c0001t0001g0281a0001c0001t0011g0320a0001c0001t0030g0256 | 3 | HG02109.hp1 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.19-16435T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462056 | ||||||
| chr21:38462124
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0234a0001c0001t0002g0235 | 3 | HG00639.hp1 HG01070.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.19-16503C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462124 | ||||||
| chr21:38462332
|
CT | C | 29 | a0001c0001t0001g0114a0001c0001t0001g0145a0001c0001t0001g0147others(26): Show | 29 | HG00597.hp2 HG01074.hp2 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-16712delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462332 | ||||||
| chr21:38462372
|
AT | A | 239 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(236): Show | 241 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.19-16752delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462372 | ||||||
| chr21:38462387
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.19-16766A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462387 | ||||||
| chr21:38462407
|
C | T | 265 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(262): Show | 267 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.19-16786G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462407 | ||||||
| chr21:38462661
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.19-17040A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462661 | ||||||
| chr21:38462738
|
C | A | 9 | a0001c0001t0001g0143a0001c0001t0001g0292a0001c0001t0001g0353others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-17117G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462738 | ||||||
| chr21:38462739
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.19-17118C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462739 | ||||||
| chr21:38462863
|
G | A | 1 | a0001c0001t0024g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.19-17242C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462863 | ||||||
| chr21:38462869
|
C | G | 64 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(61): Show | 64 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.19-17248G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38462869 | ||||||
| chr21:38463103
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.19-17482T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463103 | ||||||
| chr21:38463108
|
T | C | 53 | a0001c0001t0001g0061a0001c0001t0001g0101a0001c0001t0001g0191others(50): Show | 53 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.19-17487A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463108 | ||||||
| chr21:38463164
|
T | A | 55 | a0001c0001t0001g0061a0001c0001t0001g0101a0001c0001t0001g0191others(52): Show | 55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.19-17543A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463164 | ||||||
| chr21:38463203
|
G | C | 12 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0112others(9): Show | 12 | HG00733.hp1 HG02080.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.19-17582C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463203 | ||||||
| chr21:38463238
|
T | C | 59 | a0001c0001t0001g0065a0001c0001t0001g0119a0001c0001t0001g0165others(56): Show | 61 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.19-17617A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463238 | ||||||
| chr21:38463275
|
T | C | 46 | a0001c0001t0001g0211a0001c0001t0001g0253a0001c0001t0001g0255others(43): Show | 46 | HG00639.hp2 HG00735.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-17654A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463275 | ||||||
| chr21:38463297
|
T | G | 2 | a0001c0001t0001g0278a0001c0001t0011g0279 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.19-17676A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463297 | ||||||
| chr21:38463349
|
C | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 4 | NA18942.hp2 NA18943.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-17728G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463349 | ||||||
| chr21:38463363
|
T | C | 320 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.19-17742A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463363 | ||||||
| chr21:38463375
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-17754T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463375 | ||||||
| chr21:38463475
|
A | G | 1 | a0001c0001t0003g0308 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.19-17854T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463475 | ||||||
| chr21:38463567
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.19-17946G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463567 | ||||||
| chr21:38463863
|
T | G | 2 | a0001c0002t0012g0228a0001c0002t0012g0294 | 2 | HG01361.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19-18242A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463863 | ||||||
| chr21:38463877
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19-18256A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463877 | ||||||
| chr21:38463966
|
G | A | 2 | a0001c0001t0003g0222a0001c0001t0003g0223 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.19-18345C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38463966 | ||||||
| chr21:38464034
|
T | C | 13 | a0001c0001t0001g0127a0001c0001t0001g0344a0001c0001t0002g0121others(10): Show | 13 | HG01106.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.19-18413A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38464034 | ||||||
| chr21:38464281
|
G | A | 52 | a0001c0001t0001g0061a0001c0001t0001g0101a0001c0001t0001g0191others(49): Show | 52 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.19-18660C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38464281 | ||||||
| chr21:38464436
|
A | G | 3 | a0001c0001t0002g0134a0001c0001t0011g0205a0001c0001t0030g0256 | 3 | HG00735.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.19-18815T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38464436 | ||||||
| chr21:38464527
|
G | C | 2 | a0001c0001t0006g0036a0001c0001t0015g0037 | 2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.19-18906C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38464527 | ||||||
| chr21:38464724
|
C | T | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.19-19103G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38464724 | ||||||
| chr21:38464727
|
C | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.19-19106G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38464727 | ||||||
| chr21:38464781
|
A | C | 9 | a0001c0001t0001g0309a0001c0001t0001g0316a0001c0001t0002g0299others(6): Show | 9 | HG01981.hp1 HG02080.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-19160T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38464781 | ||||||
| chr21:38464969
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0011g0279 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.19-19348C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38464969 | ||||||
| chr21:38465179
|
T | C | 1 | a0001c0001t0020g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.19-19558A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465179 | ||||||
| chr21:38465223
|
T | G | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(14): Show | 17 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-19602A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465223 | ||||||
| chr21:38465463
|
T | A | 71 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.19-19842A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465463 | ||||||
| chr21:38465560
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.19-19939C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465560 | ||||||
| chr21:38465567
|
A | G | 1 | a0001c0001t0001g0354 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.19-19946T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465567 | ||||||
| chr21:38465667
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0011g0279 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.19-20046C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465667 | ||||||
| chr21:38465700
|
G | A | 108 | a0001c0001t0001g0101a0001c0001t0001g0145a0001c0001t0001g0147others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.19-20079C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465700 | ||||||
| chr21:38465759
|
A | G | 14 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0112others(11): Show | 14 | HG00733.hp1 HG02080.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-20138T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465759 | ||||||
| chr21:38465855
|
G | T | 3 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0002g0254 | 3 | HG02258.hp1 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-20234C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465855 | ||||||
| chr21:38465883
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19-20262C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38465883 | ||||||
| chr21:38466112
|
T | A | 95 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(92): Show | 96 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.19-20491A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466112 | ||||||
| chr21:38466124
|
G | C | 1 | a0001c0001t0003g0337 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.19-20503C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466124 | ||||||
| chr21:38466134
|
T | C | 116 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(113): Show | 116 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.19-20513A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466134 | ||||||
| chr21:38466300
|
G | GGGGTGT | 28 | a0001c0001t0001g0309a0001c0001t0001g0311a0001c0001t0001g0312others(25): Show | 28 | HG00639.hp2 HG01099.hp2 HG01981.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-20680_19-20679i others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGGGTGTG others(3): Show |
1 | a0001c0001t0007g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.19-20680_19-20679i others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGGGTGTG others(5): Show |
2 | a0001c0001t0001g0184a0001c0001t0003g0188 | 2 | HG00642.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.19-20680_19-20679i others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGT | 86 | a0001c0001t0001g0061a0001c0001t0001g0101a0001c0001t0001g0119others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.19-20681_19-20680d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGT | 11 | a0001c0001t0001g0211a0001c0001t0001g0259a0001c0001t0001g0264others(8): Show | 11 | HG00735.hp1 HG01361.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-20685_19-20680d others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0001g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.19-20680_19-20679i others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(3): Show |
3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0003g0131 | 3 | HG02132.hp2 NA18747.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.19-20680_19-20679i others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(5): Show |
2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02056.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.19-20680_19-20679i others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(7): Show |
9 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0137others(6): Show | 9 | HG02027.hp2 NA18955.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-20680_19-20679i others(16): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(8): Show |
1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.19-20680_19-20679i others(17): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(1): Show |
24 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0001g0074others(21): Show | 24 | HG00438.hp1 HG01081.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.19-20687_19-20680d others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(3): Show |
8 | a0001c0001t0001g0080a0001c0001t0001g0114a0001c0001t0001g0186others(5): Show | 9 | HG01074.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-20689_19-20680d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(5): Show |
50 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0064others(47): Show | 50 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.19-20691_19-20680d others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(7): Show |
15 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0099others(12): Show | 15 | HG00673.hp1 HG01070.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-20693_19-20680d others(16): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(9): Show |
8 | a0001c0001t0001g0143a0001c0001t0001g0187a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-20695_19-20680d others(18): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(11): Show |
1 | a0001c0001t0001g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.19-20697_19-20680d others(20): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GGTGTGTG others(13): Show |
2 | a0001c0001t0003g0342a0001c0001t0003g0343 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.19-20699_19-20680d others(22): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GTGTGTGT others(6): Show |
2 | a0001c0001t0001g0175a0001c0001t0002g0166 | 2 | HG02602.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.19-20680_19-20679i others(15): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466300
|
G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.19-20680_19-20679i others(17): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466300 | ||||||
| chr21:38466302
|
T | G | 1 | a0001c0001t0030g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.19-20681A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466302 | ||||||
| chr21:38466365
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.19-20744A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466365 | ||||||
| chr21:38466392
|
C | A | 8 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(5): Show | 8 | HG00609.hp2 HG02056.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-20771G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466392 | ||||||
| chr21:38466468
|
T | G | 1 | a0001c0001t0010g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.19-20847A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466468 | ||||||
| chr21:38466476
|
A | G | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0006t0001g0177 | 3 | HG02602.hp1 HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.19-20855T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466476 | ||||||
| chr21:38466516
|
G | C | 9 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-20895C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466516 | ||||||
| chr21:38466649
|
T | C | 277 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.19-21028A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466649 | ||||||
| chr21:38466813
|
T | C | 15 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-21192A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466813 | ||||||
| chr21:38466871
|
A | T | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(14): Show | 17 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-21250T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466871 | ||||||
| chr21:38466902
|
C | T | 64 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0286others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.19-21281G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38466902 | ||||||
| chr21:38467042
|
C | T | 15 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-21421G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467042 | ||||||
| chr21:38467075
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-21454G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467075 | ||||||
| chr21:38467102
|
T | C | 4 | a0001c0001t0001g0119a0001c0001t0004g0012a0001c0001t0004g0044others(1): Show | 4 | HG00558.hp1 HG00609.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-21481A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467102 | ||||||
| chr21:38467128
|
A | G | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-21507T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467128 | ||||||
| chr21:38467284
|
A | G | 15 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-21663T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467284 | ||||||
| chr21:38467317
|
GCCTCAAA others(4): Show |
G | 47 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(44): Show | 47 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.19-21707_19-21697d others(13): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467317 | ||||||
| chr21:38467572
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.19-21951C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467572 | ||||||
| chr21:38467603
|
T | C | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-21982A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467603 | ||||||
| chr21:38467620
|
G | A | 8 | a0001c0001t0001g0127a0001c0001t0002g0121a0001c0001t0002g0122others(5): Show | 8 | HG00673.hp2 HG01106.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-21999C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467620 | ||||||
| chr21:38467663
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.19-22042A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467663 | ||||||
| chr21:38467934
|
T | C | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-22313A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38467934 | ||||||
| chr21:38468040
|
T | C | 2 | a0001c0001t0002g0304a0001c0001t0003g0298 | 2 | NA19009.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.19-22419A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468040 | ||||||
| chr21:38468195
|
C | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-22574G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468195 | ||||||
| chr21:38468313
|
C | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-22692G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468313 | ||||||
| chr21:38468521
|
C | G | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-22900G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468521 | ||||||
| chr21:38468547
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.19-22926T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468547 | ||||||
| chr21:38468752
|
G | A | 2 | a0001c0001t0004g0040a0001c0001t0023g0339 | 2 | HG00099.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.19-23131C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468752 | ||||||
| chr21:38468781
|
C | T | 35 | a0001c0001t0001g0065a0001c0001t0001g0165a0001c0001t0001g0167others(32): Show | 36 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.19-23160G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468781 | ||||||
| chr21:38468782
|
G | A | 1 | a0001c0001t0002g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.19-23161C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468782 | ||||||
| chr21:38468842
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG01257.hp2 HG01258.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.19-23221C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468842 | ||||||
| chr21:38468846
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0011g0205 | 2 | HG00735.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.19-23225C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468846 | ||||||
| chr21:38468901
|
C | T | 8 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(5): Show | 8 | HG00609.hp2 HG02056.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-23280G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468901 | ||||||
| chr21:38468902
|
G | A | 14 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(11): Show | 14 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-23281C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468902 | ||||||
| chr21:38468926
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.19-23305T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468926 | ||||||
| chr21:38468940
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0003g0160 | 2 | HG01081.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.19-23319C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468940 | ||||||
| chr21:38468982
|
C | CA | 12 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0283others(9): Show | 12 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.19-23362dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468982 | ||||||
| chr21:38468982
|
C | CAAAAAAA | 6 | a0001c0001t0001g0193a0001c0001t0001g0197a0001c0001t0002g0002others(3): Show | 7 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-23368_19-23362d others(9): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468982 | ||||||
| chr21:38468982
|
C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0176others(11): Show | 14 | HG00597.hp1 HG02074.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-23369_19-23362d others(10): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468982 | ||||||
| chr21:38468982
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0184a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG00438.hp1 HG00642.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.19-23370_19-23362d others(11): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468982 | ||||||
| chr21:38468982
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0165 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.19-23371_19-23362d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468982 | ||||||
| chr21:38468985
|
AAAAAAAA others(10): Show |
A | 46 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(43): Show | 46 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-23381_19-23365d others(19): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468985 | ||||||
| chr21:38468986
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0003g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.19-23381_19-23366d others(18): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468986 | ||||||
| chr21:38468991
|
AAAAAAAA others(4): Show |
A | 6 | a0001c0001t0001g0065a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG02809.hp1 HG02809.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-23381_19-23371d others(13): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468991 | ||||||
| chr21:38468992
|
AAAAAAAA others(3): Show |
A | 5 | a0001c0001t0001g0186a0001c0001t0001g0292a0001c0001t0002g0185others(2): Show | 5 | HG01346.hp2 HG03486.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-23381_19-23372d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468992 | ||||||
| chr21:38468997
|
A | G | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG00544.hp2 HG02027.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-23376T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38468997 | ||||||
| chr21:38469002
|
G | A | 39 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0175others(36): Show | 40 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.19-23381C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469002 | ||||||
| chr21:38469002
|
GA | G | 40 | a0001c0001t0001g0211a0001c0001t0001g0259a0001c0001t0001g0264others(37): Show | 40 | HG00639.hp2 HG01099.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.19-23382delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469002 | ||||||
| chr21:38469003
|
A | G | 5 | a0001c0001t0001g0318a0001c0001t0001g0327a0001c0001t0002g0299others(2): Show | 5 | HG02071.hp2 HG02683.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-23382T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469003 | ||||||
| chr21:38469054
|
C | CA | 10 | a0001c0001t0001g0077a0001c0001t0001g0105a0001c0001t0001g0211others(7): Show | 10 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-23434dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469054 | ||||||
| chr21:38469054
|
CA | C | 8 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(5): Show | 8 | HG00609.hp2 HG02056.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-23434delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469054 | ||||||
| chr21:38469074
|
C | T | 1 | a0001c0003t0010g0251 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.19-23453G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469074 | ||||||
| chr21:38469174
|
C | A | 5 | a0001c0001t0001g0211a0001c0001t0001g0259a0001c0001t0001g0264others(2): Show | 5 | HG01975.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-23553G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469174 | ||||||
| chr21:38469267
|
A | G | 2 | a0001c0001t0002g0182a0001c0002t0012g0181 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.19-23646T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469267 | ||||||
| chr21:38469290
|
G | T | 1 | a0001c0001t0003g0270 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.19-23669C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469290 | ||||||
| chr21:38469339
|
T | C | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(14): Show | 17 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-23718A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469339 | ||||||
| chr21:38469366
|
C | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00609.hp2 HG02056.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-23745G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469366 | ||||||
| chr21:38469391
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.19-23770A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469391 | ||||||
| chr21:38469429
|
C | A | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.19-23808G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469429 | ||||||
| chr21:38469454
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19-23833G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469454 | ||||||
| chr21:38469476
|
A | G | 47 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(44): Show | 47 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.19-23855T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469476 | ||||||
| chr21:38469492
|
C | T | 1 | a0001c0001t0004g0025 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.19-23871G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469492 | ||||||
| chr21:38469549
|
T | TAAC | 14 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(11): Show | 14 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-23931_19-23929d others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469549 | ||||||
| chr21:38469671
|
A | C | 1 | a0001c0001t0002g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-24050T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469671 | ||||||
| chr21:38469908
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0011g0279 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.19-24287C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38469908 | ||||||
| chr21:38470043
|
C | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0285others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-24422G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470043 | ||||||
| chr21:38470050
|
G | C | 74 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0128others(71): Show | 75 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.19-24429C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470050 | ||||||
| chr21:38470099
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.19-24478A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470099 | ||||||
| chr21:38470257
|
CTAT | C | 227 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(224): Show | 228 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.19-24639_19-24637d others(5): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470257 | ||||||
| chr21:38470257
|
CTATTAT | C | 15 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(12): Show | 15 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-24642_19-24637d others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470257 | ||||||
| chr21:38470257
|
CTATTATT others(5): Show |
C | 81 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0128others(78): Show | 82 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.19-24648_19-24637d others(14): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470257 | ||||||
| chr21:38470326
|
G | T | 53 | a0001c0001t0001g0061a0001c0001t0001g0158a0001c0001t0001g0159others(50): Show | 53 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.19-24705C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470326 | ||||||
| chr21:38470355
|
A | G | 8 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(5): Show | 8 | HG00609.hp2 HG02056.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-24734T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470355 | ||||||
| chr21:38470360
|
C | T | 1 | a0001c0001t0003g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.19-24739G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470360 | ||||||
| chr21:38470445
|
T | G | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-24824A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470445 | ||||||
| chr21:38470614
|
G | T | 1 | a0001c0001t0001g0218 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.19-24993C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470614 | ||||||
| chr21:38470638
|
A | G | 1 | a0001c0001t0001g0340 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.19-25017T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470638 | ||||||
| chr21:38470722
|
T | C | 6 | a0001c0001t0001g0119a0001c0001t0004g0012a0001c0001t0004g0044others(3): Show | 6 | HG00558.hp1 HG00609.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-25101A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470722 | ||||||
| chr21:38470808
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.19-25187C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38470808 | ||||||
| chr21:38471020
|
G | T | 16 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(13): Show | 16 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.19-25399C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471020 | ||||||
| chr21:38471075
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19-25454T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471075 | ||||||
| chr21:38471118
|
G | A | 7 | a0001c0001t0001g0127a0001c0001t0002g0121a0001c0001t0002g0122others(4): Show | 7 | HG01106.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-25497C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471118 | ||||||
| chr21:38471160
|
G | A | 65 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0286others(62): Show | 66 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.19-25539C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471160 | ||||||
| chr21:38471165
|
G | A | 5 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0357others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-25544C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471165 | ||||||
| chr21:38471260
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.19-25639A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471260 | ||||||
| chr21:38471370
|
G | C | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-25749C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471370 | ||||||
| chr21:38471469
|
C | T | 274 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(271): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.19-25848G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471469 | ||||||
| chr21:38471539
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.19-25918G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471539 | ||||||
| chr21:38471540
|
G | A | 1 | a0001c0001t0002g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.19-25919C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471540 | ||||||
| chr21:38471563
|
T | G | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-25942A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471563 | ||||||
| chr21:38471639
|
AT | A | 5 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0357others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-26019delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471639 | ||||||
| chr21:38471914
|
C | T | 1 | a0001c0001t0006g0046 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.19-26293G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471914 | ||||||
| chr21:38471973
|
C | T | 1 | a0001c0001t0004g0016 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.19-26352G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38471973 | ||||||
| chr21:38472301
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.18+26062A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38472301 | ||||||
| chr21:38472308
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0002g0081others(2): Show | 5 | NA18959.hp2 NA19011.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+26055C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38472308 | ||||||
| chr21:38472402
|
C | G | 1 | a0001c0001t0003g0100 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.18+25961G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38472402 | ||||||
| chr21:38472637
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.18+25726G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38472637 | ||||||
| chr21:38472640
|
T | C | 1 | a0001c0001t0002g0328 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.18+25723A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38472640 | ||||||
| chr21:38472799
|
C | T | 1 | a0001c0001t0006g0038 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.18+25564G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38472799 | ||||||
| chr21:38472865
|
C | G | 88 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0128others(85): Show | 89 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.18+25498G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38472865 | ||||||
| chr21:38472978
|
G | A | 15 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(12): Show | 15 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+25385C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38472978 | ||||||
| chr21:38473010
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.18+25353C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473010 | ||||||
| chr21:38473032
|
A | G | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+25331T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473032 | ||||||
| chr21:38473059
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0285others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+25304G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473059 | ||||||
| chr21:38473107
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+25256T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473107 | ||||||
| chr21:38473117
|
C | T | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+25246G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473117 | ||||||
| chr21:38473155
|
C | T | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+25208G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473155 | ||||||
| chr21:38473159
|
C | CA | 17 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0107others(14): Show | 17 | HG00733.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.18+25203dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473159 | ||||||
| chr21:38473159
|
CA | C | 172 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0101others(169): Show | 174 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.18+25203delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473159 | ||||||
| chr21:38473159
|
CAA | C | 65 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(62): Show | 65 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.18+25202_18+25203d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473159 | ||||||
| chr21:38473180
|
G | A | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+25183C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473180 | ||||||
| chr21:38473317
|
G | A | 319 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.18+25046C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473317 | ||||||
| chr21:38473352
|
T | C | 15 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0107others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+25011A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473352 | ||||||
| chr21:38473426
|
C | CAT | 6 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+24935_18+24936d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473426 | ||||||
| chr21:38473426
|
C | CATAT | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+24933_18+24936d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473426 | ||||||
| chr21:38473426
|
CAT | C | 75 | a0001c0001t0001g0127a0001c0001t0001g0145a0001c0001t0001g0147others(72): Show | 75 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.18+24935_18+24936d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473426 | ||||||
| chr21:38473669
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.18+24694G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473669 | ||||||
| chr21:38473704
|
G | GTTATAC | 9 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+24658_18+24659i others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473704 | ||||||
| chr21:38473750
|
T | C | 1 | a0001c0001t0002g0324 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.18+24613A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473750 | ||||||
| chr21:38473794
|
A | ATATG | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+24568_18+24569i others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473794 | ||||||
| chr21:38473794
|
ATG | A | 90 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(87): Show | 91 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.18+24567_18+24568d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473794 | ||||||
| chr21:38473826
|
G | A | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+24537C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473826 | ||||||
| chr21:38473858
|
G | A | 1 | a0001c0001t0007g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.18+24505C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473858 | ||||||
| chr21:38473893
|
TGTAA | T | 9 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+24466_18+24469d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473893 | ||||||
| chr21:38473965
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.18+24398T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38473965 | ||||||
| chr21:38474017
|
G | T | 64 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0286others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+24346C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38474017 | ||||||
| chr21:38474047
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.18+24316C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38474047 | ||||||
| chr21:38474219
|
G | A | 64 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0286others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+24144C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38474219 | ||||||
| chr21:38474348
|
G | GCGACA | 64 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0286others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+24010_18+24014d others(7): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38474348 | ||||||
| chr21:38474524
|
C | T | 1 | a0001c0001t0010g0192 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+23839G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38474524 | ||||||
| chr21:38474731
|
AT | A | 326 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(323): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.18+23631delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38474731 | ||||||
| chr21:38474731
|
ATT | A | 10 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0126others(7): Show | 10 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+23630_18+23631d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38474731 | ||||||
| chr21:38474772
|
G | A | 55 | a0001c0001t0001g0061a0001c0001t0001g0158a0001c0001t0001g0159others(52): Show | 55 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.18+23591C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38474772 | ||||||
| chr21:38475120
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.18+23243C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475120 | ||||||
| chr21:38475121
|
C | T | 8 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(5): Show | 8 | HG00609.hp2 HG02056.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+23242G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475121 | ||||||
| chr21:38475122
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.18+23241C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475122 | ||||||
| chr21:38475204
|
C | T | 1 | a0001c0001t0004g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.18+23159G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475204 | ||||||
| chr21:38475356
|
A | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.18+23007T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475356 | ||||||
| chr21:38475571
|
A | T | 3 | a0001c0001t0001g0167a0001c0001t0002g0166a0001c0001t0005g0003 | 3 | HG02523.hp2 NA18612.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.18+22792T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475571 | ||||||
| chr21:38475639
|
T | C | 170 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(167): Show | 172 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.18+22724A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475639 | ||||||
| chr21:38475640
|
G | A | 6 | a0001c0001t0001g0191a0001c0001t0001g0200a0001c0001t0003g0198others(3): Show | 6 | HG00738.hp1 HG01074.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+22723C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475640 | ||||||
| chr21:38475793
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+22570A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38475793 | ||||||
| chr21:38476339
|
G | C | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+22024C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476339 | ||||||
| chr21:38476390
|
G | A | 1 | a0001c0001t0002g0225 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.18+21973C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476390 | ||||||
| chr21:38476396
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0011g0279 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.18+21967G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476396 | ||||||
| chr21:38476447
|
G | A | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+21916C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476447 | ||||||
| chr21:38476577
|
G | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+21786C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476577 | ||||||
| chr21:38476616
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.18+21747G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476616 | ||||||
| chr21:38476652
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0250 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.18+21711T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476652 | ||||||
| chr21:38476656
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.18+21707C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476656 | ||||||
| chr21:38476707
|
C | A | 64 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0286others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+21656G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476707 | ||||||
| chr21:38476707
|
C | T | 38 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(35): Show | 38 | HG00544.hp2 HG00597.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.18+21656G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476707 | ||||||
| chr21:38476790
|
G | A | 7 | a0001c0001t0001g0127a0001c0001t0002g0121a0001c0001t0002g0122others(4): Show | 7 | HG01106.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+21573C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476790 | ||||||
| chr21:38476843
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.18+21520C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476843 | ||||||
| chr21:38476868
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.18+21495C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476868 | ||||||
| chr21:38476948
|
T | C | 5 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0357others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+21415A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476948 | ||||||
| chr21:38476982
|
G | T | 357 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(354): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.18+21381C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38476982 | ||||||
| chr21:38477007
|
C | CT | 218 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0064others(215): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.18+21355dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477007 | ||||||
| chr21:38477007
|
C | CTT | 20 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0082others(17): Show | 20 | HG00597.hp1 HG00597.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+21354_18+21355d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477007 | ||||||
| chr21:38477007
|
CT | C | 6 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0285others(3): Show | 6 | HG00639.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+21355delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477007 | ||||||
| chr21:38477038
|
A | G | 45 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0172others(42): Show | 46 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.18+21325T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477038 | ||||||
| chr21:38477043
|
C | A | 55 | a0001c0001t0001g0061a0001c0001t0001g0158a0001c0001t0001g0159others(52): Show | 55 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.18+21320G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477043 | ||||||
| chr21:38477284
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.18+21079C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477284 | ||||||
| chr21:38477296
|
G | A | 1 | a0001c0001t0002g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+21067C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477296 | ||||||
| chr21:38477334
|
T | A | 1 | a0001c0001t0001g0290 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.18+21029A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477334 | ||||||
| chr21:38477427
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.18+20936A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477427 | ||||||
| chr21:38477462
|
C | G | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+20901G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477462 | ||||||
| chr21:38477630
|
T | G | 64 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0286others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+20733A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477630 | ||||||
| chr21:38477965
|
T | C | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+20398A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477965 | ||||||
| chr21:38477994
|
C | T | 62 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(59): Show | 62 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.18+20369G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38477994 | ||||||
| chr21:38478072
|
T | C | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+20291A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478072 | ||||||
| chr21:38478082
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+20281G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478082 | ||||||
| chr21:38478121
|
C | T | 3 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301 | 3 | NA18988.hp2 NA19056.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.18+20242G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478121 | ||||||
| chr21:38478236
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.18+20127C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478236 | ||||||
| chr21:38478242
|
G | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0163a0001c0001t0003g0162 | 3 | HG02602.hp2 HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.18+20121C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478242 | ||||||
| chr21:38478435
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.18+19928G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478435 | ||||||
| chr21:38478436
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.18+19927A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478436 | ||||||
| chr21:38478437
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.18+19926G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478437 | ||||||
| chr21:38478449
|
G | T | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.18+19914C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478449 | ||||||
| chr21:38478631
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.18+19732C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478631 | ||||||
| chr21:38478716
|
A | C | 39 | a0001c0001t0001g0306a0001c0001t0001g0309a0001c0001t0001g0311others(36): Show | 39 | HG00639.hp2 HG01099.hp2 HG02071.hp2 others(36): Show |
intron_variant | MODIFIER | c.18+19647T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478716 | ||||||
| chr21:38478786
|
G | C | 61 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0289others(58): Show | 62 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.18+19577C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478786 | ||||||
| chr21:38478849
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.18+19514G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478849 | ||||||
| chr21:38478973
|
C | A | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.18+19390G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478973 | ||||||
| chr21:38478998
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.18+19365G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38478998 | ||||||
| chr21:38479032
|
C | A | 15 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0107others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+19331G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38479032 | ||||||
| chr21:38479039
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.18+19324T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38479039 | ||||||
| chr21:38479260
|
A | C | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+19103T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38479260 | ||||||
| chr21:38479587
|
G | T | 1 | a0001c0001t0004g0020 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.18+18776C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38479587 | ||||||
| chr21:38479755
|
AC | A | 66 | a0001c0001t0001g0119a0001c0001t0001g0286a0001c0001t0001g0287others(63): Show | 67 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.18+18607delG | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38479755 | ||||||
| chr21:38480061
|
C | A | 1 | a0003c0005t0001g0102 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.18+18302G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480061 | ||||||
| chr21:38480086
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0236a0001c0001t0001g0250 | 3 | HG01433.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.18+18277G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480086 | ||||||
| chr21:38480156
|
G | A | 59 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.18+18207C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480156 | ||||||
| chr21:38480218
|
G | A | 1 | a0001c0001t0007g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.18+18145C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480218 | ||||||
| chr21:38480355
|
C | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0002g0141others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+18008G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480355 | ||||||
| chr21:38480473
|
C | A | 270 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(267): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.18+17890G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480473 | ||||||
| chr21:38480530
|
TA | T | 274 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(271): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.18+17832delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480530 | ||||||
| chr21:38480549
|
T | C | 67 | a0001c0001t0001g0119a0001c0001t0001g0286a0001c0001t0001g0287others(64): Show | 68 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.18+17814A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480549 | ||||||
| chr21:38480591
|
C | CT | 14 | a0001c0001t0001g0129a0001c0001t0001g0159a0001c0001t0001g0231others(11): Show | 14 | HG00639.hp1 HG01081.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+17771dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480591 | ||||||
| chr21:38480591
|
C | CTTTT | 58 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0112others(55): Show | 58 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.18+17768_18+17771d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480591 | ||||||
| chr21:38480591
|
C | CTTTTT | 34 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0108others(31): Show | 34 | HG00735.hp1 HG01070.hp2 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.18+17767_18+17771d others(7): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480591 | ||||||
| chr21:38480591
|
C | CTTTTTT | 61 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0066others(58): Show | 62 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.18+17766_18+17771d others(8): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480591 | ||||||
| chr21:38480591
|
C | CTTTTTTT | 31 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0072others(28): Show | 31 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.18+17765_18+17771d others(9): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480591 | ||||||
| chr21:38480591
|
CT | C | 11 | a0001c0001t0001g0127a0001c0001t0001g0143a0001c0001t0001g0153others(8): Show | 11 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.18+17771delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480591 | ||||||
| chr21:38480591
|
CTTTT | C | 64 | a0001c0001t0001g0119a0001c0001t0001g0286a0001c0001t0001g0287others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+17768_18+17771d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480591 | ||||||
| chr21:38480591
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.18+17762_18+17771d others(12): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480591 | ||||||
| chr21:38480597
|
T | G | 1 | a0001c0002t0012g0228 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.18+17766A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480597 | ||||||
| chr21:38480628
|
A | T | 15 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0107others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+17735T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480628 | ||||||
| chr21:38480631
|
T | A | 1 | a0001c0006t0001g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.18+17732A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480631 | ||||||
| chr21:38480963
|
T | C | 1 | a0001c0001t0016g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+17400A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38480963 | ||||||
| chr21:38481344
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.18+17019G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38481344 | ||||||
| chr21:38481413
|
T | C | 83 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(80): Show | 83 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.18+16950A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38481413 | ||||||
| chr21:38481562
|
A | G | 15 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0107others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+16801T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38481562 | ||||||
| chr21:38481639
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0002g0166 | 2 | HG02523.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.18+16724G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38481639 | ||||||
| chr21:38481730
|
A | G | 3 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0002g0254 | 3 | HG02258.hp1 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+16633T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38481730 | ||||||
| chr21:38481765
|
T | C | 67 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(64): Show | 68 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.18+16598A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38481765 | ||||||
| chr21:38481934
|
T | C | 325 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+16429A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38481934 | ||||||
| chr21:38481968
|
A | G | 1 | a0001c0001t0016g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+16395T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38481968 | ||||||
| chr21:38482000
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.18+16363A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482000 | ||||||
| chr21:38482060
|
G | A | 1 | a0001c0001t0020g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.18+16303C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482060 | ||||||
| chr21:38482337
|
A | T | 66 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(63): Show | 67 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.18+16026T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482337 | ||||||
| chr21:38482555
|
C | T | 15 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0107others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+15808G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482555 | ||||||
| chr21:38482557
|
C | G | 1 | a0001c0001t0002g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+15806G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482557 | ||||||
| chr21:38482587
|
A | G | 66 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(63): Show | 67 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.18+15776T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482587 | ||||||
| chr21:38482683
|
C | CT | 89 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0128others(86): Show | 90 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.18+15679dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482683 | ||||||
| chr21:38482760
|
C | G | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+15603G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482760 | ||||||
| chr21:38482866
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.18+15497G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482866 | ||||||
| chr21:38482870
|
C | G | 66 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(63): Show | 67 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.18+15493G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482870 | ||||||
| chr21:38482903
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.18+15460G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38482903 | ||||||
| chr21:38483074
|
A | G | 66 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(63): Show | 67 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.18+15289T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483074 | ||||||
| chr21:38483215
|
A | G | 16 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(13): Show | 16 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.18+15148T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483215 | ||||||
| chr21:38483239
|
G | A | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+15124C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483239 | ||||||
| chr21:38483279
|
T | C | 4 | a0001c0001t0001g0323a0001c0001t0002g0322a0001c0001t0003g0321others(1): Show | 4 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+15084A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483279 | ||||||
| chr21:38483427
|
T | C | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+14936A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483427 | ||||||
| chr21:38483566
|
C | T | 3 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0002g0254 | 3 | HG02258.hp1 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+14797G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483566 | ||||||
| chr21:38483690
|
T | TACAA | 25 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(22): Show | 25 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.18+14669_18+14672d others(6): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483690 | ||||||
| chr21:38483711
|
A | T | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.18+14652T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483711 | ||||||
| chr21:38483736
|
G | A | 61 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(58): Show | 61 | HG00099.hp1 HG00597.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.18+14627C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483736 | ||||||
| chr21:38483800
|
G | A | 1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.18+14563C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483800 | ||||||
| chr21:38483829
|
A | T | 65 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(62): Show | 66 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+14534T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483829 | ||||||
| chr21:38483958
|
A | G | 1 | a0001c0001t0031g0358 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.18+14405T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38483958 | ||||||
| chr21:38484091
|
A | T | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+14272T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484091 | ||||||
| chr21:38484124
|
C | T | 1 | a0001c0001t0003g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.18+14239G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484124 | ||||||
| chr21:38484130
|
A | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG00544.hp2 NA18959.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+14233T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484130 | ||||||
| chr21:38484279
|
T | A | 15 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0107others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+14084A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484279 | ||||||
| chr21:38484319
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+14044A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484319 | ||||||
| chr21:38484492
|
G | A | 65 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(62): Show | 66 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+13871C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484492 | ||||||
| chr21:38484519
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.18+13844A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484519 | ||||||
| chr21:38484631
|
T | A | 65 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(62): Show | 66 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+13732A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484631 | ||||||
| chr21:38484974
|
T | G | 15 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0107others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+13389A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38484974 | ||||||
| chr21:38485068
|
A | C | 319 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.18+13295T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485068 | ||||||
| chr21:38485156
|
A | G | 5 | a0001c0001t0004g0010a0001c0001t0004g0016a0001c0001t0004g0017others(2): Show | 5 | NA18939.hp1 NA18970.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+13207T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485156 | ||||||
| chr21:38485177
|
A | G | 65 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(62): Show | 66 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+13186T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485177 | ||||||
| chr21:38485234
|
A | C | 5 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0357others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+13129T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485234 | ||||||
| chr21:38485252
|
TA | T | 162 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0105others(159): Show | 162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.18+13110delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485252 | ||||||
| chr21:38485252
|
TAA | T | 64 | a0001c0001t0001g0107a0001c0001t0001g0119a0001c0001t0001g0286others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+13109_18+13110d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485252 | ||||||
| chr21:38485325
|
A | G | 329 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(326): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.18+13038T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485325 | ||||||
| chr21:38485352
|
C | T | 1 | a0001c0001t0021g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.18+13011G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485352 | ||||||
| chr21:38485401
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.18+12962T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485401 | ||||||
| chr21:38485461
|
C | CT | 62 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(59): Show | 62 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.18+12901dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485461 | ||||||
| chr21:38485461
|
CT | C | 66 | a0001c0001t0001g0065a0001c0001t0001g0107a0001c0001t0001g0108others(63): Show | 67 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.18+12901delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485461 | ||||||
| chr21:38485473
|
T | TC | 8 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(5): Show | 8 | HG00544.hp2 HG02027.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+12889_18+12890i others(3): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485473 | ||||||
| chr21:38485493
|
C | T | 15 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(12): Show | 15 | HG00609.hp2 HG01106.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+12870G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485493 | ||||||
| chr21:38485608
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.18+12755G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485608 | ||||||
| chr21:38485620
|
C | T | 64 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+12743G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485620 | ||||||
| chr21:38485620
|
CGGCTAAT others(467): Show |
C | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+12269_18+12742d others(2): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485620 | ||||||
| chr21:38485705
|
A | G | 65 | a0001c0001t0001g0119a0001c0001t0001g0285a0001c0001t0001g0286others(62): Show | 66 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+12658T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485705 | ||||||
| chr21:38485748
|
G | A | 5 | a0001c0001t0001g0127a0001c0001t0002g0123a0001c0001t0002g0124others(2): Show | 5 | HG01106.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+12615C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485748 | ||||||
| chr21:38485831
|
G | T | 2 | a0001c0001t0002g0182a0001c0002t0012g0181 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.18+12532C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485831 | ||||||
| chr21:38485853
|
C | T | 2 | a0001c0001t0003g0229a0001c0001t0003g0230 | 2 | HG00280.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.18+12510G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485853 | ||||||
| chr21:38485910
|
T | C | 317 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(314): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.18+12453A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38485910 | ||||||
| chr21:38486080
|
C | T | 1 | a0001c0002t0012g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.18+12283G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486080 | ||||||
| chr21:38486108
|
T | C | 7 | a0001c0001t0001g0127a0001c0001t0002g0121a0001c0001t0002g0122others(4): Show | 7 | HG01106.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+12255A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486108 | ||||||
| chr21:38486131
|
C | T | 2 | a0001c0001t0003g0342a0001c0001t0003g0343 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.18+12232G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486131 | ||||||
| chr21:38486140
|
A | G | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+12223T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486140 | ||||||
| chr21:38486155
|
C | G | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+12208G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486155 | ||||||
| chr21:38486163
|
G | A | 4 | a0001c0001t0001g0119a0001c0001t0004g0012a0001c0001t0004g0044others(1): Show | 4 | HG00558.hp1 HG00609.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+12200C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486163 | ||||||
| chr21:38486175
|
T | C | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+12188A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486175 | ||||||
| chr21:38486180
|
G | A | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+12183C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486180 | ||||||
| chr21:38486185
|
A | G | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+12178T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486185 | ||||||
| chr21:38486287
|
G | A | 43 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0172others(40): Show | 44 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.18+12076C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486287 | ||||||
| chr21:38486290
|
A | G | 1 | a0001c0001t0027g0346 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.18+12073T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486290 | ||||||
| chr21:38486376
|
T | C | 1 | a0001c0001t0005g0004 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.18+11987A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486376 | ||||||
| chr21:38486804
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.18+11559A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486804 | ||||||
| chr21:38486838
|
C | A | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+11525G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486838 | ||||||
| chr21:38486979
|
A | G | 108 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(105): Show | 109 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.18+11384T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38486979 | ||||||
| chr21:38487120
|
C | CT | 87 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0128others(84): Show | 88 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.18+11242dupA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487120 | ||||||
| chr21:38487120
|
CT | C | 68 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.18+11242delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487120 | ||||||
| chr21:38487120
|
CTT | C | 46 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0172others(43): Show | 47 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.18+11241_18+11242d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487120 | ||||||
| chr21:38487147
|
G | GA | 294 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.18+11215dupT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487147 | ||||||
| chr21:38487147
|
G | GAA | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+11214_18+11215d others(4): Show |
ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487147 | ||||||
| chr21:38487248
|
CA | C | 5 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0357others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+11114delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487248 | ||||||
| chr21:38487267
|
A | G | 62 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(59): Show | 62 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.18+11096T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487267 | ||||||
| chr21:38487285
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+11078G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487285 | ||||||
| chr21:38487546
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG01257.hp2 HG01258.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.18+10817T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487546 | ||||||
| chr21:38487799
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0159a0001c0001t0001g0163others(3): Show | 6 | HG01081.hp2 HG01952.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+10564A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38487799 | ||||||
| chr21:38488036
|
C | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | NA18946.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.18+10327G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488036 | ||||||
| chr21:38488037
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.18+10326G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488037 | ||||||
| chr21:38488153
|
C | G | 1 | a0001c0002t0012g0228 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.18+10210G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488153 | ||||||
| chr21:38488155
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG00673.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.18+10208T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488155 | ||||||
| chr21:38488249
|
G | C | 1 | a0001c0001t0006g0046 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.18+10114C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488249 | ||||||
| chr21:38488284
|
G | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0006t0001g0177 | 3 | HG02602.hp1 HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.18+10079C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488284 | ||||||
| chr21:38488333
|
G | A | 45 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0172others(42): Show | 46 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.18+10030C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488333 | ||||||
| chr21:38488369
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.18+9994T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488369 | ||||||
| chr21:38488385
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.18+9978G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488385 | ||||||
| chr21:38488516
|
AG | A | 5 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0357others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+9846delC | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488516 | ||||||
| chr21:38488716
|
T | G | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+9647A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488716 | ||||||
| chr21:38488764
|
T | G | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+9599A>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488764 | ||||||
| chr21:38488765
|
C | T | 75 | a0001c0001t0001g0061a0001c0001t0001g0156a0001c0001t0001g0158others(72): Show | 75 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.18+9598G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488765 | ||||||
| chr21:38488808
|
C | T | 5 | a0001c0001t0001g0344a0001c0001t0002g0345a0001c0001t0003g0342others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+9555G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488808 | ||||||
| chr21:38488809
|
C | T | 7 | a0001c0001t0001g0127a0001c0001t0002g0121a0001c0001t0002g0122others(4): Show | 7 | HG01106.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+9554G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488809 | ||||||
| chr21:38488812
|
C | T | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+9551G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38488812 | ||||||
| chr21:38489457
|
T | C | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+8906A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489457 | ||||||
| chr21:38489637
|
G | C | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+8726C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489637 | ||||||
| chr21:38489724
|
C | T | 1 | a0001c0001t0007g0009 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.18+8639G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489724 | ||||||
| chr21:38489807
|
T | C | 154 | a0001c0001t0001g0061a0001c0001t0001g0143a0001c0001t0001g0145others(151): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.18+8556A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489807 | ||||||
| chr21:38489880
|
G | T | 153 | a0001c0001t0001g0061a0001c0001t0001g0143a0001c0001t0001g0145others(150): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.18+8483C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489880 | ||||||
| chr21:38489906
|
T | C | 293 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(290): Show | 294 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.18+8457A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489906 | ||||||
| chr21:38489923
|
C | T | 15 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(12): Show | 15 | HG00609.hp2 HG01106.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+8440G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489923 | ||||||
| chr21:38489941
|
C | T | 30 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(27): Show | 30 | HG00597.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.18+8422G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489941 | ||||||
| chr21:38489996
|
C | T | 1 | a0001c0001t0002g0296 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.18+8367G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38489996 | ||||||
| chr21:38490115
|
C | T | 20 | a0001c0001t0001g0306a0001c0001t0001g0309a0001c0001t0001g0311others(17): Show | 20 | HG02080.hp1 NA18940.hp1 NA18942.hp1 others(17): Show |
intron_variant | MODIFIER | c.18+8248G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38490115 | ||||||
| chr21:38490420
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.18+7943T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38490420 | ||||||
| chr21:38490773
|
C | T | 13 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0172others(10): Show | 13 | HG02074.hp1 HG02523.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.18+7590G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38490773 | ||||||
| chr21:38490900
|
C | T | 1 | a0001c0001t0022g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+7463G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38490900 | ||||||
| chr21:38491094
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+7269C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491094 | ||||||
| chr21:38491183
|
C | T | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+7180G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491183 | ||||||
| chr21:38491206
|
TA | T | 128 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(125): Show | 128 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.18+7156delT | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491206 | ||||||
| chr21:38491242
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.18+7121C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491242 | ||||||
| chr21:38491300
|
G | C | 3 | a0001c0001t0001g0143a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG01257.hp2 HG01258.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.18+7063C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491300 | ||||||
| chr21:38491361
|
T | A | 160 | a0001c0001t0001g0061a0001c0001t0001g0143a0001c0001t0001g0145others(157): Show | 160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.18+7002A>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491361 | ||||||
| chr21:38491729
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.18+6634G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491729 | ||||||
| chr21:38491755
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18+6608C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491755 | ||||||
| chr21:38491763
|
C | A | 3 | a0001c0001t0001g0143a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG01257.hp2 HG01258.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.18+6600G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491763 | ||||||
| chr21:38491963
|
CTGCCTAT others(98): Show |
C | 62 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(59): Show | 62 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.18+6295_18+6399del | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491963 | ||||||
| chr21:38491973
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | HG01257.hp2 HG01258.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.18+6390C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38491973 | ||||||
| chr21:38492011
|
C | A | 1 | a0001c0001t0001g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.18+6352G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492011 | ||||||
| chr21:38492012
|
G | A | 104 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(101): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.18+6351C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492012 | ||||||
| chr21:38492028
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.18+6335T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492028 | ||||||
| chr21:38492090
|
A | C | 168 | a0001c0001t0001g0061a0001c0001t0001g0135a0001c0001t0001g0136others(165): Show | 168 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.18+6273T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492090 | ||||||
| chr21:38492180
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.18+6183G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492180 | ||||||
| chr21:38492311
|
G | T | 1 | a0001c0001t0002g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+6052C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492311 | ||||||
| chr21:38492340
|
C | G | 2 | a0001c0001t0006g0049a0001c0001t0016g0048 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.18+6023G>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492340 | ||||||
| chr21:38492477
|
C | A | 1 | a0001c0001t0028g0284 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+5886G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492477 | ||||||
| chr21:38492612
|
C | T | 1 | a0001c0001t0005g0004 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.18+5751G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492612 | ||||||
| chr21:38492660
|
A | G | 111 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(108): Show | 111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.18+5703T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492660 | ||||||
| chr21:38492726
|
C | A | 1 | a0001c0001t0001g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.18+5637G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492726 | ||||||
| chr21:38492803
|
A | G | 294 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(291): Show | 295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.18+5560T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38492803 | ||||||
| chr21:38493100
|
AT | A | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+5262delA | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38493100 | ||||||
| chr21:38493119
|
A | T | 15 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(12): Show | 15 | HG00609.hp2 HG01106.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+5244T>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38493119 | ||||||
| chr21:38493226
|
C | T | 44 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0172others(41): Show | 45 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.18+5137G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38493226 | ||||||
| chr21:38493375
|
C | T | 1 | a0001c0001t0011g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+4988G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38493375 | ||||||
| chr21:38493414
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.18+4949G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38493414 | ||||||
| chr21:38493415
|
G | A | 45 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0172others(42): Show | 46 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.18+4948C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38493415 | ||||||
| chr21:38493931
|
C | T | 58 | a0001c0001t0001g0061a0001c0001t0001g0127a0001c0001t0001g0156others(55): Show | 59 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.18+4432G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38493931 | ||||||
| chr21:38494244
|
G | C | 3 | a0001c0001t0001g0344a0001c0001t0003g0342a0001c0001t0003g0343 | 3 | HG02280.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.18+4119C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38494244 | ||||||
| chr21:38494278
|
G | A | 1 | a0001c0003t0001g0293 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.18+4085C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38494278 | ||||||
| chr21:38494376
|
G | C | 1 | a0001c0002t0012g0294 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.18+3987C>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38494376 | ||||||
| chr21:38494665
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.18+3698C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38494665 | ||||||
| chr21:38494834
|
C | T | 12 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(9): Show | 12 | HG02027.hp1 HG02083.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.18+3529G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38494834 | ||||||
| chr21:38494900
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.18+3463G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38494900 | ||||||
| chr21:38495222
|
C | A | 1 | a0001c0001t0002g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.18+3141G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38495222 | ||||||
| chr21:38495287
|
A | C | 26 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(23): Show | 26 | HG00544.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+3076T>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38495287 | ||||||
| chr21:38495396
|
G | A | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+2967C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38495396 | ||||||
| chr21:38495871
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.18+2492C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38495871 | ||||||
| chr21:38496147
|
C | A | 2 | a0001c0001t0002g0296a0001c0001t0008g0297 | 2 | HG02027.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.18+2216G>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38496147 | ||||||
| chr21:38496326
|
G | A | 50 | a0001c0001t0001g0306a0001c0001t0001g0309a0001c0001t0001g0311others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.18+2037C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38496326 | ||||||
| chr21:38496613
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.18+1750G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38496613 | ||||||
| chr21:38496857
|
A | G | 64 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.18+1506T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38496857 | ||||||
| chr21:38497003
|
T | C | 312 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(309): Show | 313 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.18+1360A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38497003 | ||||||
| chr21:38497214
|
T | C | 2 | a0001c0001t0002g0345a0001c0001t0027g0346 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.18+1149A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38497214 | ||||||
| chr21:38497329
|
T | C | 5 | a0001c0001t0001g0351a0001c0001t0002g0347a0001c0001t0002g0348others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+1034A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38497329 | ||||||
| chr21:38497417
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.18+946T>C | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38497417 | ||||||
| chr21:38497428
|
T | C | 1 | a0001c0001t0004g0055 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.18+935A>G | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38497428 | ||||||
| chr21:38497573
|
G | T | 1 | a0001c0001t0003g0057 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.18+790C>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38497573 | ||||||
| chr21:38497705
|
G | A | 6 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0357others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+658C>T | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38497705 | ||||||
| chr21:38497904
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.18+459G>A | ERG | ENSG00000157554.20 | transcript | ENST00000288319.12 | protein_coding | 1/9 | chr21 | 38497904 |