| geneid | 400746 |
|---|---|
| ensemblid | ENSG00000184454.7 |
| hgncid | 29332 |
| symbol | NCMAP |
| name | non-compact myelin associated protein |
| refseq_nuc | NM_001010980.5 |
| refseq_prot | NP_001010980.1 |
| ensembl_nuc | ENST00000374392.3 |
| ensembl_prot | ENSP00000363513.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 24556087 |
| end | 24609328 |
| strand | + |
| ver | v1.2 |
| region | chr1:24556087-24609328 |
| region5000 | chr1:24551087-24614328 |
| regionname0 | NCMAP_chr1_24556087_24609328 |
| regionname5000 | NCMAP_chr1_24551087_24614328 |
| 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 | 102 | 378 | 72 | 72 | 170 | 18 | 44 | 128 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0002 | 0/0 | 102 | 23 | 21 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0003 | 0/0 | 102 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| 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 | 309 | 378 | 72 | 72 | 170 | 18 | 44 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| c0002 | 0/0 | 309 | 23 | 21 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| c0003 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3672 | 136 | 23 | 32 | 57 | 8 | 15 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0002 | 0/1 | 3673 | 85 | 0 | 17 | 49 | 4 | 14 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0003 | 0/0 | 3672 | 73 | 17 | 14 | 28 | 4 | 10 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0004 | 0/0 | 3650 | 19 | 17 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0005 | 0/0 | 3673 | 18 | 0 | 3 | 15 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0006 | 0/0 | 3673 | 14 | 5 | 3 | 4 | 1 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0007 | 0/0 | 3671 | 11 | 0 | 1 | 9 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0008 | 0/0 | 3673 | 10 | 10 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0009 | 0/0 | 3672 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0010 | 0/0 | 3673 | 3 | 2 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0011 | 0/0 | 3673 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0012 | 0/0 | 3673 | 3 | 1 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0013 | 0/0 | 3651 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0014 | 0/0 | 3674 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0015 | 0/0 | 3673 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0016 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0017 | 0/0 | 3673 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0018 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0019 | 0/0 | 3673 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0020 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0021 | 0/0 | 3673 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0022 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0023 | 0/0 | 3673 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0024 | 0/0 | 3673 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0025 | 0/0 | 3674 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0026 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0027 | 0/0 | 3672 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0028 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0029 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0030 | 0/0 | 3672 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0031 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| t0032 | 0/0 | 3673 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| 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 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| 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 | 309 | 378 | 72 | 72 | 170 | 18 | 44 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0002c0002 | 0/0 | 309 | 23 | 21 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0003c0003 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3980 | 136 | 23 | 32 | 57 | 8 | 15 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0002 | 0/1 | 3981 | 85 | 0 | 17 | 49 | 4 | 14 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0003 | 0/0 | 3980 | 73 | 17 | 14 | 28 | 4 | 10 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0005 | 0/0 | 3981 | 18 | 0 | 3 | 15 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0006 | 0/0 | 3981 | 14 | 5 | 3 | 4 | 1 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0007 | 0/0 | 3979 | 11 | 0 | 1 | 9 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0008 | 0/0 | 3981 | 10 | 10 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0009 | 0/0 | 3980 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0010 | 0/0 | 3981 | 3 | 2 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0011 | 0/0 | 3981 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0012 | 0/0 | 3981 | 3 | 1 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0014 | 0/0 | 3982 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0015 | 0/0 | 3981 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0016 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0017 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0018 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0019 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0020 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0021 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0022 | 0/0 | 4013 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0023 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0024 | 0/0 | 3981 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0025 | 0/0 | 3982 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0026 | 0/0 | 3980 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0028 | 0/0 | 3980 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0029 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0030 | 0/0 | 3980 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0001c0001t0032 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0002c0002t0004 | 0/0 | 3958 | 19 | 17 | 2 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0002c0002t0013 | 0/0 | 3959 | 3 | 3 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0002c0002t0031 | 0/0 | 3958 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| a0003c0003t0027 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | copy fasta | chr1 | 24551087 | 24614328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0001g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0003g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0006g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0007g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0008g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0009g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0011g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0011g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0012g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0012g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0014g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0014g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0016g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0017g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0018g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0019g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0020g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0021g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0022g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0023g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0024g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0025g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0026g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0028g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0029g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0030g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0001c0001t0032g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0004g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0013g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0002c0002t0031g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| a0003c0003t0027g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0352 | EUR | GBR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | GBR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0244 | EUR | GBR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | FIN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0363 | EUR | FIN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0321 | EUR | FIN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | FIN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0375 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0382 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0359 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0378 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01069 | hp2 | a0001 | c0001 | t0012 | g0215 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01071 | hp2 | a0001 | c0001 | t0012 | g0202 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0355 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01099 | hp2 | a0002 | c0002 | t0004 | g0389 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0320 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0272 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0152 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0017 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0278 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0333 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0176 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0371 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01516 | hp1 | a0001 | c0001 | t0026 | g0142 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0354 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0141 | EUR | IBS | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0287 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01884 | hp2 | a0002 | c0002 | t0004 | g0029 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0379 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0395 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0171 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0177 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0365 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02027 | hp1 | a0001 | c0001 | t0019 | g0347 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0399 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0374 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0341 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | CDX | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | CDX | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CDX | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | CDX | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0273 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0400 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0067 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0385 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0023 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0150 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0397 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02630 | hp2 | a0001 | c0001 | t0015 | g0009 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0030 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0369 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0065 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02723 | hp2 | a0002 | c0002 | t0013 | g0146 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02809 | hp1 | a0002 | c0002 | t0004 | g0390 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02818 | hp1 | a0002 | c0002 | t0004 | g0275 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0327 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0366 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02896 | hp2 | a0002 | c0002 | t0004 | g0391 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0393 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0377 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0016 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02976 | hp2 | a0002 | c0002 | t0004 | g0031 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0364 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03041 | hp2 | a0003 | c0003 | t0027 | g0276 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0059 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0290 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0394 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03139 | hp2 | a0002 | c0002 | t0004 | g0057 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0386 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03209 | hp1 | a0001 | c0001 | t0018 | g0013 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03209 | hp2 | a0002 | c0002 | t0013 | g0002 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0008 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0266 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0361 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0380 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0274 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0387 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03486 | hp2 | a0002 | c0002 | t0013 | g0002 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03490 | hp1 | a0001 | c0001 | t0024 | g0101 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0358 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0357 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0381 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0148 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0060 | AFR | GWD | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0151 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0074 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | BEB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04199 | hp1 | a0001 | c0001 | t0030 | g0003 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04204 | hp1 | a0001 | c0001 | t0028 | g0159 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0360 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | STU | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0372 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18522 | hp2 | a0002 | c0002 | t0031 | g0024 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | CHB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | CHB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18906 | hp1 | a0001 | c0001 | t0032 | g0317 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0306 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18948 | hp1 | a0001 | c0001 | t0021 | g0175 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0370 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0304 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18961 | hp2 | a0001 | c0001 | t0020 | g0268 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18963 | hp2 | a0001 | c0001 | t0025 | g0087 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0373 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18967 | hp1 | a0001 | c0001 | t0010 | g0207 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0297 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18972 | hp2 | a0001 | c0001 | t0029 | g0362 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0368 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18984 | hp2 | a0001 | c0001 | t0007 | g0307 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18992 | hp2 | a0001 | c0001 | t0023 | g0071 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0280 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19004 | hp1 | a0001 | c0001 | t0022 | g0088 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0303 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0388 | AFR | LWK | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19057 | hp2 | a0001 | c0001 | t0007 | g0079 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0383 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0315 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0316 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19240 | hp1 | a0002 | c0002 | t0004 | g0201 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0091 | EUR | TSI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | TSI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0331 | EUR | TSI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0334 | SAS | GIH | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0154 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0376 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02486 | hp1 | a0001 | c0001 | t0014 | g0398 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0396 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0033 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | ACB | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0392 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG03471 | hp2 | a0002 | c0002 | t0004 | g0025 | AFR | MSL | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG06807 | hp1 | a0002 | c0002 | t0004 | g0004 | AFR | USA | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | USA | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA20300 | hp2 | a0002 | c0002 | t0004 | g0006 | AFR | USA | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | LWK | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0135 | REF | REF | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0236 | REF | REF | NCMAP_chr1_24551087_24614328 | NCMAP | chr1 | 24551087 | 24614328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:24605732
|
G | C | 1 | a0002 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
missense_variant | MODERATE | c.294G>C | p.Gln98His | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 384/3980 | 294/309 | 98/102 | chr1 | 24605732 | ||
| chr1:24605740
|
C | T | 1 | a0003 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.302C>T | p.Thr101Met | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 392/3980 | 302/309 | 101/102 | chr1 | 24605740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:24605741
|
G | A | 1 | a0002c0002 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
synonymous_variant | LOW | c.303G>A | p.Thr101Thr | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 393/3980 | 303/309 | 101/102 | chr1 | 24605741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:24605756
|
C | T | 1 | a0001c0001t0032 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 9 | chr1 | 24605756 | |||||
| chr1:24605760
|
C | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*13C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 13 | chr1 | 24605760 | |||||
| chr1:24605834
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*87T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 87 | chr1 | 24605834 | |||||
| chr1:24605872
|
C | T | 1 | a0001c0001t0030 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 125 | chr1 | 24605872 | |||||
| chr1:24605946
|
C | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*199C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 199 | chr1 | 24605946 | |||||
| chr1:24605953
|
C | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 206 | chr1 | 24605953 | |||||
| chr1:24606019
|
A | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*272A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 272 | chr1 | 24606019 | |||||
| chr1:24606040
|
A | G | 1 | a0001c0001t0032 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*293A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 293 | chr1 | 24606040 | |||||
| chr1:24606054
|
CAGAT | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*311_*314delTAGA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 311 | INFO_REALIGN_3_PRIME | chr1 | 24606054 | ||||
| chr1:24606132
|
A | C | 1 | a0001c0001t0029 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 385 | chr1 | 24606132 | |||||
| chr1:24606157
|
T | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*410T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 410 | chr1 | 24606157 | |||||
| chr1:24606167
|
A | G | 1 | a0001c0001t0028 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 420 | chr1 | 24606167 | |||||
| chr1:24606219
|
T | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*472T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 472 | chr1 | 24606219 | |||||
| chr1:24606230
|
C | T | 4 | a0002c0002t0004a0002c0002t0013a0002c0002t0031others(1): Show | 24 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 483 | chr1 | 24606230 | |||||
| chr1:24606242
|
A | G | 14 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(11): Show | 142 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*495A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 495 | chr1 | 24606242 | |||||
| chr1:24606343
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*596T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 596 | chr1 | 24606343 | |||||
| chr1:24606451
|
T | C | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(18): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*704T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 704 | chr1 | 24606451 | |||||
| chr1:24606491
|
C | T | 2 | a0001c0001t0006a0001c0001t0026 | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*744C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 744 | chr1 | 24606491 | |||||
| chr1:24606507
|
G | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 760 | chr1 | 24606507 | |||||
| chr1:24606517
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*770T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 770 | chr1 | 24606517 | |||||
| chr1:24606546
|
A | AC | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*800dupC | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 801 | INFO_REALIGN_3_PRIME | chr1 | 24606546 | ||||
| chr1:24606548
|
G | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*801G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 801 | chr1 | 24606548 | |||||
| chr1:24606565
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*818T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 818 | chr1 | 24606565 | |||||
| chr1:24606585
|
G | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*838G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 838 | chr1 | 24606585 | |||||
| chr1:24606619
|
A | G | 1 | a0003c0003t0027 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 872 | chr1 | 24606619 | |||||
| chr1:24606621
|
G | A | 1 | a0001c0001t0020 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*874G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 874 | chr1 | 24606621 | |||||
| chr1:24606703
|
C | T | 7 | a0001c0001t0002a0001c0001t0005a0001c0001t0021others(4): Show | 108 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*956C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 956 | chr1 | 24606703 | |||||
| chr1:24606859
|
G | C | 1 | a0001c0001t0021 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1112G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1112 | chr1 | 24606859 | |||||
| chr1:24606881
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1134T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1134 | chr1 | 24606881 | |||||
| chr1:24606948
|
T | G | 2 | a0001c0001t0006a0001c0001t0026 | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1201T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1201 | chr1 | 24606948 | |||||
| chr1:24606984
|
CTTTTTTC others(9): Show |
C | 1 | a0002c0002t0013 | 3 | HG02723.hp2 HG03209.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244_*1259delCTTT others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1244 | INFO_REALIGN_3_PRIME | chr1 | 24606984 | ||||
| chr1:24606984
|
CTTTTTTC others(10): Show |
C | 2 | a0002c0002t0004a0002c0002t0031 | 20 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1244_*1260delCTTT others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1244 | INFO_REALIGN_3_PRIME | chr1 | 24606984 | ||||
| chr1:24606996
|
C | CT | 10 | a0001c0001t0006a0001c0001t0008a0001c0001t0010others(7): Show | 40 | HG00558.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1265dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1266 | INFO_REALIGN_3_PRIME | chr1 | 24606996 | ||||
| chr1:24606996
|
CT | C | 2 | a0001c0001t0007a0001c0001t0016 | 12 | HG01168.hp1 HG02145.hp2 HG03239.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1265delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1265 | INFO_REALIGN_3_PRIME | chr1 | 24606996 | ||||
| chr1:24607069
|
G | A | 5 | a0001c0001t0014a0001c0001t0017a0002c0002t0004others(2): Show | 26 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1322G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1322 | chr1 | 24607069 | |||||
| chr1:24607162
|
T | A | 1 | a0001c0001t0011 | 3 | HG01891.hp1 HG02257.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1415T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1415 | chr1 | 24607162 | |||||
| chr1:24607193
|
G | A | 1 | a0003c0003t0027 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1446G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1446 | chr1 | 24607193 | |||||
| chr1:24607221
|
G | A | 1 | a0001c0001t0018 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1474G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1474 | chr1 | 24607221 | |||||
| chr1:24607266
|
G | A | 11 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(8): Show | 126 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1519G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1519 | chr1 | 24607266 | |||||
| chr1:24607267
|
C | T | 1 | a0001c0001t0005 | 18 | HG00597.hp2 HG01358.hp1 HG01928.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1520C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1520 | chr1 | 24607267 | |||||
| chr1:24607388
|
CAT | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1644_*1645delAT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1644 | INFO_REALIGN_3_PRIME | chr1 | 24607388 | ||||
| chr1:24607438
|
C | CAAAGAAC others(26): Show |
1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1691_*1692insAAAG others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1692 | chr1 | 24607438 | |||||
| chr1:24607440
|
C | T | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1693 | chr1 | 24607440 | |||||
| chr1:24607441
|
T | G | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1694T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1694 | chr1 | 24607441 | |||||
| chr1:24607446
|
A | T | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1699 | chr1 | 24607446 | |||||
| chr1:24607458
|
T | G | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1711T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1711 | chr1 | 24607458 | |||||
| chr1:24607465
|
G | C | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1718 | chr1 | 24607465 | |||||
| chr1:24607477
|
G | T | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1730G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1730 | chr1 | 24607477 | |||||
| chr1:24607484
|
G | T | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1737G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1737 | chr1 | 24607484 | |||||
| chr1:24607486
|
T | TA | 8 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(5): Show | 110 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1741dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1742 | INFO_REALIGN_3_PRIME | chr1 | 24607486 | ||||
| chr1:24607489
|
T | G | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1742T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1742 | chr1 | 24607489 | |||||
| chr1:24607500
|
T | C | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1753T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1753 | chr1 | 24607500 | |||||
| chr1:24607501
|
C | T | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1754C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1754 | chr1 | 24607501 | |||||
| chr1:24607504
|
T | C | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1757T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1757 | chr1 | 24607504 | |||||
| chr1:24607505
|
T | A | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1758T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1758 | chr1 | 24607505 | |||||
| chr1:24607507
|
A | T | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1760A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1760 | chr1 | 24607507 | |||||
| chr1:24607508
|
A | T | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1761A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1761 | chr1 | 24607508 | |||||
| chr1:24607517
|
C | A | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1770 | chr1 | 24607517 | |||||
| chr1:24607522
|
T | C | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1775 | chr1 | 24607522 | |||||
| chr1:24607524
|
T | A | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1777T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1777 | chr1 | 24607524 | |||||
| chr1:24607525
|
G | T | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1778 | chr1 | 24607525 | |||||
| chr1:24607542
|
T | G | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1795T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1795 | chr1 | 24607542 | |||||
| chr1:24607584
|
G | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1837G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1837 | chr1 | 24607584 | |||||
| chr1:24607594
|
G | A | 2 | a0001c0001t0006a0001c0001t0026 | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1847G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1847 | chr1 | 24607594 | |||||
| chr1:24607633
|
G | A | 1 | a0001c0001t0022 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1886G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1886 | chr1 | 24607633 | |||||
| chr1:24607636
|
A | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1889A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1889 | chr1 | 24607636 | |||||
| chr1:24607722
|
G | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1975G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1975 | chr1 | 24607722 | |||||
| chr1:24607732
|
G | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1985G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 1985 | chr1 | 24607732 | |||||
| chr1:24607753
|
A | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2006A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2006 | chr1 | 24607753 | |||||
| chr1:24607775
|
A | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2028A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2028 | chr1 | 24607775 | |||||
| chr1:24607900
|
G | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2153G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2153 | chr1 | 24607900 | |||||
| chr1:24607920
|
T | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2173T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2173 | chr1 | 24607920 | |||||
| chr1:24607944
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2197T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2197 | chr1 | 24607944 | |||||
| chr1:24607972
|
T | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2225T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2225 | chr1 | 24607972 | |||||
| chr1:24607974
|
G | A | 1 | a0002c0002t0013 | 3 | HG02723.hp2 HG03209.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2227G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2227 | chr1 | 24607974 | |||||
| chr1:24608127
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2380T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2380 | chr1 | 24608127 | |||||
| chr1:24608145
|
T | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2398T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2398 | chr1 | 24608145 | |||||
| chr1:24608161
|
G | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2414G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2414 | chr1 | 24608161 | |||||
| chr1:24608183
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2436T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2436 | chr1 | 24608183 | |||||
| chr1:24608218
|
G | C | 1 | a0002c0002t0031 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2471G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2471 | chr1 | 24608218 | |||||
| chr1:24608271
|
C | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2524C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2524 | chr1 | 24608271 | |||||
| chr1:24608280
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2533T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2533 | chr1 | 24608280 | |||||
| chr1:24608281
|
G | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2534G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2534 | chr1 | 24608281 | |||||
| chr1:24608286
|
A | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2539A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2539 | chr1 | 24608286 | |||||
| chr1:24608353
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2606T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2606 | chr1 | 24608353 | |||||
| chr1:24608380
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2633T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2633 | chr1 | 24608380 | |||||
| chr1:24608381
|
G | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2634G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2634 | chr1 | 24608381 | |||||
| chr1:24608531
|
C | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2784C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2784 | chr1 | 24608531 | |||||
| chr1:24608590
|
T | C | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2843T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2843 | chr1 | 24608590 | |||||
| chr1:24608606
|
G | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2859G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2859 | chr1 | 24608606 | |||||
| chr1:24608626
|
G | A | 1 | a0001c0001t0009 | 3 | HG02055.hp2 HG02280.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2879G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2879 | chr1 | 24608626 | |||||
| chr1:24608635
|
C | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2888C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2888 | chr1 | 24608635 | |||||
| chr1:24608680
|
G | A | 1 | a0001c0001t0023 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2933G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2933 | chr1 | 24608680 | |||||
| chr1:24608713
|
C | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2966C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 2966 | chr1 | 24608713 | |||||
| chr1:24608762
|
A | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3015A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3015 | chr1 | 24608762 | |||||
| chr1:24608850
|
C | T | 1 | a0001c0001t0032 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3103C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3103 | chr1 | 24608850 | |||||
| chr1:24608939
|
G | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3192G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3192 | chr1 | 24608939 | |||||
| chr1:24608950
|
A | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3203A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3203 | chr1 | 24608950 | |||||
| chr1:24608953
|
G | C | 6 | a0001c0001t0003a0001c0001t0016a0001c0001t0018others(3): Show | 78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3206G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3206 | chr1 | 24608953 | |||||
| chr1:24609035
|
T | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3288T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3288 | chr1 | 24609035 | |||||
| chr1:24609075
|
A | T | 1 | a0001c0001t0024 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3328A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3328 | chr1 | 24609075 | |||||
| chr1:24609079
|
G | A | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3332G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3332 | chr1 | 24609079 | |||||
| chr1:24609157
|
C | T | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3410C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3410 | chr1 | 24609157 | |||||
| chr1:24609187
|
A | G | 3 | a0002c0002t0004a0002c0002t0013a0002c0002t0031 | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3440A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3440 | chr1 | 24609187 | |||||
| chr1:24609232
|
C | T | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3485C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3485 | chr1 | 24609232 | |||||
| chr1:24609259
|
G | A | 1 | a0001c0001t0012 | 3 | HG01069.hp2 HG01071.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3512G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4/4 | 3512 | chr1 | 24609259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:24556177
|
G | A | 1 | a0001c0001t0030g0003 | 1 | HG04199.hp1 | splice_region_variant&intron_variant | LOW | c.-8+8G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556177 | ||||||
| chr1:24556263
|
C | T | 14 | a0001c0001t0001g0400a0001c0001t0003g0387a0001c0001t0003g0388others(11): Show | 14 | HG01099.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8+94C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556263 | ||||||
| chr1:24556285
|
G | A | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+116G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556285 | ||||||
| chr1:24556304
|
C | T | 1 | a0001c0001t0006g0386 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-8+135C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556304 | ||||||
| chr1:24556314
|
A | G | 69 | a0001c0001t0001g0318a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-8+145A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556314 | ||||||
| chr1:24556399
|
A | G | 84 | a0001c0001t0001g0318a0001c0001t0001g0322a0001c0001t0001g0323others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+230A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556399 | ||||||
| chr1:24556406
|
C | T | 70 | a0001c0001t0001g0318a0001c0001t0001g0322a0001c0001t0001g0323others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-8+237C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556406 | ||||||
| chr1:24556436
|
C | T | 45 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(42): Show | 45 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+267C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556436 | ||||||
| chr1:24556448
|
A | C | 70 | a0001c0001t0001g0318a0001c0001t0001g0322a0001c0001t0001g0323others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-8+279A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556448 | ||||||
| chr1:24556473
|
T | A | 1 | a0001c0001t0008g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8+304T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556473 | ||||||
| chr1:24556489
|
C | T | 1 | a0001c0001t0007g0272 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-8+320C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556489 | ||||||
| chr1:24556661
|
T | C | 152 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(149): Show | 154 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.-8+492T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556661 | ||||||
| chr1:24556668
|
A | G | 152 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(149): Show | 154 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.-8+499A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556668 | ||||||
| chr1:24556688
|
C | A | 152 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(149): Show | 154 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.-8+519C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556688 | ||||||
| chr1:24556705
|
G | A | 149 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-8+536G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556705 | ||||||
| chr1:24556743
|
C | T | 198 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-8+574C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556743 | ||||||
| chr1:24556790
|
C | T | 3 | a0001c0001t0006g0151a0001c0001t0006g0152a0001c0001t0006g0153 | 3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8+621C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556790 | ||||||
| chr1:24556809
|
G | A | 2 | a0001c0001t0015g0008a0001c0001t0015g0009 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-8+640G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556809 | ||||||
| chr1:24556993
|
C | T | 1 | a0001c0001t0006g0316 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-8+824C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24556993 | ||||||
| chr1:24557060
|
G | C | 264 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-8+891G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557060 | ||||||
| chr1:24557151
|
G | A | 26 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(23): Show | 26 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8+982G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557151 | ||||||
| chr1:24557374
|
GGTGCATG others(9): Show |
G | 1 | a0001c0001t0002g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-8+1218_-8+1233del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24557374 | |||||
| chr1:24557413
|
TTGTGTGC others(3): Show |
T | 82 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0158others(79): Show | 82 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-8+1257_-8+1266del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24557413 | |||||
| chr1:24557446
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0382 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+1295_-8+1304del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24557446 | |||||
| chr1:24557465
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-8+1296G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557465 | ||||||
| chr1:24557578
|
G | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0011 | 2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8+1409G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557578 | ||||||
| chr1:24557599
|
A | G | 1 | a0002c0002t0004g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8+1430A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557599 | ||||||
| chr1:24557626
|
A | C | 1 | a0001c0001t0003g0381 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-8+1457A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557626 | ||||||
| chr1:24557726
|
C | G | 1 | a0001c0001t0003g0147 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-8+1557C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557726 | ||||||
| chr1:24557823
|
C | A | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+1654C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557823 | ||||||
| chr1:24557830
|
C | T | 2 | a0001c0001t0011g0379a0001c0001t0011g0380 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+1661C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557830 | ||||||
| chr1:24557831
|
G | C | 3 | a0001c0001t0003g0319a0001c0001t0003g0320a0001c0001t0003g0321 | 3 | HG00323.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-8+1662G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557831 | ||||||
| chr1:24557834
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+1665G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557834 | ||||||
| chr1:24557836
|
G | A | 176 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-8+1667G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557836 | ||||||
| chr1:24557839
|
C | A | 3 | a0001c0001t0006g0151a0001c0001t0006g0152a0001c0001t0006g0153 | 3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8+1670C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557839 | ||||||
| chr1:24557893
|
GA | G | 6 | a0001c0001t0001g0400a0001c0001t0008g0396a0001c0001t0014g0397others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+1726delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24557893 | |||||
| chr1:24557913
|
C | T | 9 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+1744C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557913 | ||||||
| chr1:24557969
|
A | G | 191 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(188): Show | 193 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-8+1800A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557969 | ||||||
| chr1:24557988
|
G | A | 4 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0002g0218others(1): Show | 4 | NA18950.hp1 NA18952.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+1819G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24557988 | ||||||
| chr1:24558052
|
C | T | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+1883C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558052 | ||||||
| chr1:24558168
|
C | T | 9 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+1999C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558168 | ||||||
| chr1:24558225
|
T | C | 2 | a0001c0001t0011g0379a0001c0001t0011g0380 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+2056T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558225 | ||||||
| chr1:24558369
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-8+2200T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558369 | ||||||
| chr1:24558432
|
G | C | 1 | a0001c0001t0012g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8+2263G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558432 | ||||||
| chr1:24558625
|
A | G | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+2456A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558625 | ||||||
| chr1:24558638
|
T | C | 1 | a0001c0001t0003g0387 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+2469T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558638 | ||||||
| chr1:24558703
|
C | T | 13 | a0001c0001t0001g0144a0001c0001t0001g0322a0001c0001t0001g0376others(10): Show | 14 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8+2534C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558703 | ||||||
| chr1:24558766
|
T | G | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+2597T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558766 | ||||||
| chr1:24558771
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-8+2602T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558771 | ||||||
| chr1:24558965
|
T | TA | 15 | a0001c0001t0001g0156a0001c0001t0003g0010a0001c0001t0003g0011others(12): Show | 16 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+2806dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24558965 | |||||
| chr1:24558981
|
T | C | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(25): Show | 28 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8+2812T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24558981 | ||||||
| chr1:24559245
|
A | C | 4 | a0001c0001t0001g0400a0001c0001t0014g0397a0001c0001t0014g0398others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+3076A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559245 | ||||||
| chr1:24559360
|
C | A | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3191C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559360 | ||||||
| chr1:24559361
|
C | A | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3192C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559361 | ||||||
| chr1:24559498
|
A | G | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3329A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559498 | ||||||
| chr1:24559566
|
C | T | 1 | a0001c0001t0003g0321 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-8+3397C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559566 | ||||||
| chr1:24559637
|
C | T | 22 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(19): Show | 22 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8+3468C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559637 | ||||||
| chr1:24559645
|
G | A | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3476G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559645 | ||||||
| chr1:24559669
|
T | C | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3500T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559669 | ||||||
| chr1:24559691
|
G | A | 4 | a0001c0001t0001g0400a0001c0001t0014g0397a0001c0001t0014g0398others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+3522G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559691 | ||||||
| chr1:24559747
|
C | A | 1 | a0001c0001t0001g0382 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+3578C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559747 | ||||||
| chr1:24559889
|
C | G | 1 | a0001c0001t0002g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-8+3720C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559889 | ||||||
| chr1:24559936
|
T | C | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3767T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24559936 | ||||||
| chr1:24560002
|
A | G | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+3833A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560002 | ||||||
| chr1:24560018
|
G | A | 2 | a0001c0001t0008g0396a0002c0002t0004g0395 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-8+3849G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560018 | ||||||
| chr1:24560086
|
G | A | 131 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-8+3917G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560086 | ||||||
| chr1:24560158
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-8+3989C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560158 | ||||||
| chr1:24560160
|
C | CA | 101 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(98): Show | 101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-8+4016dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | |||||
| chr1:24560160
|
C | CAA | 9 | a0001c0001t0001g0158a0001c0001t0001g0221a0001c0001t0002g0021others(6): Show | 9 | HG01099.hp2 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+4015_-8+4016dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | |||||
| chr1:24560160
|
CA | C | 48 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0140others(45): Show | 49 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.-8+4016delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | |||||
| chr1:24560160
|
CAAAA | C | 23 | a0001c0001t0001g0144a0001c0001t0001g0322a0001c0001t0001g0376others(20): Show | 24 | HG00639.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8+4013_-8+4016del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | |||||
| chr1:24560160
|
CAAAAA | C | 55 | a0001c0001t0001g0318a0001c0001t0001g0331a0001c0001t0001g0332others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8+4012_-8+4016del others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560160 | |||||
| chr1:24560222
|
G | T | 1 | a0001c0001t0030g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8+4053G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560222 | ||||||
| chr1:24560288
|
G | T | 2 | a0001c0001t0003g0373a0001c0001t0003g0374 | 2 | HG02080.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-8+4119G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560288 | ||||||
| chr1:24560293
|
A | G | 1 | a0001c0001t0003g0372 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8+4124A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560293 | ||||||
| chr1:24560327
|
G | A | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+4158G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560327 | ||||||
| chr1:24560371
|
T | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | NA18954.hp2 NA18960.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-8+4202T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560371 | ||||||
| chr1:24560627
|
C | G | 4 | a0001c0001t0008g0001a0001c0001t0008g0018a0001c0001t0008g0019others(1): Show | 5 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+4458C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560627 | ||||||
| chr1:24560637
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG00323.hp2 HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-8+4468G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560637 | ||||||
| chr1:24560747
|
GA | G | 13 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(10): Show | 14 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+4590delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560747 | |||||
| chr1:24560772
|
CTT | C | 10 | a0001c0001t0001g0400a0001c0001t0003g0392a0001c0001t0003g0394others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+4606_-8+4607del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24560772 | |||||
| chr1:24560966
|
C | T | 131 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-8+4797C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24560966 | ||||||
| chr1:24561056
|
G | A | 82 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(79): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-8+4887G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561056 | ||||||
| chr1:24561108
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-8+4939G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561108 | ||||||
| chr1:24561130
|
C | T | 48 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0227others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.-8+4961C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561130 | ||||||
| chr1:24561178
|
C | CA | 188 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+5029dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561178 | |||||
| chr1:24561178
|
C | CAA | 62 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0051others(59): Show | 62 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-8+5028_-8+5029dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561178 | |||||
| chr1:24561178
|
C | CAAA | 63 | a0001c0001t0001g0158a0001c0001t0001g0223a0001c0001t0001g0230others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-8+5027_-8+5029dup others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561178 | |||||
| chr1:24561178
|
C | CAAAA | 20 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0331others(17): Show | 22 | HG01109.hp2 HG01255.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8+5026_-8+5029dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561178 | |||||
| chr1:24561210
|
G | A | 37 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(34): Show | 37 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-8+5041G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561210 | ||||||
| chr1:24561257
|
G | T | 4 | a0001c0001t0001g0144a0001c0001t0003g0145a0002c0002t0013g0002others(1): Show | 5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+5088G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561257 | ||||||
| chr1:24561302
|
G | A | 3 | a0001c0001t0006g0151a0001c0001t0006g0152a0001c0001t0006g0153 | 3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8+5133G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561302 | ||||||
| chr1:24561429
|
G | A | 281 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-8+5260G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561429 | ||||||
| chr1:24561475
|
A | C | 318 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(315): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.-8+5306A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561475 | ||||||
| chr1:24561487
|
A | C | 281 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-8+5318A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561487 | ||||||
| chr1:24561529
|
C | T | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+5360C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561529 | ||||||
| chr1:24561586
|
T | C | 3 | a0001c0001t0006g0151a0001c0001t0006g0152a0001c0001t0006g0153 | 3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-8+5417T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561586 | ||||||
| chr1:24561633
|
G | A | 13 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(10): Show | 14 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+5464G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561633 | ||||||
| chr1:24561637
|
G | A | 2 | a0001c0001t0015g0008a0001c0001t0015g0009 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-8+5468G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561637 | ||||||
| chr1:24561638
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0050 | 2 | HG00438.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-8+5469C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561638 | ||||||
| chr1:24561769
|
G | C | 1 | a0001c0001t0003g0334 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-8+5600G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561769 | ||||||
| chr1:24561872
|
C | T | 281 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-8+5703C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24561872 | ||||||
| chr1:24561910
|
CA | C | 53 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(50): Show | 54 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-8+5756delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561910 | |||||
| chr1:24561910
|
CAA | C | 279 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(276): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.-8+5755_-8+5756del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24561910 | |||||
| chr1:24562094
|
C | T | 281 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-8+5925C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562094 | ||||||
| chr1:24562260
|
G | C | 281 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-8+6091G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562260 | ||||||
| chr1:24562299
|
C | G | 1 | a0001c0001t0002g0296 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-8+6130C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562299 | ||||||
| chr1:24562482
|
G | C | 145 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.-8+6313G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562482 | ||||||
| chr1:24562525
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-8+6356A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562525 | ||||||
| chr1:24562566
|
C | T | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8+6397C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562566 | ||||||
| chr1:24562568
|
C | T | 9 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+6399C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562568 | ||||||
| chr1:24562685
|
G | T | 1 | a0001c0001t0030g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8+6516G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562685 | ||||||
| chr1:24562775
|
C | T | 13 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(10): Show | 14 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+6606C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562775 | ||||||
| chr1:24562866
|
A | G | 63 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161others(60): Show | 63 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-8+6697A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562866 | ||||||
| chr1:24562922
|
C | CCT | 7 | a0001c0001t0001g0048a0001c0001t0002g0129a0001c0001t0002g0130others(4): Show | 7 | HG00544.hp1 HG00621.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+6755_-8+6756dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24562922 | |||||
| chr1:24562959
|
A | T | 131 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0001g0156others(128): Show | 131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-8+6790A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24562959 | ||||||
| chr1:24562975
|
T | TG | 38 | a0001c0001t0001g0127a0001c0001t0001g0281a0001c0001t0001g0282others(35): Show | 38 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-8+6814dupG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24562975 | |||||
| chr1:24563083
|
C | T | 4 | a0001c0001t0003g0392a0001c0001t0003g0394a0002c0002t0004g0391others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+6914C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563083 | ||||||
| chr1:24563253
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-8+7084G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563253 | ||||||
| chr1:24563258
|
GCGCCTGT others(82): Show |
G | 1 | a0001c0001t0001g0382 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+7091_-8+7179del others(89): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563258 | |||||
| chr1:24563333
|
C | A | 44 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(41): Show | 45 | HG00558.hp1 HG00639.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+7164C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563333 | ||||||
| chr1:24563381
|
C | T | 45 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(42): Show | 46 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8+7212C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563381 | ||||||
| chr1:24563382
|
G | A | 1 | a0001c0001t0001g0384 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-8+7213G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563382 | ||||||
| chr1:24563393
|
T | G | 45 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(42): Show | 46 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8+7224T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563393 | ||||||
| chr1:24563398
|
G | A | 5 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(2): Show | 5 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+7229G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563398 | ||||||
| chr1:24563453
|
C | T | 1 | a0001c0001t0001g0367 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-8+7284C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563453 | ||||||
| chr1:24563470
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0003g0145a0002c0002t0013g0002others(1): Show | 5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+7301C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563470 | ||||||
| chr1:24563478
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0003g0145a0002c0002t0013g0002others(1): Show | 5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+7309C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563478 | ||||||
| chr1:24563503
|
C | A | 147 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(144): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.-8+7334C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563503 | ||||||
| chr1:24563520
|
C | A | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+7351C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563520 | ||||||
| chr1:24563534
|
C | CA | 137 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0048others(134): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-8+7383dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563534 | |||||
| chr1:24563534
|
CA | C | 11 | a0001c0001t0001g0214a0001c0001t0001g0269a0001c0001t0001g0400others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+7383delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563534 | |||||
| chr1:24563534
|
CAA | C | 76 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0322others(73): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.-8+7382_-8+7383del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563534 | |||||
| chr1:24563534
|
CAAA | C | 28 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(25): Show | 28 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8+7381_-8+7383del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24563534 | |||||
| chr1:24563553
|
G | A | 1 | a0001c0001t0007g0180 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-8+7384G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563553 | ||||||
| chr1:24563554
|
A | G | 1 | a0001c0001t0007g0180 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-8+7385A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563554 | ||||||
| chr1:24563559
|
A | G | 2 | a0001c0001t0011g0379a0001c0001t0011g0380 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+7390A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563559 | ||||||
| chr1:24563944
|
A | G | 2 | a0001c0001t0001g0313a0001c0001t0005g0312 | 2 | NA18971.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-8+7775A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24563944 | ||||||
| chr1:24564006
|
C | A | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+7837C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564006 | ||||||
| chr1:24564068
|
T | C | 31 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(28): Show | 31 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8+7899T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564068 | ||||||
| chr1:24564367
|
C | G | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+8198C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564367 | ||||||
| chr1:24564367
|
C | T | 11 | a0001c0001t0001g0156a0001c0001t0001g0203a0001c0001t0001g0204others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+8198C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564367 | ||||||
| chr1:24564392
|
T | C | 192 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8+8223T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564392 | ||||||
| chr1:24564438
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-8+8269G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564438 | ||||||
| chr1:24564470
|
C | T | 2 | a0001c0001t0003g0387a0001c0001t0003g0388 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-8+8301C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564470 | ||||||
| chr1:24564494
|
A | G | 40 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(37): Show | 40 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-8+8325A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564494 | ||||||
| chr1:24564513
|
C | CA | 39 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0056others(36): Show | 40 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-8+8363dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | |||||
| chr1:24564513
|
C | CAA | 20 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0061others(17): Show | 20 | HG01099.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8+8362_-8+8363dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | |||||
| chr1:24564513
|
C | CAAA | 52 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.-8+8361_-8+8363dup others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | |||||
| chr1:24564513
|
C | CAAAA | 32 | a0001c0001t0001g0037a0001c0001t0001g0078a0001c0001t0001g0083others(29): Show | 32 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-8+8360_-8+8363dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | |||||
| chr1:24564513
|
C | CAAAAA | 11 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0047others(8): Show | 11 | HG00738.hp2 HG01123.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+8359_-8+8363dup others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | |||||
| chr1:24564513
|
CA | C | 77 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0158others(74): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-8+8363delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564513 | |||||
| chr1:24564517
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0002g0026a0001c0001t0005g0046 | 2 | NA18939.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-8+8358_-8+8373del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564517 | |||||
| chr1:24564527
|
AAAAAAC | A | 10 | a0001c0001t0002g0279a0001c0001t0002g0291a0001c0001t0002g0292others(7): Show | 10 | HG01167.hp2 HG01192.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+8364_-8+8369del others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564527 | |||||
| chr1:24564528
|
AAAAAC | A | 29 | a0001c0001t0001g0144a0001c0001t0001g0285a0001c0001t0001g0286others(26): Show | 30 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8+8364_-8+8368del others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564528 | |||||
| chr1:24564529
|
AAAAC | A | 9 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(6): Show | 9 | HG01071.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+8364_-8+8367del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24564529 | |||||
| chr1:24564532
|
AC | A | 45 | a0001c0001t0001g0318a0001c0001t0001g0324a0001c0001t0001g0331others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+8364delC | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564532 | ||||||
| chr1:24564533
|
C | A | 164 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(161): Show | 165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.-8+8364C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564533 | ||||||
| chr1:24564623
|
C | A | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+8454C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564623 | ||||||
| chr1:24564670
|
A | G | 192 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8+8501A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564670 | ||||||
| chr1:24564717
|
G | C | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+8548G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564717 | ||||||
| chr1:24564730
|
A | G | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+8561A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564730 | ||||||
| chr1:24564849
|
C | T | 60 | a0001c0001t0001g0318a0001c0001t0001g0323a0001c0001t0001g0324others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-8+8680C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24564849 | ||||||
| chr1:24565055
|
A | T | 6 | a0001c0001t0001g0400a0001c0001t0008g0396a0001c0001t0014g0397others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+8886A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565055 | ||||||
| chr1:24565144
|
C | CT | 69 | a0001c0001t0001g0227a0001c0001t0001g0318a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-8+8990dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565144 | |||||
| chr1:24565144
|
C | T | 1 | a0001c0001t0003g0325 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-8+8975C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565144 | ||||||
| chr1:24565144
|
CT | C | 52 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0001g0055others(49): Show | 53 | HG00408.hp2 HG00673.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8+8990delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565144 | |||||
| chr1:24565144
|
CTT | C | 106 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0048others(103): Show | 107 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-8+8989_-8+8990del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565144 | |||||
| chr1:24565224
|
T | A | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9055T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565224 | ||||||
| chr1:24565284
|
TGACAGGG others(16): Show |
T | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9120_-8+9142del others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565284 | |||||
| chr1:24565410
|
C | CA | 192 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.-8+9241_-8+9242ins others(1): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565410 | ||||||
| chr1:24565572
|
T | TTG | 51 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0160others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-8+9445_-8+9446dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
T | TTGTG | 49 | a0001c0001t0001g0128a0001c0001t0001g0183a0001c0001t0001g0184others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.-8+9443_-8+9446dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
T | TTGTGTG | 15 | a0001c0001t0001g0222a0001c0001t0001g0237a0001c0001t0001g0250others(12): Show | 15 | HG00738.hp1 HG01192.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8+9441_-8+9446dup others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0230a0001c0001t0001g0400a0001c0001t0002g0249others(6): Show | 9 | HG00735.hp2 HG00741.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+9439_-8+9446dup others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0251 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8+9437_-8+9446dup others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
T | TTGTGTGT others(5): Show |
1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-8+9435_-8+9446dup others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
T | TTGTGTGT others(7): Show |
1 | a0002c0002t0013g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8+9433_-8+9446dup others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0144a0001c0001t0003g0145 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8+9431_-8+9446dup others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
T | TTGTGTGT others(11): Show |
1 | a0002c0002t0013g0002 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-8+9429_-8+9446dup others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTG | T | 4 | a0001c0001t0001g0311a0001c0001t0003g0325a0001c0001t0003g0335others(1): Show | 4 | HG02486.hp2 NA18964.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+9445_-8+9446del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTGTG | T | 53 | a0001c0001t0001g0192a0001c0001t0001g0211a0001c0001t0001g0318others(50): Show | 53 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8+9443_-8+9446del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTGTGTG | T | 17 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0002g0026others(14): Show | 17 | HG02273.hp1 HG02809.hp2 HG03669.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+9441_-8+9446del others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTGTGTGT others(1): Show |
T | 98 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-8+9439_-8+9446del others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTGTGTGT others(3): Show |
T | 15 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(12): Show | 16 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+9437_-8+9446del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTGTGTGT others(5): Show |
T | 28 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0281others(25): Show | 28 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.-8+9435_-8+9446del others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTGTGTGT others(7): Show |
T | 8 | a0001c0001t0001g0048a0001c0001t0002g0129a0001c0001t0002g0130others(5): Show | 8 | HG00544.hp1 HG00621.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+9433_-8+9446del others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTGTGTGT others(9): Show |
T | 11 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0288others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+9431_-8+9446del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565572
|
TTGTGTGT others(13): Show |
T | 2 | a0001c0001t0008g0274a0002c0002t0004g0275 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-8+9427_-8+9446del others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565572 | |||||
| chr1:24565772
|
AT | A | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9611delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24565772 | |||||
| chr1:24565802
|
G | C | 40 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(37): Show | 40 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-8+9633G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565802 | ||||||
| chr1:24565851
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-8+9682T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565851 | ||||||
| chr1:24565896
|
A | C | 1 | a0001c0001t0002g0291 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-8+9727A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565896 | ||||||
| chr1:24565897
|
T | G | 1 | a0001c0001t0002g0138 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-8+9728T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565897 | ||||||
| chr1:24565963
|
A | G | 130 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8+9794A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24565963 | ||||||
| chr1:24566008
|
C | T | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9839C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566008 | ||||||
| chr1:24566044
|
G | T | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+9875G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566044 | ||||||
| chr1:24566056
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0003g0145a0002c0002t0013g0002others(1): Show | 5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+9887C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566056 | ||||||
| chr1:24566068
|
C | T | 261 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-8+9899C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566068 | ||||||
| chr1:24566325
|
T | C | 261 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-8+10156T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566325 | ||||||
| chr1:24566502
|
C | T | 48 | a0001c0001t0001g0144a0001c0001t0001g0281a0001c0001t0001g0282others(45): Show | 49 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-8+10333C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566502 | ||||||
| chr1:24566956
|
T | C | 1 | a0001c0001t0003g0385 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8+10787T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24566956 | ||||||
| chr1:24567005
|
G | T | 1 | a0001c0001t0002g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-8+10836G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567005 | ||||||
| chr1:24567105
|
C | T | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+10936C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567105 | ||||||
| chr1:24567178
|
C | T | 14 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(11): Show | 15 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8+11009C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567178 | ||||||
| chr1:24567181
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG01081.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-8+11012A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567181 | ||||||
| chr1:24567730
|
C | T | 142 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(139): Show | 143 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-8+11561C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567730 | ||||||
| chr1:24567741
|
C | G | 1 | a0001c0001t0003g0392 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-8+11572C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567741 | ||||||
| chr1:24567991
|
C | G | 31 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(28): Show | 31 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8+11822C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567991 | ||||||
| chr1:24567991
|
C | T | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+11822C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24567991 | ||||||
| chr1:24568180
|
C | T | 3 | a0001c0001t0008g0396a0001c0001t0032g0317a0002c0002t0004g0395 | 3 | HG01891.hp2 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+12011C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568180 | ||||||
| chr1:24568242
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-8+12073G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568242 | ||||||
| chr1:24568446
|
T | C | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12277T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568446 | ||||||
| chr1:24568506
|
G | A | 84 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+12337G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568506 | ||||||
| chr1:24568560
|
A | G | 150 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(147): Show | 152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-8+12391A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568560 | ||||||
| chr1:24568580
|
T | G | 84 | a0001c0001t0001g0028a0001c0001t0001g0298a0001c0001t0001g0299others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+12411T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568580 | ||||||
| chr1:24568612
|
G | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0001c0001t0001g0378 | 3 | HG01069.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-8+12443G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568612 | ||||||
| chr1:24568619
|
C | T | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12450C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568619 | ||||||
| chr1:24568696
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-8+12527G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568696 | ||||||
| chr1:24568762
|
T | C | 249 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-8+12593T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568762 | ||||||
| chr1:24568802
|
A | G | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12633A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568802 | ||||||
| chr1:24568820
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-8+12651G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568820 | ||||||
| chr1:24568820
|
G | T | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+12651G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568820 | ||||||
| chr1:24568903
|
A | G | 284 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-8+12734A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24568903 | ||||||
| chr1:24569001
|
T | C | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12832T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569001 | ||||||
| chr1:24569026
|
G | GT | 132 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-8+12866dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24569026 | |||||
| chr1:24569026
|
G | T | 2 | a0001c0001t0008g0274a0002c0002t0004g0275 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-8+12857G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569026 | ||||||
| chr1:24569026
|
GT | G | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12866delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24569026 | |||||
| chr1:24569031
|
T | G | 91 | a0001c0001t0001g0158a0001c0001t0001g0169a0001c0001t0001g0194others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-8+12862T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569031 | ||||||
| chr1:24569063
|
C | T | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12894C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569063 | ||||||
| chr1:24569092
|
C | A | 135 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8+12923C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569092 | ||||||
| chr1:24569097
|
A | G | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+12928A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569097 | ||||||
| chr1:24569155
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8+12986G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569155 | ||||||
| chr1:24569182
|
C | T | 1 | a0001c0001t0003g0010 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-8+13013C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569182 | ||||||
| chr1:24569238
|
C | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0169 | 2 | NA18961.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-8+13069C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569238 | ||||||
| chr1:24569252
|
CCAAAGTG others(5118): Show |
C | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+13115_-8+18239d others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24569252 | |||||
| chr1:24569253
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0137 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+13084C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569253 | ||||||
| chr1:24569257
|
G | A | 1 | a0001c0001t0003g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-8+13088G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569257 | ||||||
| chr1:24569314
|
A | G | 7 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(4): Show | 7 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+13145A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569314 | ||||||
| chr1:24569327
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-8+13158G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569327 | ||||||
| chr1:24569508
|
A | C | 1 | a0001c0001t0008g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+13339A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569508 | ||||||
| chr1:24569513
|
T | C | 1 | a0001c0001t0010g0059 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8+13344T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569513 | ||||||
| chr1:24569535
|
T | C | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8+13366T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569535 | ||||||
| chr1:24569554
|
T | C | 3 | a0001c0001t0008g0274a0001c0001t0032g0317a0002c0002t0004g0275 | 3 | HG02818.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+13385T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569554 | ||||||
| chr1:24569649
|
T | G | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0001c0001t0001g0378 | 3 | HG01069.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-8+13480T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569649 | ||||||
| chr1:24569671
|
C | T | 10 | a0001c0001t0001g0156a0001c0001t0001g0203a0001c0001t0001g0204others(7): Show | 10 | HG00438.hp2 HG00597.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+13502C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569671 | ||||||
| chr1:24569953
|
A | C | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+13784A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569953 | ||||||
| chr1:24569956
|
A | T | 2 | a0001c0001t0002g0116a0001c0001t0003g0333 | 2 | HG01255.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-8+13787A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24569956 | ||||||
| chr1:24570110
|
A | AT | 12 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0254others(9): Show | 12 | HG02027.hp2 HG02135.hp1 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8+13957dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24570110 | |||||
| chr1:24570377
|
T | C | 56 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+14208T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570377 | ||||||
| chr1:24570654
|
T | C | 1 | a0001c0001t0003g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-8+14485T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570654 | ||||||
| chr1:24570714
|
C | T | 7 | a0001c0001t0001g0048a0001c0001t0002g0129a0001c0001t0002g0130others(4): Show | 7 | HG00544.hp1 HG00621.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+14545C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570714 | ||||||
| chr1:24570818
|
C | T | 1 | a0001c0001t0003g0333 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-8+14649C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570818 | ||||||
| chr1:24570958
|
G | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | NA18954.hp2 NA18960.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+14789G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24570958 | ||||||
| chr1:24571076
|
G | A | 3 | a0001c0001t0001g0376a0001c0001t0001g0377a0001c0001t0001g0378 | 3 | HG01069.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-8+14907G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571076 | ||||||
| chr1:24571506
|
A | C | 3 | a0001c0001t0002g0086a0001c0001t0002g0095a0001c0001t0025g0087 | 3 | NA18963.hp2 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-8+15337A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571506 | ||||||
| chr1:24571580
|
C | T | 234 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-8+15411C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571580 | ||||||
| chr1:24571678
|
C | T | 2 | a0001c0001t0012g0202a0001c0001t0012g0215 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-8+15509C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571678 | ||||||
| chr1:24571760
|
G | A | 234 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-8+15591G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571760 | ||||||
| chr1:24571856
|
G | A | 1 | a0002c0002t0004g0395 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8+15687G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571856 | ||||||
| chr1:24571884
|
A | C | 56 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+15715A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571884 | ||||||
| chr1:24571886
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-8+15717G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571886 | ||||||
| chr1:24571962
|
C | T | 47 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0337others(44): Show | 47 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8+15793C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571962 | ||||||
| chr1:24571998
|
C | A | 47 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0337others(44): Show | 47 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8+15829C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24571998 | ||||||
| chr1:24572166
|
A | AAACC | 56 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+15999_-8+16000i others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24572166 | |||||
| chr1:24572448
|
G | C | 1 | a0001c0001t0001g0250 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-8+16279G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24572448 | ||||||
| chr1:24572857
|
A | G | 117 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-8+16688A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24572857 | ||||||
| chr1:24572999
|
C | T | 56 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+16830C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24572999 | ||||||
| chr1:24573039
|
T | C | 136 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8+16870T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573039 | ||||||
| chr1:24573120
|
T | C | 1 | a0001c0001t0014g0397 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-8+16951T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573120 | ||||||
| chr1:24573408
|
C | T | 44 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0337others(41): Show | 44 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+17239C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573408 | ||||||
| chr1:24573599
|
A | G | 1 | a0001c0001t0002g0279 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-8+17430A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573599 | ||||||
| chr1:24573600
|
GAAACAA | G | 56 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+17454_-8+17459d others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573600 | |||||
| chr1:24573835
|
T | C | 268 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(265): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-8+17666T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573835 | ||||||
| chr1:24573952
|
C | CA | 11 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0062others(8): Show | 11 | HG00408.hp1 HG00544.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+17802dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0324 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-8+17793_-8+17802d others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(4): Show |
16 | a0001c0001t0001g0340a0001c0001t0001g0367a0001c0001t0002g0349others(13): Show | 16 | HG00099.hp1 HG01074.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+17792_-8+17802d others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(5): Show |
17 | a0001c0001t0001g0323a0001c0001t0001g0337a0001c0001t0003g0219others(14): Show | 17 | HG00673.hp1 HG01433.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+17791_-8+17802d others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0003g0005a0001c0001t0003g0326a0001c0001t0003g0346others(4): Show | 7 | HG01106.hp1 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+17790_-8+17802d others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(7): Show |
8 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0377others(5): Show | 8 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+17789_-8+17802d others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(8): Show |
8 | a0001c0001t0001g0158a0001c0001t0001g0322a0001c0001t0001g0376others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+17788_-8+17802d others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0007g0297 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(15): Show |
12 | a0001c0001t0001g0167a0001c0001t0001g0181a0001c0001t0001g0188others(9): Show | 12 | HG00408.hp2 HG01109.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(16): Show |
21 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0178others(18): Show | 21 | HG00642.hp2 HG00673.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(25): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(17): Show |
8 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG01346.hp1 HG02040.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(18): Show |
4 | a0001c0001t0001g0192a0001c0001t0001g0205a0001c0001t0002g0197others(1): Show | 4 | HG00280.hp2 HG00438.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(27): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(19): Show |
4 | a0001c0001t0001g0309a0001c0001t0001g0313a0001c0001t0001g0314others(1): Show | 4 | NA18946.hp2 NA18971.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0302 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0298 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0221 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(31): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0224 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(33): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0311 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(38): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
CA | C | 102 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0078others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-8+17802delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
CAA | C | 30 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(27): Show | 30 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8+17801_-8+17802d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573952
|
CAAAAA | C | 41 | a0001c0001t0001g0318a0001c0001t0001g0331a0001c0001t0001g0332others(38): Show | 43 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-8+17798_-8+17802d others(7): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573952 | |||||
| chr1:24573962
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0028g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(25): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573962 | |||||
| chr1:24573969
|
A | AAAAAAAA others(24): Show |
3 | a0001c0001t0008g0007a0001c0001t0012g0154a0002c0002t0004g0201 | 3 | HG02109.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(33): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573969 | |||||
| chr1:24573969
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(32): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573969 | |||||
| chr1:24573969
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0012g0202a0001c0001t0012g0215 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-8+17802_-8+17803i others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24573969 | |||||
| chr1:24573971
|
A | AAAAAAAA others(14): Show |
1 | a0002c0002t0004g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573971 | ||||||
| chr1:24573971
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8+17802_-8+17803i others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24573971 | ||||||
| chr1:24574024
|
TCTC | T | 56 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+17858_-8+17860d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574024 | |||||
| chr1:24574078
|
C | T | 234 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-8+17909C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574078 | ||||||
| chr1:24574087
|
G | A | 56 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+17918G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574087 | ||||||
| chr1:24574092
|
C | T | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+17923C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574092 | ||||||
| chr1:24574128
|
G | GT | 11 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0337others(8): Show | 11 | HG00544.hp2 HG00673.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+17971dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574128 | |||||
| chr1:24574128
|
GT | G | 178 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(175): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-8+17971delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574128 | |||||
| chr1:24574133
|
T | C | 136 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8+17964T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574133 | ||||||
| chr1:24574168
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-8+17999C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574168 | ||||||
| chr1:24574190
|
C | A | 1 | a0001c0001t0011g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+18021C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574190 | ||||||
| chr1:24574210
|
C | A | 38 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0337others(35): Show | 38 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-8+18041C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574210 | ||||||
| chr1:24574230
|
T | C | 2 | a0001c0001t0011g0379a0001c0001t0011g0380 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+18061T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574230 | ||||||
| chr1:24574383
|
T | C | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+18214T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574383 | ||||||
| chr1:24574389
|
G | T | 6 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(3): Show | 6 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+18220G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574389 | ||||||
| chr1:24574461
|
G | T | 178 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(175): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-8+18292G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574461 | ||||||
| chr1:24574574
|
A | G | 6 | a0001c0001t0001g0400a0001c0001t0008g0396a0001c0001t0014g0397others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+18405A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574574 | ||||||
| chr1:24574626
|
T | C | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8+18457T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574626 | ||||||
| chr1:24574630
|
A | C | 178 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(175): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-8+18461A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574630 | ||||||
| chr1:24574689
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8+18520G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574689 | ||||||
| chr1:24574794
|
C | CT | 42 | a0001c0001t0001g0048a0001c0001t0001g0281a0001c0001t0001g0282others(39): Show | 42 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.-8+18644dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574794 | |||||
| chr1:24574794
|
CT | C | 10 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+18644delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574794 | |||||
| chr1:24574819
|
G | A | 48 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0337others(45): Show | 48 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.-8+18650G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574819 | ||||||
| chr1:24574858
|
T | C | 2 | a0001c0001t0003g0225a0001c0001t0003g0253 | 2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-8+18689T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574858 | ||||||
| chr1:24574929
|
G | A | 4 | a0001c0001t0002g0045a0001c0001t0002g0117a0001c0001t0002g0118others(1): Show | 4 | NA18972.hp1 NA18986.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+18760G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24574929 | ||||||
| chr1:24574941
|
A | AC | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8+18774dupC | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24574941 | |||||
| chr1:24575005
|
G | C | 47 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0337others(44): Show | 47 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8+18836G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575005 | ||||||
| chr1:24575015
|
C | T | 44 | a0001c0001t0001g0144a0001c0001t0001g0318a0001c0001t0001g0331others(41): Show | 46 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-8+18846C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575015 | ||||||
| chr1:24575244
|
C | A | 1 | a0001c0001t0003g0225 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-8+19075C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575244 | ||||||
| chr1:24575341
|
T | C | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+19172T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575341 | ||||||
| chr1:24575344
|
C | T | 3 | a0001c0001t0002g0086a0001c0001t0002g0095a0001c0001t0025g0087 | 3 | NA18963.hp2 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-8+19175C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575344 | ||||||
| chr1:24575353
|
A | G | 249 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-8+19184A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575353 | ||||||
| chr1:24575359
|
A | G | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8+19190A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575359 | ||||||
| chr1:24575372
|
T | G | 180 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(177): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-8+19203T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575372 | ||||||
| chr1:24575379
|
G | T | 4 | a0001c0001t0001g0400a0001c0001t0014g0397a0001c0001t0014g0398others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+19210G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575379 | ||||||
| chr1:24575480
|
G | A | 56 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+19311G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575480 | ||||||
| chr1:24575493
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-8+19324G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575493 | ||||||
| chr1:24575507
|
T | G | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-8+19338T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575507 | ||||||
| chr1:24575535
|
A | T | 4 | a0001c0001t0008g0022a0002c0002t0004g0023a0002c0002t0004g0025others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+19366A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575535 | ||||||
| chr1:24575552
|
C | T | 250 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-8+19383C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575552 | ||||||
| chr1:24575585
|
C | T | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+19416C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575585 | ||||||
| chr1:24575718
|
G | A | 32 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(29): Show | 32 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.-8+19549G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575718 | ||||||
| chr1:24575760
|
G | A | 282 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-8+19591G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575760 | ||||||
| chr1:24575903
|
C | T | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19521C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24575903 | ||||||
| chr1:24575915
|
C | CA | 10 | a0001c0001t0001g0158a0001c0001t0001g0178a0001c0001t0001g0186others(7): Show | 10 | HG01081.hp2 HG01175.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-19483dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | |||||
| chr1:24575915
|
CA | C | 182 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(179): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-7-19483delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | |||||
| chr1:24575915
|
CAA | C | 35 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0058others(32): Show | 35 | HG00323.hp1 HG00558.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-7-19484_-7-19483d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | |||||
| chr1:24575915
|
CAAAAAA | C | 55 | a0001c0001t0001g0028a0001c0001t0001g0323a0001c0001t0001g0324others(52): Show | 55 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-7-19488_-7-19483d others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | |||||
| chr1:24575915
|
CAAAAAAA | C | 11 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7-19489_-7-19483d others(9): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | |||||
| chr1:24575915
|
CAAAAAAA others(3): Show |
C | 12 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-19492_-7-19483d others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24575915 | |||||
| chr1:24576015
|
A | G | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19409A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576015 | ||||||
| chr1:24576038
|
C | T | 1 | a0001c0001t0002g0361 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-7-19386C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576038 | ||||||
| chr1:24576063
|
G | A | 37 | a0001c0001t0001g0318a0001c0001t0001g0331a0001c0001t0001g0332others(34): Show | 38 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-7-19361G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576063 | ||||||
| chr1:24576119
|
C | T | 2 | a0001c0001t0008g0274a0002c0002t0004g0275 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-19305C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576119 | ||||||
| chr1:24576209
|
G | A | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19215G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576209 | ||||||
| chr1:24576295
|
A | G | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19129A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576295 | ||||||
| chr1:24576296
|
C | T | 181 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(178): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.-7-19128C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576296 | ||||||
| chr1:24576297
|
G | A | 9 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-19127G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576297 | ||||||
| chr1:24576320
|
C | T | 2 | a0001c0001t0011g0379a0001c0001t0011g0380 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-19104C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576320 | ||||||
| chr1:24576343
|
C | G | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-19081C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576343 | ||||||
| chr1:24576434
|
C | T | 13 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(10): Show | 13 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-18990C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576434 | ||||||
| chr1:24576514
|
A | G | 32 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(29): Show | 32 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.-7-18910A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576514 | ||||||
| chr1:24576555
|
A | G | 47 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0337others(44): Show | 47 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-7-18869A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576555 | ||||||
| chr1:24576662
|
G | T | 2 | a0001c0001t0008g0274a0002c0002t0004g0275 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-18762G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576662 | ||||||
| chr1:24576745
|
A | G | 1 | a0001c0001t0003g0385 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7-18679A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576745 | ||||||
| chr1:24576752
|
G | T | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-18672G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576752 | ||||||
| chr1:24576852
|
A | G | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-18572A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576852 | ||||||
| chr1:24576866
|
A | G | 69 | a0001c0001t0001g0028a0001c0001t0001g0322a0001c0001t0001g0323others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7-18558A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576866 | ||||||
| chr1:24576904
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-7-18520G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576904 | ||||||
| chr1:24576938
|
G | T | 2 | a0001c0001t0003g0069a0001c0001t0003g0074 | 2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-7-18486G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576938 | ||||||
| chr1:24576981
|
C | A | 180 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(177): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-7-18443C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576981 | ||||||
| chr1:24576983
|
A | C | 101 | a0001c0001t0001g0028a0001c0001t0001g0281a0001c0001t0001g0282others(98): Show | 101 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.-7-18441A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576983 | ||||||
| chr1:24576999
|
G | A | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-18425G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24576999 | ||||||
| chr1:24577094
|
C | T | 6 | a0001c0001t0001g0400a0001c0001t0008g0396a0001c0001t0014g0397others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-18330C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577094 | ||||||
| chr1:24577177
|
T | A | 6 | a0001c0001t0001g0400a0001c0001t0008g0396a0001c0001t0014g0397others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-18247T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577177 | ||||||
| chr1:24577197
|
G | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0094 | 2 | NA18983.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-7-18227G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577197 | ||||||
| chr1:24577401
|
G | GT | 66 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055others(63): Show | 66 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-7-17993dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | |||||
| chr1:24577401
|
G | GTT | 29 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0286others(26): Show | 30 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-7-17994_-7-17993d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | |||||
| chr1:24577401
|
G | GTTT | 14 | a0001c0001t0001g0332a0001c0001t0003g0010a0001c0001t0003g0011others(11): Show | 14 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-17995_-7-17993d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | |||||
| chr1:24577401
|
GT | G | 26 | a0001c0001t0001g0127a0001c0001t0001g0156a0001c0001t0001g0161others(23): Show | 26 | HG00438.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7-17993delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | |||||
| chr1:24577401
|
GTT | G | 32 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0181others(29): Show | 32 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.-7-17994_-7-17993d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | |||||
| chr1:24577401
|
GTTTT | G | 12 | a0001c0001t0001g0028a0001c0001t0001g0323a0001c0001t0006g0327others(9): Show | 12 | HG01099.hp2 HG01884.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-17996_-7-17993d others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577401 | |||||
| chr1:24577404
|
T | TTTTTTTG | 32 | a0001c0001t0001g0324a0001c0001t0001g0337a0001c0001t0001g0340others(29): Show | 32 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-7-18014_-7-18013i others(9): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24577404 | |||||
| chr1:24577414
|
T | G | 1 | a0001c0001t0008g0396 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-7-18010T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577414 | ||||||
| chr1:24577415
|
T | G | 3 | a0001c0001t0001g0323a0001c0001t0006g0327a0001c0001t0006g0366 | 3 | HG02886.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-7-18009T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577415 | ||||||
| chr1:24577416
|
T | G | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-18008T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577416 | ||||||
| chr1:24577417
|
T | G | 1 | a0001c0001t0001g0400 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7-18007T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577417 | ||||||
| chr1:24577420
|
T | G | 29 | a0001c0001t0001g0324a0001c0001t0001g0337a0001c0001t0001g0340others(26): Show | 29 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7-18004T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577420 | ||||||
| chr1:24577637
|
T | C | 1 | a0001c0001t0001g0376 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7-17787T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577637 | ||||||
| chr1:24577764
|
G | A | 308 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-7-17660G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577764 | ||||||
| chr1:24577883
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-7-17541G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577883 | ||||||
| chr1:24577919
|
G | A | 199 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-7-17505G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577919 | ||||||
| chr1:24577963
|
T | C | 139 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-7-17461T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577963 | ||||||
| chr1:24577970
|
T | G | 151 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(148): Show | 151 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-7-17454T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24577970 | ||||||
| chr1:24578012
|
CAGCACTT others(4): Show |
C | 2 | a0001c0001t0015g0008a0001c0001t0015g0009 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-7-17409_-7-17399d others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578012 | |||||
| chr1:24578021
|
G | T | 10 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-17403G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578021 | ||||||
| chr1:24578109
|
A | G | 3 | a0001c0001t0003g0387a0001c0001t0015g0008a0001c0001t0015g0009 | 3 | HG02630.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-7-17315A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578109 | ||||||
| chr1:24578245
|
C | CA | 153 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0125others(150): Show | 154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-7-17159dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578245 | |||||
| chr1:24578245
|
C | CAA | 113 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0048others(110): Show | 113 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-7-17160_-7-17159d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578245 | |||||
| chr1:24578245
|
C | CAAA | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0002g0080others(8): Show | 11 | HG00735.hp2 HG01243.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-17161_-7-17159d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578245 | |||||
| chr1:24578245
|
CA | C | 22 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(19): Show | 22 | HG01175.hp1 HG01256.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-17159delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578245 | |||||
| chr1:24578371
|
G | C | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-17053G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578371 | ||||||
| chr1:24578425
|
C | A | 2 | a0001c0001t0001g0121a0001c0001t0002g0213 | 2 | HG00558.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-7-16999C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578425 | ||||||
| chr1:24578469
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0003c0003t0027g0276 | 3 | HG01243.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-7-16955G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578469 | ||||||
| chr1:24578534
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0003g0053 | 3 | HG02630.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-7-16890G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578534 | ||||||
| chr1:24578541
|
G | GTTTTCT | 14 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-16874_-7-16869d others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578541 | |||||
| chr1:24578551
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7-16873T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578551 | ||||||
| chr1:24578560
|
C | CT | 7 | a0001c0001t0001g0037a0001c0001t0001g0139a0001c0001t0001g0267others(4): Show | 7 | HG00408.hp1 HG03490.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-16844dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578560 | |||||
| chr1:24578560
|
C | T | 12 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-16864C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578560 | ||||||
| chr1:24578560
|
CT | C | 40 | a0001c0001t0001g0028a0001c0001t0001g0105a0001c0001t0001g0235others(37): Show | 40 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-7-16844delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578560 | |||||
| chr1:24578560
|
CTT | C | 80 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0144others(77): Show | 81 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-7-16845_-7-16844d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24578560 | |||||
| chr1:24578563
|
T | TC | 16 | a0001c0001t0002g0279a0001c0001t0002g0291a0001c0001t0002g0292others(13): Show | 16 | HG00558.hp1 HG01167.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7-16861_-7-16860i others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578563 | ||||||
| chr1:24578564
|
T | C | 2 | a0001c0001t0002g0294a0001c0001t0006g0141 | 2 | HG01256.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-16860T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578564 | ||||||
| chr1:24578699
|
A | G | 6 | a0001c0001t0001g0222a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG00323.hp2 HG01175.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-16725A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578699 | ||||||
| chr1:24578748
|
G | C | 99 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0104others(96): Show | 99 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-7-16676G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578748 | ||||||
| chr1:24578789
|
G | A | 4 | a0001c0001t0003g0392a0001c0001t0003g0394a0001c0001t0008g0274others(1): Show | 4 | HG02818.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-16635G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578789 | ||||||
| chr1:24578804
|
C | A | 83 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0144others(80): Show | 84 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-7-16620C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578804 | ||||||
| chr1:24578844
|
G | A | 15 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(12): Show | 15 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-16580G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578844 | ||||||
| chr1:24578883
|
A | G | 1 | a0001c0001t0003g0348 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-7-16541A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24578883 | ||||||
| chr1:24579018
|
G | A | 104 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0104others(101): Show | 104 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-7-16406G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579018 | ||||||
| chr1:24579025
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-7-16399C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579025 | ||||||
| chr1:24579026
|
G | A | 1 | a0001c0001t0003g0387 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-16398G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579026 | ||||||
| chr1:24579026
|
G | T | 5 | a0001c0001t0002g0245a0001c0001t0002g0247a0001c0001t0002g0248others(2): Show | 5 | HG00423.hp2 HG02080.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-16398G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579026 | ||||||
| chr1:24579038
|
C | T | 1 | a0001c0001t0003g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-16386C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579038 | ||||||
| chr1:24579054
|
G | A | 1 | a0001c0001t0003g0333 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-7-16370G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579054 | ||||||
| chr1:24579133
|
G | C | 134 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0056others(131): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-7-16291G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579133 | ||||||
| chr1:24579169
|
G | T | 2 | a0001c0001t0002g0136a0001c0001t0002g0197 | 2 | NA18951.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-7-16255G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579169 | ||||||
| chr1:24579176
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7-16248G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579176 | ||||||
| chr1:24579192
|
TG | T | 116 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0144others(113): Show | 118 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-16227delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24579192 | |||||
| chr1:24579197
|
G | GT | 7 | a0001c0001t0001g0254a0001c0001t0002g0036a0001c0001t0002g0045others(4): Show | 7 | HG00544.hp2 HG02027.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-16214dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24579197 | |||||
| chr1:24579197
|
G | T | 19 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(16): Show | 19 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-16227G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579197 | ||||||
| chr1:24579197
|
GT | G | 7 | a0001c0001t0002g0117a0001c0001t0003g0005a0001c0001t0011g0273others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-16214delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24579197 | |||||
| chr1:24579197
|
GTT | G | 44 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0323others(41): Show | 44 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-7-16215_-7-16214d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24579197 | |||||
| chr1:24579266
|
G | C | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-16158G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579266 | ||||||
| chr1:24579610
|
C | T | 16 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(13): Show | 16 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-15814C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579610 | ||||||
| chr1:24579648
|
G | T | 4 | a0001c0001t0001g0144a0001c0001t0003g0145a0002c0002t0013g0002others(1): Show | 5 | HG02723.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-15776G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579648 | ||||||
| chr1:24579829
|
C | T | 12 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-15595C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579829 | ||||||
| chr1:24579838
|
T | G | 4 | a0001c0001t0008g0396a0001c0001t0015g0008a0001c0001t0015g0009others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-15586T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24579838 | ||||||
| chr1:24580002
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-7-15422G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580002 | ||||||
| chr1:24580071
|
A | C | 16 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(13): Show | 16 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-15353A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580071 | ||||||
| chr1:24580122
|
G | A | 3 | a0001c0001t0001g0323a0001c0001t0006g0327a0001c0001t0006g0366 | 3 | HG02886.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-7-15302G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580122 | ||||||
| chr1:24580145
|
G | A | 2 | a0001c0001t0002g0349a0001c0001t0019g0347 | 2 | HG02015.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-7-15279G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580145 | ||||||
| chr1:24580185
|
C | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0003g0387others(1): Show | 4 | HG02572.hp2 HG03486.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-15239C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580185 | ||||||
| chr1:24580186
|
G | A | 6 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(3): Show | 6 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-15238G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580186 | ||||||
| chr1:24580220
|
A | G | 303 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(300): Show | 305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.-7-15204A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580220 | ||||||
| chr1:24580227
|
A | G | 134 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0056others(131): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-7-15197A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580227 | ||||||
| chr1:24580398
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-7-15026C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580398 | ||||||
| chr1:24580434
|
C | T | 2 | a0001c0001t0003g0373a0001c0001t0003g0374 | 2 | HG02080.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-7-14990C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580434 | ||||||
| chr1:24580599
|
C | T | 1 | a0001c0001t0002g0342 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-7-14825C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580599 | ||||||
| chr1:24580751
|
G | A | 73 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0144others(70): Show | 74 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-7-14673G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580751 | ||||||
| chr1:24580769
|
T | C | 2 | a0001c0001t0003g0387a0001c0001t0032g0317 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-14655T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580769 | ||||||
| chr1:24580924
|
G | A | 291 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0048others(288): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.-7-14500G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580924 | ||||||
| chr1:24580964
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-7-14460C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24580964 | ||||||
| chr1:24581029
|
C | T | 2 | a0001c0001t0003g0392a0001c0001t0003g0394 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-14395C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581029 | ||||||
| chr1:24581052
|
G | C | 36 | a0001c0001t0002g0342a0001c0001t0002g0361a0001c0001t0003g0010others(33): Show | 37 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-7-14372G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581052 | ||||||
| chr1:24581122
|
C | CT | 29 | a0001c0001t0001g0227a0001c0001t0001g0322a0001c0001t0001g0376others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7-14289dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24581122 | |||||
| chr1:24581188
|
C | T | 1 | a0001c0001t0003g0375 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-7-14236C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581188 | ||||||
| chr1:24581242
|
A | G | 299 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(296): Show | 301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.-7-14182A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581242 | ||||||
| chr1:24581244
|
A | G | 330 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(327): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.-7-14180A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581244 | ||||||
| chr1:24581304
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-7-14120A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581304 | ||||||
| chr1:24581969
|
A | G | 1 | a0001c0001t0003g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-7-13455A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24581969 | ||||||
| chr1:24582021
|
A | T | 14 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-13403A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582021 | ||||||
| chr1:24582031
|
G | T | 3 | a0001c0001t0011g0273a0001c0001t0011g0379a0001c0001t0011g0380 | 3 | HG01891.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-13393G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582031 | ||||||
| chr1:24582044
|
T | C | 45 | a0001c0001t0001g0323a0001c0001t0002g0342a0001c0001t0002g0361others(42): Show | 46 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-7-13380T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582044 | ||||||
| chr1:24582128
|
T | G | 133 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0002g0021others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-7-13296T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582128 | ||||||
| chr1:24582134
|
A | C | 133 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0002g0021others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-7-13290A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582134 | ||||||
| chr1:24582198
|
C | T | 2 | a0001c0001t0003g0256a0001c0001t0003g0258 | 2 | HG00544.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-7-13226C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582198 | ||||||
| chr1:24582292
|
C | T | 262 | a0001c0001t0001g0037a0001c0001t0001g0104a0001c0001t0001g0121others(259): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.-7-13132C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582292 | ||||||
| chr1:24582438
|
C | T | 62 | a0001c0001t0001g0028a0001c0001t0001g0144a0001c0001t0001g0323others(59): Show | 64 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.-7-12986C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582438 | ||||||
| chr1:24582468
|
G | A | 156 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(153): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-7-12956G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582468 | ||||||
| chr1:24582596
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0140 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-12828C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582596 | ||||||
| chr1:24582691
|
T | C | 1 | a0001c0001t0003g0333 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-7-12733T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582691 | ||||||
| chr1:24582707
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-7-12717A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582707 | ||||||
| chr1:24582768
|
C | T | 3 | a0001c0001t0011g0273a0001c0001t0011g0379a0001c0001t0011g0380 | 3 | HG01891.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-7-12656C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582768 | ||||||
| chr1:24582810
|
G | T | 72 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0156others(69): Show | 72 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-7-12614G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582810 | ||||||
| chr1:24582817
|
T | TCCTA | 43 | a0001c0001t0001g0323a0001c0001t0002g0342a0001c0001t0002g0361others(40): Show | 44 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.-7-12606_-7-12603d others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24582817 | |||||
| chr1:24582912
|
T | C | 47 | a0001c0001t0001g0340a0001c0001t0002g0349a0001c0001t0003g0070others(44): Show | 47 | HG00099.hp1 HG00558.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-7-12512T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24582912 | ||||||
| chr1:24583002
|
A | T | 1 | a0001c0001t0003g0093 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-7-12422A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583002 | ||||||
| chr1:24583051
|
C | T | 1 | a0002c0002t0004g0030 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-7-12373C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583051 | ||||||
| chr1:24583243
|
CAG | C | 101 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0055others(98): Show | 102 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-7-12176_-7-12175d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24583243 | |||||
| chr1:24583287
|
G | T | 1 | a0001c0001t0003g0385 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7-12137G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583287 | ||||||
| chr1:24583466
|
C | A | 3 | a0001c0001t0001g0250a0001c0001t0001g0313a0001c0001t0005g0312 | 3 | NA18971.hp2 NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-7-11958C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583466 | ||||||
| chr1:24583584
|
C | T | 207 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0055others(204): Show | 208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.-7-11840C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583584 | ||||||
| chr1:24583717
|
G | GA | 76 | a0001c0001t0001g0037a0001c0001t0001g0125a0001c0001t0001g0155others(73): Show | 76 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-7-11686dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24583717 | |||||
| chr1:24583717
|
GA | G | 50 | a0001c0001t0001g0340a0001c0001t0001g0400a0001c0001t0002g0349others(47): Show | 50 | HG00099.hp1 HG00558.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-7-11686delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24583717 | |||||
| chr1:24583717
|
GAA | G | 42 | a0001c0001t0001g0323a0001c0001t0002g0342a0001c0001t0002g0361others(39): Show | 43 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-7-11687_-7-11686d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24583717 | |||||
| chr1:24583719
|
A | G | 1 | a0001c0001t0003g0147 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7-11705A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583719 | ||||||
| chr1:24583720
|
A | G | 42 | a0001c0001t0001g0323a0001c0001t0002g0342a0001c0001t0002g0361others(39): Show | 43 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-7-11704A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583720 | ||||||
| chr1:24583793
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-11631C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583793 | ||||||
| chr1:24583828
|
T | C | 208 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0055others(205): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-7-11596T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583828 | ||||||
| chr1:24583840
|
T | A | 5 | a0001c0001t0002g0045a0001c0001t0002g0052a0001c0001t0002g0117others(2): Show | 5 | NA18960.hp2 NA18972.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-11584T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24583840 | ||||||
| chr1:24584096
|
A | G | 1 | a0001c0001t0011g0379 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7-11328A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584096 | ||||||
| chr1:24584176
|
T | C | 5 | a0001c0001t0008g0150a0001c0001t0008g0396a0001c0001t0015g0008others(2): Show | 5 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-11248T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584176 | ||||||
| chr1:24584196
|
G | A | 2 | a0001c0001t0002g0035a0001c0001t0002g0072 | 2 | NA19002.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-7-11228G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584196 | ||||||
| chr1:24584236
|
A | T | 1 | a0001c0001t0003g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-7-11188A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584236 | ||||||
| chr1:24584437
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-7-10987G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584437 | ||||||
| chr1:24584601
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0003c0003t0027g0276 | 3 | HG01243.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-7-10823C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584601 | ||||||
| chr1:24584723
|
G | T | 18 | a0001c0001t0001g0028a0001c0001t0001g0144a0001c0001t0008g0022others(15): Show | 19 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-10701G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584723 | ||||||
| chr1:24584829
|
G | A | 4 | a0001c0001t0001g0400a0001c0001t0014g0397a0001c0001t0014g0398others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-10595G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584829 | ||||||
| chr1:24584938
|
C | T | 5 | a0001c0001t0002g0045a0001c0001t0002g0052a0001c0001t0002g0117others(2): Show | 5 | NA18960.hp2 NA18972.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-10486C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584938 | ||||||
| chr1:24584974
|
CGGGTGGG others(9): Show |
C | 12 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0006g0141others(9): Show | 12 | HG00558.hp1 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-10448_-7-10433d others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24584974 | |||||
| chr1:24584991
|
G | A | 207 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0055others(204): Show | 208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.-7-10433G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584991 | ||||||
| chr1:24584997
|
G | A | 3 | a0001c0001t0003g0226a0001c0001t0003g0325a0001c0001t0003g0338 | 3 | HG02056.hp1 HG02135.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-7-10427G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584997 | ||||||
| chr1:24584999
|
G | T | 1 | a0001c0001t0018g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-10425G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24584999 | ||||||
| chr1:24585120
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0003c0003t0027g0276 | 3 | HG01243.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-7-10304G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585120 | ||||||
| chr1:24585147
|
CT | C | 3 | a0001c0001t0009g0032a0001c0001t0009g0065a0001c0001t0009g0067 | 3 | HG02055.hp2 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-7-10274delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24585147 | |||||
| chr1:24585269
|
G | T | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-10155G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585269 | ||||||
| chr1:24585434
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0286a0001c0001t0001g0322 | 3 | HG03490.hp2 HG03492.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-9990G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585434 | ||||||
| chr1:24585568
|
G | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0140 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-9856G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585568 | ||||||
| chr1:24585589
|
T | G | 170 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0156others(167): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-7-9835T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585589 | ||||||
| chr1:24585679
|
G | A | 9 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0322others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-9745G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585679 | ||||||
| chr1:24585890
|
G | A | 2 | a0001c0001t0015g0008a0001c0001t0015g0009 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-7-9534G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585890 | ||||||
| chr1:24585978
|
C | T | 37 | a0001c0001t0001g0340a0001c0001t0002g0349a0001c0001t0003g0070others(34): Show | 37 | HG00099.hp1 HG01074.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7-9446C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24585978 | ||||||
| chr1:24586037
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-7-9387C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586037 | ||||||
| chr1:24586219
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0112others(3): Show | 6 | HG01070.hp2 HG01361.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-9205G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586219 | ||||||
| chr1:24586281
|
C | A | 1 | a0001c0001t0007g0272 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-7-9143C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586281 | ||||||
| chr1:24586300
|
G | T | 1 | a0001c0001t0002g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-7-9124G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586300 | ||||||
| chr1:24586393
|
G | A | 62 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(59): Show | 63 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-7-9031G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586393 | ||||||
| chr1:24586532
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-7-8892G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586532 | ||||||
| chr1:24586538
|
G | A | 37 | a0001c0001t0001g0340a0001c0001t0002g0349a0001c0001t0003g0070others(34): Show | 37 | HG00099.hp1 HG01074.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7-8886G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586538 | ||||||
| chr1:24586586
|
C | A | 1 | a0001c0001t0003g0372 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-7-8838C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586586 | ||||||
| chr1:24586596
|
A | G | 22 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(19): Show | 22 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-8828A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586596 | ||||||
| chr1:24586619
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-7-8805G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586619 | ||||||
| chr1:24586737
|
G | A | 141 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0055others(138): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-7-8687G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586737 | ||||||
| chr1:24586747
|
G | A | 1 | a0001c0001t0008g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-8677G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586747 | ||||||
| chr1:24586759
|
C | CA | 40 | a0001c0001t0001g0158a0001c0001t0001g0169a0001c0001t0001g0261others(37): Show | 40 | HG00099.hp1 HG01074.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.-7-8647dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24586759 | |||||
| chr1:24586759
|
CA | C | 177 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0061others(174): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-7-8647delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24586759 | |||||
| chr1:24586849
|
TG | T | 21 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(18): Show | 21 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-8570delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24586849 | |||||
| chr1:24586930
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-7-8494C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586930 | ||||||
| chr1:24586972
|
C | T | 319 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(316): Show | 321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.-7-8452C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24586972 | ||||||
| chr1:24587066
|
G | T | 1 | a0001c0001t0002g0052 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-7-8358G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587066 | ||||||
| chr1:24587249
|
G | C | 13 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(10): Show | 13 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-8175G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587249 | ||||||
| chr1:24587337
|
T | C | 4 | a0001c0001t0001g0400a0001c0001t0014g0397a0001c0001t0014g0398others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-8087T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587337 | ||||||
| chr1:24587404
|
T | C | 5 | a0001c0001t0008g0150a0001c0001t0008g0396a0001c0001t0015g0008others(2): Show | 5 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-8020T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587404 | ||||||
| chr1:24587481
|
C | A | 42 | a0001c0001t0001g0323a0001c0001t0002g0342a0001c0001t0002g0361others(39): Show | 43 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-7-7943C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587481 | ||||||
| chr1:24587496
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-7-7928G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587496 | ||||||
| chr1:24587541
|
A | T | 278 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(275): Show | 279 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-7-7883A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587541 | ||||||
| chr1:24587588
|
A | G | 75 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0156others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-7-7836A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587588 | ||||||
| chr1:24587666
|
A | G | 1 | a0001c0001t0008g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7-7758A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587666 | ||||||
| chr1:24587749
|
G | A | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-7675G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587749 | ||||||
| chr1:24587934
|
CTTTTTCT others(5): Show |
C | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-7472_-7-7461del others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24587934 | |||||
| chr1:24587985
|
G | A | 21 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(18): Show | 21 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-7439G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24587985 | ||||||
| chr1:24588016
|
GA | G | 3 | a0001c0001t0001g0323a0001c0001t0006g0327a0001c0001t0006g0366 | 3 | HG02886.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-7-7405delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24588016 | |||||
| chr1:24588027
|
A | G | 2 | a0001c0001t0003g0219a0001c0001t0003g0346 | 2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-7-7397A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588027 | ||||||
| chr1:24588188
|
T | C | 63 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(60): Show | 64 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.-7-7236T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588188 | ||||||
| chr1:24588442
|
A | G | 2 | a0001c0001t0003g0010a0001c0001t0003g0011 | 2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7-6982A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588442 | ||||||
| chr1:24588460
|
G | A | 1 | a0001c0001t0003g0092 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-7-6964G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588460 | ||||||
| chr1:24588757
|
G | T | 37 | a0001c0001t0002g0342a0001c0001t0002g0361a0001c0001t0003g0012others(34): Show | 38 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-7-6667G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24588757 | ||||||
| chr1:24589266
|
G | T | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-7-6158G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589266 | ||||||
| chr1:24589290
|
C | G | 160 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(157): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-7-6134C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589290 | ||||||
| chr1:24589290
|
CGTTTGAT others(6): Show |
C | 7 | a0001c0001t0003g0392a0001c0001t0003g0394a0001c0001t0008g0150others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-6131_-7-6119del others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24589290 | |||||
| chr1:24589308
|
T | C | 7 | a0001c0001t0003g0392a0001c0001t0003g0394a0001c0001t0008g0150others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-6116T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589308 | ||||||
| chr1:24589438
|
T | A | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-5986T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589438 | ||||||
| chr1:24589493
|
T | C | 151 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(148): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-7-5931T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589493 | ||||||
| chr1:24589635
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0003g0053 | 3 | HG02630.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-7-5789G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589635 | ||||||
| chr1:24589731
|
G | A | 1 | a0001c0001t0003g0334 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-7-5693G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589731 | ||||||
| chr1:24589734
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-7-5690G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589734 | ||||||
| chr1:24589788
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-7-5636G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589788 | ||||||
| chr1:24589818
|
G | T | 1 | a0001c0001t0008g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-5606G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589818 | ||||||
| chr1:24589876
|
G | A | 1 | a0001c0001t0003g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-7-5548G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589876 | ||||||
| chr1:24589932
|
C | G | 56 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0056others(53): Show | 57 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.-7-5492C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24589932 | ||||||
| chr1:24590000
|
A | T | 1 | a0001c0001t0008g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-5424A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590000 | ||||||
| chr1:24590046
|
C | A | 1 | a0001c0001t0003g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-7-5378C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590046 | ||||||
| chr1:24590363
|
C | T | 2 | a0001c0001t0008g0274a0003c0003t0027g0276 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-5061C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590363 | ||||||
| chr1:24590492
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-7-4932G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590492 | ||||||
| chr1:24590706
|
C | G | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-4718C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590706 | ||||||
| chr1:24590870
|
A | C | 1 | a0002c0002t0004g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-7-4554A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590870 | ||||||
| chr1:24590872
|
T | C | 123 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0261others(120): Show | 123 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-7-4552T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590872 | ||||||
| chr1:24590965
|
G | T | 43 | a0001c0001t0003g0070a0001c0001t0003g0076a0001c0001t0003g0077others(40): Show | 43 | HG00099.hp1 HG00639.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.-7-4459G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24590965 | ||||||
| chr1:24591005
|
A | G | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-4419A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591005 | ||||||
| chr1:24591038
|
G | C | 1 | a0001c0001t0006g0151 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-7-4386G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591038 | ||||||
| chr1:24591052
|
A | G | 198 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(195): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-7-4372A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591052 | ||||||
| chr1:24591053
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-7-4371C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591053 | ||||||
| chr1:24591062
|
AG | A | 76 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-7-4360delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24591062 | |||||
| chr1:24591064
|
G | C | 76 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-7-4360G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591064 | ||||||
| chr1:24591105
|
T | C | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-4319T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591105 | ||||||
| chr1:24591133
|
C | T | 20 | a0001c0001t0001g0028a0001c0001t0003g0392a0001c0001t0003g0394others(17): Show | 21 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-4291C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591133 | ||||||
| chr1:24591254
|
C | T | 4 | a0001c0001t0001g0400a0001c0001t0014g0397a0001c0001t0014g0398others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-4170C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591254 | ||||||
| chr1:24591382
|
C | T | 17 | a0001c0001t0001g0028a0001c0001t0003g0392a0001c0001t0003g0394others(14): Show | 17 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7-4042C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591382 | ||||||
| chr1:24591412
|
C | T | 3 | a0001c0001t0003g0005a0002c0002t0004g0004a0002c0002t0004g0006 | 3 | HG01106.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-7-4012C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591412 | ||||||
| chr1:24591515
|
A | G | 3 | a0001c0001t0003g0392a0001c0001t0003g0394a0002c0002t0004g0017 | 3 | HG01243.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-3909A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591515 | ||||||
| chr1:24591575
|
T | A | 1 | a0001c0001t0024g0101 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-7-3849T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591575 | ||||||
| chr1:24591712
|
G | T | 15 | a0001c0001t0001g0028a0001c0001t0008g0022a0002c0002t0004g0023others(12): Show | 15 | HG01099.hp2 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-3712G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591712 | ||||||
| chr1:24591765
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-7-3659G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591765 | ||||||
| chr1:24591817
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-7-3607G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24591817 | ||||||
| chr1:24592079
|
C | T | 1 | a0002c0002t0004g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-7-3345C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592079 | ||||||
| chr1:24592244
|
C | T | 79 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(76): Show | 79 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-7-3180C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592244 | ||||||
| chr1:24592245
|
G | A | 4 | a0001c0001t0001g0400a0001c0001t0014g0397a0001c0001t0014g0398others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-3179G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592245 | ||||||
| chr1:24592248
|
A | G | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-3176A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592248 | ||||||
| chr1:24592364
|
C | G | 22 | a0001c0001t0003g0074a0001c0001t0003g0179a0001c0001t0003g0225others(19): Show | 22 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-3060C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592364 | ||||||
| chr1:24592632
|
A | T | 211 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(208): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.-7-2792A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592632 | ||||||
| chr1:24592745
|
C | T | 9 | a0001c0001t0001g0400a0001c0001t0008g0274a0001c0001t0008g0396others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-2679C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592745 | ||||||
| chr1:24592812
|
G | A | 6 | a0001c0001t0002g0039a0001c0001t0002g0041a0001c0001t0002g0115others(3): Show | 6 | HG01081.hp1 NA18951.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-2612G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592812 | ||||||
| chr1:24592835
|
C | A | 1 | a0001c0001t0003g0089 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-7-2589C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592835 | ||||||
| chr1:24592835
|
C | T | 91 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(88): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-7-2589C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592835 | ||||||
| chr1:24592850
|
C | T | 1 | a0001c0001t0001g0376 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7-2574C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592850 | ||||||
| chr1:24592851
|
G | A | 1 | a0001c0001t0003g0351 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-7-2573G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592851 | ||||||
| chr1:24592854
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-7-2570G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592854 | ||||||
| chr1:24592923
|
T | A | 2 | a0001c0001t0003g0014a0002c0002t0004g0017 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-7-2501T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24592923 | ||||||
| chr1:24593028
|
A | G | 5 | a0001c0001t0001g0322a0001c0001t0001g0376a0001c0001t0001g0377others(2): Show | 5 | HG00639.hp2 HG01069.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-2396A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593028 | ||||||
| chr1:24593086
|
G | A | 93 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-7-2338G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593086 | ||||||
| chr1:24593115
|
T | C | 2 | a0001c0001t0006g0141a0001c0001t0026g0142 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-2309T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593115 | ||||||
| chr1:24593182
|
GA | G | 119 | a0001c0001t0001g0064a0001c0001t0001g0104a0001c0001t0001g0156others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-7-2229delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593182 | |||||
| chr1:24593244
|
G | A | 1 | a0001c0001t0008g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-2180G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593244 | ||||||
| chr1:24593266
|
T | C | 1 | a0001c0001t0005g0193 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-7-2158T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593266 | ||||||
| chr1:24593271
|
G | A | 1 | a0001c0001t0003g0368 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-7-2153G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593271 | ||||||
| chr1:24593321
|
TA | T | 298 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0055others(295): Show | 299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.-7-2093delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593321 | |||||
| chr1:24593455
|
T | C | 88 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(85): Show | 88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-7-1969T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593455 | ||||||
| chr1:24593627
|
T | A | 1 | a0001c0001t0001g0332 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-7-1797T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593627 | ||||||
| chr1:24593738
|
A | G | 2 | a0001c0001t0032g0317a0003c0003t0027g0276 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-1686A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593738 | ||||||
| chr1:24593786
|
G | T | 1 | a0001c0001t0002g0134 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-7-1638G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593786 | ||||||
| chr1:24593857
|
A | ATTAT | 7 | a0001c0001t0001g0122a0001c0001t0002g0115a0001c0001t0003g0070others(4): Show | 7 | HG00099.hp1 HG02148.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-1524_-7-1521dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | |||||
| chr1:24593857
|
ATTAT | A | 52 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0062others(49): Show | 53 | HG00140.hp2 HG00408.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.-7-1524_-7-1521del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | |||||
| chr1:24593857
|
ATTATTTA others(1): Show |
A | 173 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0078others(170): Show | 174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.-7-1528_-7-1521del others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | |||||
| chr1:24593857
|
ATTATTTA others(5): Show |
A | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-1532_-7-1521del others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | |||||
| chr1:24593857
|
ATTATTTA others(17): Show |
A | 12 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0006g0141others(9): Show | 12 | HG00558.hp1 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-1544_-7-1521del others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24593857 | |||||
| chr1:24593921
|
T | C | 1 | a0001c0001t0023g0071 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-7-1503T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24593921 | ||||||
| chr1:24594035
|
G | A | 76 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-7-1389G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594035 | ||||||
| chr1:24594038
|
CCCA | C | 108 | a0001c0001t0001g0104a0001c0001t0002g0021a0001c0001t0002g0026others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-7-1379_-7-1377del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24594038 | |||||
| chr1:24594107
|
G | A | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-1317G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594107 | ||||||
| chr1:24594126
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-7-1298A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594126 | ||||||
| chr1:24594227
|
G | C | 184 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.-7-1197G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594227 | ||||||
| chr1:24594248
|
A | C | 304 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0055others(301): Show | 305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.-7-1176A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594248 | ||||||
| chr1:24594343
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-7-1081G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594343 | ||||||
| chr1:24594490
|
C | A | 97 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-7-934C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594490 | ||||||
| chr1:24594555
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-7-869G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594555 | ||||||
| chr1:24594556
|
A | C | 3 | a0001c0001t0003g0392a0001c0001t0003g0394a0001c0001t0008g0150 | 3 | HG02572.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-868A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594556 | ||||||
| chr1:24594665
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-7-759T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594665 | ||||||
| chr1:24594778
|
T | A | 1 | a0001c0001t0001g0367 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-7-646T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594778 | ||||||
| chr1:24594842
|
GATTGCAC others(3): Show |
G | 1 | a0001c0001t0002g0095 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-7-581_-7-572delAT others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594842 | ||||||
| chr1:24594857
|
C | T | 108 | a0001c0001t0001g0104a0001c0001t0002g0021a0001c0001t0002g0026others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-7-567C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594857 | ||||||
| chr1:24594900
|
A | AT | 195 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0055others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-7-518dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24594900 | |||||
| chr1:24594900
|
A | T | 108 | a0001c0001t0001g0104a0001c0001t0002g0021a0001c0001t0002g0026others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-7-524A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594900 | ||||||
| chr1:24594975
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-7-449T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24594975 | ||||||
| chr1:24595038
|
GTTGA | G | 302 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0055others(299): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.-7-381_-7-378delTT others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 24595038 | |||||
| chr1:24595083
|
T | C | 4 | a0001c0001t0001g0400a0001c0001t0014g0397a0001c0001t0014g0398others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-341T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595083 | ||||||
| chr1:24595116
|
T | C | 1 | a0001c0001t0001g0337 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-7-308T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595116 | ||||||
| chr1:24595174
|
A | C | 2 | a0001c0001t0003g0392a0001c0001t0003g0394 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-250A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595174 | ||||||
| chr1:24595237
|
T | C | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-187T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595237 | ||||||
| chr1:24595241
|
G | A | 2 | a0001c0001t0002g0342a0001c0001t0002g0361 | 2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-7-183G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595241 | ||||||
| chr1:24595267
|
C | T | 85 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(82): Show | 85 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-7-157C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | chr1 | 24595267 | ||||||
| chr1:24595538
|
G | A | 1 | a0001c0001t0003g0385 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.82+26G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595538 | ||||||
| chr1:24595565
|
T | C | 77 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(74): Show | 77 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.82+53T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595565 | ||||||
| chr1:24595575
|
G | A | 1 | a0001c0001t0003g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82+63G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595575 | ||||||
| chr1:24595638
|
G | A | 182 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0055others(179): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.82+126G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595638 | ||||||
| chr1:24595675
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.82+163A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24595675 | ||||||
| chr1:24595794
|
C | CT | 61 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0078others(58): Show | 61 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.82+303dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | |||||
| chr1:24595794
|
C | CTTT | 9 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0006g0151others(6): Show | 9 | HG00558.hp1 HG01109.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.82+301_82+303dupTT others(1): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | |||||
| chr1:24595794
|
CT | C | 13 | a0001c0001t0001g0400a0001c0001t0002g0052a0001c0001t0002g0080others(10): Show | 13 | HG01106.hp1 HG01261.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.82+303delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | |||||
| chr1:24595794
|
CTTTT | C | 97 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0062others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.82+300_82+303delTT others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | |||||
| chr1:24595794
|
CTTTTT | C | 78 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0056others(75): Show | 78 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.82+299_82+303delTT others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595794 | |||||
| chr1:24595955
|
TA | T | 179 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0055others(176): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82+445delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24595955 | |||||
| chr1:24596156
|
C | T | 2 | a0001c0001t0008g0396a0002c0002t0004g0395 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.82+644C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596156 | ||||||
| chr1:24596528
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.82+1016C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596528 | ||||||
| chr1:24596579
|
G | C | 4 | a0001c0001t0003g0005a0001c0001t0003g0385a0002c0002t0004g0004others(1): Show | 4 | HG01106.hp1 HG02451.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+1067G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596579 | ||||||
| chr1:24596626
|
T | C | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.82+1114T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596626 | ||||||
| chr1:24596789
|
G | C | 7 | a0001c0001t0001g0323a0001c0001t0003g0010a0001c0001t0003g0011others(4): Show | 7 | HG01109.hp2 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+1277G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596789 | ||||||
| chr1:24596927
|
A | G | 3 | a0001c0001t0014g0397a0001c0001t0014g0398a0001c0001t0017g0399 | 3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+1415A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24596927 | ||||||
| chr1:24597063
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.82+1551G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597063 | ||||||
| chr1:24597124
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.82+1612G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597124 | ||||||
| chr1:24597313
|
C | T | 1 | a0001c0001t0001g0400 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.82+1801C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597313 | ||||||
| chr1:24597519
|
A | AG | 110 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0051others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.82+2018dupG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597519 | |||||
| chr1:24597519
|
AG | A | 29 | a0001c0001t0001g0061a0001c0001t0001g0298a0001c0001t0001g0300others(26): Show | 30 | HG00558.hp1 HG01123.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.82+2018delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597519 | |||||
| chr1:24597519
|
AGG | A | 89 | a0001c0001t0001g0104a0001c0001t0002g0026a0001c0001t0002g0027others(86): Show | 89 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.82+2017_82+2018del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597519 | |||||
| chr1:24597522
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.82+2010G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597522 | ||||||
| chr1:24597527
|
G | GA | 76 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0011others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.82+2015_82+2016ins others(1): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597527 | ||||||
| chr1:24597529
|
G | A | 7 | a0001c0001t0002g0095a0001c0001t0002g0113a0001c0001t0002g0115others(4): Show | 7 | HG00140.hp1 HG00544.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+2017G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597529 | ||||||
| chr1:24597530
|
GA | G | 7 | a0001c0001t0002g0047a0001c0001t0002g0095a0001c0001t0002g0113others(4): Show | 7 | HG00140.hp1 HG00544.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+2019delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597530 | ||||||
| chr1:24597531
|
A | G | 15 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0056others(12): Show | 15 | HG00621.hp2 HG01175.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.82+2019A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597531 | ||||||
| chr1:24597536
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82+2024G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597536 | ||||||
| chr1:24597537
|
A | AG | 11 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0158others(8): Show | 11 | HG00738.hp1 HG01433.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+2030dupG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597537 | |||||
| chr1:24597537
|
A | G | 2 | a0001c0001t0001g0311a0001c0001t0002g0271 | 2 | HG03942.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.82+2025A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597537 | ||||||
| chr1:24597546
|
G | A | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+2034G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597546 | ||||||
| chr1:24597555
|
A | AGGGAAGG others(10): Show |
16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2046_82+2047ins others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597555 | |||||
| chr1:24597580
|
C | A | 1 | a0001c0001t0002g0134 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.82+2068C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597580 | ||||||
| chr1:24597581
|
A | AAAAG | 125 | a0001c0001t0001g0104a0001c0001t0002g0021a0001c0001t0002g0026others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.82+2071_82+2074dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597581 | |||||
| chr1:24597581
|
A | G | 1 | a0001c0001t0002g0134 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.82+2069A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597581 | ||||||
| chr1:24597586
|
AG | A | 5 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0275others(2): Show | 6 | HG02723.hp2 HG02818.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2075delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597586 | ||||||
| chr1:24597587
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.82+2075G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597587 | ||||||
| chr1:24597590
|
GAA | G | 5 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0275others(2): Show | 6 | HG02723.hp2 HG02818.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2080_82+2081del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597590 | |||||
| chr1:24597593
|
A | AGAAGAAA others(35): Show |
4 | a0001c0001t0006g0190a0001c0001t0006g0280a0001c0001t0006g0284others(1): Show | 4 | HG00558.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2102_82+2103ins others(42): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597593 | |||||
| chr1:24597599
|
AAGAAAGA others(11): Show |
A | 16 | a0002c0002t0004g0016a0002c0002t0004g0017a0002c0002t0004g0023others(13): Show | 16 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2107_82+2124del others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597599 | |||||
| chr1:24597601
|
GAAAGAAA others(12): Show |
G | 5 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0275others(2): Show | 6 | HG02723.hp2 HG02818.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2092_82+2110del others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597601 | |||||
| chr1:24597603
|
A | AAGAAAGA others(11): Show |
1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+2102_82+2103ins others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597603 | |||||
| chr1:24597607
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0003g0077 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.82+2107_82+2116del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597607 | |||||
| chr1:24597613
|
GAAAGAGA others(1): Show |
G | 5 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0003g0014others(2): Show | 5 | HG02976.hp1 HG03225.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+2103_82+2110del others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597613 | |||||
| chr1:24597613
|
GAAAGAGA others(17): Show |
G | 1 | a0001c0001t0001g0156 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.82+2103_82+2126del others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597613 | |||||
| chr1:24597613
|
GAAAGAGA others(25): Show |
G | 2 | a0001c0001t0032g0317a0002c0002t0004g0395 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82+2103_82+2134del others(32): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597613 | |||||
| chr1:24597615
|
A | AAGAG | 26 | a0001c0001t0002g0040a0001c0001t0002g0044a0001c0001t0002g0068others(23): Show | 26 | HG00733.hp2 HG01167.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.82+2105_82+2108dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597615 | |||||
| chr1:24597615
|
A | AGAGAGAG others(6): Show |
1 | a0001c0001t0002g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.82+2103_82+2104ins others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597615 | ||||||
| chr1:24597615
|
A | G | 12 | a0001c0001t0003g0005a0001c0001t0006g0141a0001c0001t0006g0151others(9): Show | 12 | HG01106.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+2103A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597615 | ||||||
| chr1:24597617
|
G | A | 6 | a0001c0001t0002g0090a0001c0001t0003g0005a0001c0001t0006g0190others(3): Show | 6 | HG00558.hp1 HG01106.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2105G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597617 | ||||||
| chr1:24597617
|
G | C | 11 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2105G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597617 | ||||||
| chr1:24597617
|
G | GAAGAGAG others(4): Show |
1 | a0001c0001t0002g0292 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82+2106_82+2107ins others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
G | GAGAA | 52 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0001t0001g0051others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.82+2159_82+2162dup others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
G | GAGAAAGA others(1): Show |
29 | a0001c0001t0001g0078a0001c0001t0001g0114a0001c0001t0001g0125others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.82+2155_82+2162dup others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
G | GAGAAAGA others(5): Show |
10 | a0001c0001t0001g0110a0001c0001t0001g0191a0001c0001t0001g0227others(7): Show | 10 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+2151_82+2162dup others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
G | GAGAAAGA others(9): Show |
3 | a0001c0001t0001g0237a0001c0001t0003g0069a0001c0001t0003g0131 | 3 | HG04184.hp2 NA19081.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.82+2147_82+2162dup others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
G | GAGAGAGA others(1): Show |
18 | a0001c0001t0001g0104a0001c0001t0002g0043a0001c0001t0002g0113others(15): Show | 18 | HG00140.hp1 HG00423.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.82+2108_82+2109ins others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
G | GAGAGAGA others(5): Show |
5 | a0001c0001t0002g0021a0001c0001t0002g0042a0001c0001t0002g0081others(2): Show | 5 | HG03490.hp1 HG04184.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+2108_82+2109ins others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
G | GAGAGAGA others(9): Show |
2 | a0001c0001t0002g0052a0001c0001t0002g0094 | 2 | NA18960.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.82+2108_82+2109ins others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
G | GAGAGAGA others(13): Show |
1 | a0001c0001t0002g0157 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82+2108_82+2109ins others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
GAGAA | G | 33 | a0001c0001t0001g0137a0001c0001t0001g0158a0001c0001t0001g0161others(30): Show | 33 | HG00642.hp2 HG00733.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.82+2159_82+2162del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
GAGAAAGA others(1): Show |
G | 22 | a0001c0001t0001g0098a0001c0001t0001g0182a0001c0001t0001g0192others(19): Show | 22 | HG00639.hp2 HG01256.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.82+2155_82+2162del others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
GAGAAAGA others(5): Show |
G | 12 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0054others(9): Show | 12 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+2151_82+2162del others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
GAGAAAGA others(9): Show |
G | 7 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(4): Show | 7 | HG00438.hp2 HG00597.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+2147_82+2162del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
GAGAAAGA others(13): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.82+2143_82+2162del others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597617
|
GAGAAAGA others(17): Show |
G | 1 | a0001c0001t0011g0379 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.82+2139_82+2162del others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597617 | |||||
| chr1:24597619
|
G | A | 3 | a0001c0001t0014g0397a0001c0001t0014g0398a0001c0001t0017g0399 | 3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+2107G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597619 | ||||||
| chr1:24597621
|
A | C | 11 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2109A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597621 | ||||||
| chr1:24597621
|
A | G | 55 | a0001c0001t0001g0305a0001c0001t0002g0026a0001c0001t0002g0027others(52): Show | 55 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.82+2109A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597621 | ||||||
| chr1:24597633
|
A | AAG | 4 | a0001c0001t0006g0190a0001c0001t0006g0280a0001c0001t0006g0284others(1): Show | 4 | HG00558.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2123_82+2124dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597633 | |||||
| chr1:24597636
|
A | G | 11 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2124A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597636 | ||||||
| chr1:24597639
|
GAA | G | 21 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(18): Show | 22 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.82+2129_82+2130del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597639 | |||||
| chr1:24597640
|
AAAG | A | 3 | a0001c0001t0014g0397a0001c0001t0014g0398a0001c0001t0017g0399 | 3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+2131_82+2133del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597640 | |||||
| chr1:24597642
|
A | AGAAAGAA others(1): Show |
3 | a0001c0001t0001g0376a0001c0001t0001g0377a0001c0001t0001g0378 | 3 | HG01069.hp1 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.82+2137_82+2138ins others(8): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597642 | |||||
| chr1:24597644
|
A | G | 4 | a0001c0001t0006g0190a0001c0001t0006g0280a0001c0001t0006g0284others(1): Show | 4 | HG00558.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2132A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597644 | ||||||
| chr1:24597648
|
A | G | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+2136A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597648 | ||||||
| chr1:24597649
|
AAG | A | 3 | a0001c0001t0014g0397a0001c0001t0014g0398a0001c0001t0017g0399 | 3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+2139_82+2140del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597649 | |||||
| chr1:24597655
|
G | GAA | 11 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2145_82+2146dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597655 | |||||
| chr1:24597663
|
G | GAAAAGAA | 3 | a0001c0001t0002g0027a0001c0001t0002g0091a0001c0001t0002g0363 | 3 | HG00280.hp2 HG00621.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.82+2154_82+2155ins others(7): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597663 | |||||
| chr1:24597663
|
GAAAGAAA others(4): Show |
G | 1 | a0001c0001t0001g0203 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.82+2153_82+2163del others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597663 | |||||
| chr1:24597669
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.82+2157A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597669 | ||||||
| chr1:24597671
|
G | A | 11 | a0001c0001t0002g0026a0001c0001t0002g0080a0001c0001t0002g0119others(8): Show | 11 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+2159G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597671 | ||||||
| chr1:24597671
|
GAAAAGAA others(2): Show |
G | 3 | a0001c0001t0014g0397a0001c0001t0014g0398a0001c0001t0017g0399 | 3 | HG02055.hp1 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.82+2161_82+2169del others(9): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597671 | |||||
| chr1:24597672
|
A | AAAG | 8 | a0001c0001t0002g0027a0001c0001t0002g0091a0001c0001t0002g0363others(5): Show | 8 | HG00280.hp2 HG00558.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2162_82+2163ins others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597672 | |||||
| chr1:24597672
|
A | AAAGAAAG others(4): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0111 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.82+2162_82+2163ins others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597672 | |||||
| chr1:24597672
|
A | G | 11 | a0001c0001t0002g0026a0001c0001t0002g0080a0001c0001t0002g0119others(8): Show | 11 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+2160A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597672 | ||||||
| chr1:24597674
|
A | AG | 13 | a0001c0001t0001g0260a0001c0001t0006g0141a0001c0001t0006g0151others(10): Show | 13 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.82+2162_82+2163ins others(1): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597674 | ||||||
| chr1:24597676
|
G | A | 12 | a0001c0001t0002g0026a0001c0001t0002g0080a0001c0001t0002g0119others(9): Show | 12 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+2164G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597676 | ||||||
| chr1:24597678
|
A | AAG | 4 | a0001c0001t0006g0280a0001c0001t0006g0284a0001c0001t0006g0316others(1): Show | 4 | HG00558.hp1 HG03041.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2167_82+2168ins others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597678 | |||||
| chr1:24597678
|
A | AAGAAAGG others(23): Show |
3 | a0001c0001t0006g0290a0001c0001t0006g0366a0001c0001t0006g0386 | 3 | HG02896.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.82+2167_82+2168ins others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597678 | |||||
| chr1:24597678
|
A | AAGAAAGG others(27): Show |
7 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(4): Show | 7 | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+2167_82+2168ins others(34): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597678 | |||||
| chr1:24597678
|
A | AAGAAAGG others(30): Show |
1 | a0001c0001t0006g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.82+2167_82+2168ins others(37): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597678 | |||||
| chr1:24597678
|
A | G | 12 | a0001c0001t0002g0026a0001c0001t0002g0080a0001c0001t0002g0119others(9): Show | 12 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.82+2166A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597678 | ||||||
| chr1:24597680
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0091a0001c0001t0002g0363 | 3 | HG00280.hp2 HG00621.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.82+2168A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597680 | ||||||
| chr1:24597689
|
A | G | 6 | a0001c0001t0002g0027a0001c0001t0002g0091a0001c0001t0002g0363others(3): Show | 6 | HG00280.hp2 HG00621.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+2177A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597689 | ||||||
| chr1:24597692
|
AAG | A | 6 | a0001c0001t0002g0027a0001c0001t0002g0091a0001c0001t0002g0363others(3): Show | 6 | HG00280.hp2 HG00621.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+2184_82+2185del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597692 | |||||
| chr1:24597694
|
G | GAA | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2183_82+2184ins others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597694 | |||||
| chr1:24597694
|
G | GAAAGAGA others(9): Show |
93 | a0001c0001t0001g0104a0001c0001t0002g0021a0001c0001t0002g0035others(90): Show | 93 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.82+2183_82+2184ins others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597694 | |||||
| chr1:24597694
|
G | GAGAAAGA others(5): Show |
11 | a0001c0001t0002g0026a0001c0001t0002g0080a0001c0001t0002g0119others(8): Show | 11 | HG00735.hp2 HG01261.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+2186_82+2197dup others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24597694 | |||||
| chr1:24597703
|
G | A | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2191G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597703 | ||||||
| chr1:24597732
|
T | C | 2 | a0001c0001t0003g0147a0001c0001t0003g0277 | 2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.82+2220T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597732 | ||||||
| chr1:24597742
|
G | C | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2230G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597742 | ||||||
| chr1:24597745
|
A | C | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2233A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597745 | ||||||
| chr1:24597818
|
A | G | 3 | a0001c0001t0011g0273a0001c0001t0011g0379a0001c0001t0011g0380 | 3 | HG01891.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.82+2306A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597818 | ||||||
| chr1:24597820
|
C | A | 245 | a0001c0001t0001g0104a0001c0001t0001g0200a0001c0001t0002g0021others(242): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.82+2308C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597820 | ||||||
| chr1:24597878
|
T | C | 1 | a0001c0001t0008g0396 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82+2366T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597878 | ||||||
| chr1:24597970
|
G | C | 1 | a0001c0001t0005g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.82+2458G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597970 | ||||||
| chr1:24597989
|
A | G | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2477A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24597989 | ||||||
| chr1:24598001
|
T | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0286 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.82+2489T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598001 | ||||||
| chr1:24598038
|
T | C | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2526T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598038 | ||||||
| chr1:24598101
|
A | G | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2589A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598101 | ||||||
| chr1:24598210
|
C | T | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2698C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598210 | ||||||
| chr1:24598225
|
A | C | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.82+2713A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598225 | ||||||
| chr1:24598287
|
TG | T | 79 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0011others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.83-2650delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24598287 | |||||
| chr1:24598319
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.83-2621G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598319 | ||||||
| chr1:24598403
|
C | T | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-2537C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598403 | ||||||
| chr1:24598404
|
C | A | 1 | a0001c0001t0001g0337 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.83-2536C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598404 | ||||||
| chr1:24598405
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.83-2535C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598405 | ||||||
| chr1:24598440
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.83-2500C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598440 | ||||||
| chr1:24598446
|
G | A | 8 | a0001c0001t0001g0310a0001c0001t0007g0297a0001c0001t0007g0303others(5): Show | 8 | NA18947.hp2 NA18951.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-2494G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598446 | ||||||
| chr1:24598630
|
C | CT | 20 | a0001c0001t0001g0324a0001c0001t0006g0141a0001c0001t0006g0151others(17): Show | 20 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.83-2300dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24598630 | |||||
| chr1:24598826
|
C | T | 1 | a0001c0001t0003g0338 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.83-2114C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598826 | ||||||
| chr1:24598918
|
G | A | 5 | a0001c0001t0008g0001a0001c0001t0008g0018a0001c0001t0008g0019others(2): Show | 6 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2022G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598918 | ||||||
| chr1:24598928
|
A | G | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-2012A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598928 | ||||||
| chr1:24598950
|
T | C | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1990T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598950 | ||||||
| chr1:24598973
|
T | C | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1967T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24598973 | ||||||
| chr1:24599002
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0331 | 2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.83-1938G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599002 | ||||||
| chr1:24599108
|
C | T | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1832C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599108 | ||||||
| chr1:24599228
|
T | G | 1 | a0001c0001t0005g0176 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.83-1712T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599228 | ||||||
| chr1:24599240
|
A | G | 5 | a0001c0001t0008g0001a0001c0001t0008g0018a0001c0001t0008g0019others(2): Show | 6 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1700A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599240 | ||||||
| chr1:24599280
|
C | CA | 139 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0066others(136): Show | 139 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.83-1642dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599280 | |||||
| chr1:24599280
|
C | CAA | 6 | a0001c0001t0002g0021a0001c0001t0002g0045a0001c0001t0002g0134others(3): Show | 6 | HG01928.hp2 HG02486.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1643_83-1642dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599280 | |||||
| chr1:24599280
|
CA | C | 77 | a0001c0001t0001g0208a0001c0001t0001g0286a0001c0001t0001g0367others(74): Show | 77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.83-1642delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599280 | |||||
| chr1:24599342
|
C | T | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1598C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599342 | ||||||
| chr1:24599377
|
C | A | 111 | a0001c0001t0001g0104a0001c0001t0002g0021a0001c0001t0002g0026others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.83-1563C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599377 | ||||||
| chr1:24599391
|
C | G | 6 | a0001c0001t0002g0021a0001c0001t0002g0036a0001c0001t0002g0040others(3): Show | 6 | NA18954.hp1 NA18971.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1549C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599391 | ||||||
| chr1:24599420
|
A | AAAC | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1518_83-1516dup others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599420 | |||||
| chr1:24599488
|
C | T | 1 | a0001c0001t0030g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.83-1452C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599488 | ||||||
| chr1:24599553
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.83-1387A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599553 | ||||||
| chr1:24599618
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.83-1322C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599618 | ||||||
| chr1:24599703
|
G | C | 1 | a0001c0001t0002g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.83-1237G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599703 | ||||||
| chr1:24599724
|
C | G | 1 | a0001c0001t0001g0209 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.83-1216C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599724 | ||||||
| chr1:24599725
|
A | G | 291 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0037others(288): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.83-1215A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599725 | ||||||
| chr1:24599736
|
C | A | 1 | a0001c0001t0002g0075 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.83-1204C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599736 | ||||||
| chr1:24599775
|
C | A | 127 | a0001c0001t0001g0104a0001c0001t0002g0021a0001c0001t0002g0026others(124): Show | 127 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.83-1165C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599775 | ||||||
| chr1:24599818
|
C | T | 3 | a0001c0001t0006g0141a0001c0001t0006g0278a0001c0001t0026g0142 | 3 | HG01255.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.83-1122C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599818 | ||||||
| chr1:24599819
|
GC | G | 19 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0114others(16): Show | 19 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-1101delC | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | |||||
| chr1:24599819
|
GCC | G | 26 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0098others(23): Show | 26 | HG00323.hp2 HG01074.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.83-1102_83-1101del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | |||||
| chr1:24599819
|
GCCC | G | 55 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0061others(52): Show | 55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.83-1103_83-1101del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | |||||
| chr1:24599819
|
GCCCC | G | 87 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0058others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-1104_83-1101del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | |||||
| chr1:24599819
|
GCCCCC | G | 39 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0055others(36): Show | 39 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.83-1105_83-1101del others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | |||||
| chr1:24599819
|
GCCCCCC | G | 19 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0160others(16): Show | 19 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.83-1106_83-1101del others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599819 | |||||
| chr1:24599825
|
C | T | 2 | a0001c0001t0006g0327a0001c0001t0006g0366 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.83-1115C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599825 | ||||||
| chr1:24599826
|
C | A | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1114C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599826 | ||||||
| chr1:24599829
|
C | A | 24 | a0001c0001t0003g0010a0001c0001t0003g0012a0001c0001t0003g0069others(21): Show | 24 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.83-1111C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599829 | ||||||
| chr1:24599830
|
C | A | 54 | a0001c0001t0003g0005a0001c0001t0003g0011a0001c0001t0003g0014others(51): Show | 54 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.83-1110C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599830 | ||||||
| chr1:24599832
|
C | A | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1108C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599832 | ||||||
| chr1:24599834
|
C | CCCCCCCC others(4): Show |
3 | a0001c0001t0002g0041a0001c0001t0002g0050a0001c0001t0002g0361 | 3 | HG00438.hp1 HG03239.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.83-1101_83-1100ins others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | |||||
| chr1:24599834
|
C | CCCCCCCC others(3): Show |
2 | a0001c0001t0002g0085a0001c0001t0002g0136 | 2 | HG00741.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.83-1101_83-1100ins others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | |||||
| chr1:24599834
|
C | CCCCCCCG | 21 | a0001c0001t0002g0027a0001c0001t0002g0040a0001c0001t0002g0045others(18): Show | 21 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.83-1101_83-1100ins others(7): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | |||||
| chr1:24599834
|
C | CCCCCCG | 27 | a0001c0001t0001g0104a0001c0001t0002g0035a0001c0001t0002g0036others(24): Show | 27 | HG00735.hp2 HG01192.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.83-1101_83-1100ins others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | |||||
| chr1:24599834
|
C | CCCCCG | 19 | a0001c0001t0002g0044a0001c0001t0002g0075a0001c0001t0002g0091others(16): Show | 19 | HG00544.hp1 HG01123.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.83-1102_83-1101ins others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | |||||
| chr1:24599834
|
C | CCCCG | 15 | a0001c0001t0002g0026a0001c0001t0002g0043a0001c0001t0002g0072others(12): Show | 15 | HG00423.hp2 HG01167.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.83-1103_83-1102ins others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599834 | |||||
| chr1:24599834
|
CCCCCCTT | C | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1105_83-1099del others(7): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599834 | ||||||
| chr1:24599837
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.83-1103C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599837 | ||||||
| chr1:24599889
|
C | T | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-1051C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599889 | ||||||
| chr1:24599956
|
G | C | 127 | a0001c0001t0001g0104a0001c0001t0002g0021a0001c0001t0002g0026others(124): Show | 127 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.83-984G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24599956 | ||||||
| chr1:24599997
|
A | AT | 106 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0027others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.83-934dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599997 | |||||
| chr1:24599997
|
AT | A | 24 | a0001c0001t0001g0064a0001c0001t0001g0309a0001c0001t0006g0141others(21): Show | 25 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.83-934delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 24599997 | |||||
| chr1:24600006
|
T | A | 2 | a0001c0001t0003g0359a0001c0001t0003g0388 | 2 | HG00735.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.83-934T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600006 | ||||||
| chr1:24600025
|
A | G | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-915A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600025 | ||||||
| chr1:24600309
|
C | A | 10 | a0002c0002t0004g0017a0002c0002t0004g0029a0002c0002t0004g0030others(7): Show | 10 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.83-631C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600309 | ||||||
| chr1:24600344
|
G | A | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-596G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600344 | ||||||
| chr1:24600381
|
T | A | 15 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(12): Show | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.83-559T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600381 | ||||||
| chr1:24600393
|
A | T | 1 | a0001c0001t0002g0246 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.83-547A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600393 | ||||||
| chr1:24600402
|
C | T | 78 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0011others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.83-538C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600402 | ||||||
| chr1:24600499
|
G | C | 149 | a0001c0001t0001g0128a0001c0001t0002g0021a0001c0001t0002g0026others(146): Show | 150 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.83-441G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600499 | ||||||
| chr1:24600510
|
G | T | 78 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0011others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.83-430G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600510 | ||||||
| chr1:24600512
|
T | C | 5 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02040.hp2 NA18944.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-428T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600512 | ||||||
| chr1:24600537
|
C | A | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-403C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600537 | ||||||
| chr1:24600543
|
C | T | 17 | a0001c0001t0001g0200a0001c0001t0008g0001a0001c0001t0008g0007others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.83-397C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600543 | ||||||
| chr1:24600551
|
T | G | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.83-389T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600551 | ||||||
| chr1:24600757
|
G | A | 1 | a0001c0001t0001g0400 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.83-183G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600757 | ||||||
| chr1:24600778
|
T | G | 1 | a0001c0001t0014g0397 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83-162T>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600778 | ||||||
| chr1:24600907
|
C | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0117a0001c0001t0002g0118others(1): Show | 4 | NA18972.hp1 NA18986.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-33C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | chr1 | 24600907 | ||||||
| chr1:24601070
|
T | C | 224 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0027others(221): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.167+46T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601070 | ||||||
| chr1:24601100
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+76G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601100 | ||||||
| chr1:24601101
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+77G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601101 | ||||||
| chr1:24601102
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+78G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601102 | ||||||
| chr1:24601104
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+80G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601104 | ||||||
| chr1:24601106
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+82C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601106 | ||||||
| chr1:24601107
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+83C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601107 | ||||||
| chr1:24601108
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+84G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601108 | ||||||
| chr1:24601110
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+86C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601110 | ||||||
| chr1:24601113
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+89G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601113 | ||||||
| chr1:24601115
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+91G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601115 | ||||||
| chr1:24601116
|
C | G | 1 | a0001c0001t0032g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.167+92C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601116 | ||||||
| chr1:24601116
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+92C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601116 | ||||||
| chr1:24601117
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+93C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601117 | ||||||
| chr1:24601119
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+95G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601119 | ||||||
| chr1:24601120
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+96G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601120 | ||||||
| chr1:24601121
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+97C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601121 | ||||||
| chr1:24601122
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+98A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601122 | ||||||
| chr1:24601123
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+99G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601123 | ||||||
| chr1:24601125
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+101A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601125 | ||||||
| chr1:24601127
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+103C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601127 | ||||||
| chr1:24601128
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+104C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601128 | ||||||
| chr1:24601129
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+105C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601129 | ||||||
| chr1:24601131
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+107C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601131 | ||||||
| chr1:24601132
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+108A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601132 | ||||||
| chr1:24601133
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+109G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601133 | ||||||
| chr1:24601134
|
C | A | 78 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0011others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.167+110C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601134 | ||||||
| chr1:24601134
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+110C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601134 | ||||||
| chr1:24601135
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+111C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601135 | ||||||
| chr1:24601139
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+115A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601139 | ||||||
| chr1:24601140
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+116G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601140 | ||||||
| chr1:24601142
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+118A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601142 | ||||||
| chr1:24601143
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+119A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601143 | ||||||
| chr1:24601144
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+120A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601144 | ||||||
| chr1:24601146
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+122G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601146 | ||||||
| chr1:24601147
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+123C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601147 | ||||||
| chr1:24601149
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+125C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601149 | ||||||
| chr1:24601151
|
A | C | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+127A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601151 | ||||||
| chr1:24601152
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+128A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601152 | ||||||
| chr1:24601153
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+129C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601153 | ||||||
| chr1:24601154
|
C | G | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+130C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601154 | ||||||
| chr1:24601155
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+131C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601155 | ||||||
| chr1:24601156
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+132T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601156 | ||||||
| chr1:24601159
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+135G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601159 | ||||||
| chr1:24601161
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+137G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601161 | ||||||
| chr1:24601162
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.167+138A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601162 | ||||||
| chr1:24601236
|
C | G | 10 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0106others(7): Show | 10 | HG00642.hp1 HG01099.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+212C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601236 | ||||||
| chr1:24601236
|
C | T | 126 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0027others(123): Show | 126 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.167+212C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601236 | ||||||
| chr1:24601240
|
G | A | 148 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0027others(145): Show | 149 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.167+216G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601240 | ||||||
| chr1:24601290
|
T | A | 1 | a0001c0001t0007g0079 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.167+266T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601290 | ||||||
| chr1:24601447
|
G | T | 1 | a0001c0001t0001g0400 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.167+423G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601447 | ||||||
| chr1:24601561
|
A | T | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+537A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601561 | ||||||
| chr1:24601627
|
C | T | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.167+603C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601627 | ||||||
| chr1:24601675
|
C | T | 1 | a0001c0001t0003g0333 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.167+651C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601675 | ||||||
| chr1:24601695
|
A | G | 1 | a0001c0001t0002g0068 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.167+671A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601695 | ||||||
| chr1:24601820
|
A | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+796A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601820 | ||||||
| chr1:24601830
|
G | A | 1 | a0001c0001t0003g0256 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.167+806G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601830 | ||||||
| chr1:24601856
|
T | C | 15 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(12): Show | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.167+832T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601856 | ||||||
| chr1:24601885
|
G | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+861G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601885 | ||||||
| chr1:24601906
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.167+882C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601906 | ||||||
| chr1:24601914
|
G | T | 1 | a0001c0001t0001g0337 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.167+890G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601914 | ||||||
| chr1:24601937
|
A | C | 17 | a0001c0001t0001g0200a0001c0001t0008g0001a0001c0001t0008g0007others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.167+913A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24601937 | ||||||
| chr1:24602030
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1006A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602030 | ||||||
| chr1:24602040
|
C | CA | 30 | a0001c0001t0001g0063a0001c0001t0001g0125a0001c0001t0001g0186others(27): Show | 31 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.167+1030dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602040 | |||||
| chr1:24602040
|
C | CAA | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1029_167+1030d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602040 | |||||
| chr1:24602040
|
CA | C | 196 | a0001c0001t0001g0066a0001c0001t0001g0314a0001c0001t0002g0021others(193): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.167+1030delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602040 | |||||
| chr1:24602104
|
C | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1080C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602104 | ||||||
| chr1:24602154
|
C | T | 6 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0275others(3): Show | 7 | HG01891.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.167+1130C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602154 | ||||||
| chr1:24602202
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1178A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602202 | ||||||
| chr1:24602230
|
G | A | 8 | a0001c0001t0002g0086a0001c0001t0002g0095a0001c0001t0002g0173others(5): Show | 8 | HG00423.hp2 HG02080.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+1206G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602230 | ||||||
| chr1:24602304
|
TAAGAATA others(279): Show |
T | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1298_167+1583d others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602304 | |||||
| chr1:24602357
|
C | A | 1 | a0001c0001t0030g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.167+1333C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602357 | ||||||
| chr1:24602426
|
C | G | 1 | a0001c0001t0005g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.167+1402C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602426 | ||||||
| chr1:24602427
|
G | C | 1 | a0001c0001t0005g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.167+1403G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602427 | ||||||
| chr1:24602438
|
T | C | 204 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0027others(201): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.167+1414T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602438 | ||||||
| chr1:24602497
|
A | G | 107 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0027others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.167+1473A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602497 | ||||||
| chr1:24602546
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.167+1522G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602546 | ||||||
| chr1:24602565
|
A | G | 19 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(16): Show | 19 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.167+1541A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602565 | ||||||
| chr1:24602569
|
C | CA | 20 | a0001c0001t0001g0156a0001c0001t0001g0221a0001c0001t0001g0235others(17): Show | 20 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.167+1568dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | |||||
| chr1:24602569
|
C | CAA | 86 | a0001c0001t0001g0200a0001c0001t0002g0086a0001c0001t0002g0138others(83): Show | 87 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.167+1567_167+1568d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | |||||
| chr1:24602569
|
C | CAAA | 104 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0027others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.167+1566_167+1568d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | |||||
| chr1:24602569
|
C | CAAAA | 18 | a0001c0001t0002g0041a0001c0001t0002g0068a0001c0001t0002g0095others(15): Show | 18 | HG00140.hp1 HG00544.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.167+1565_167+1568d others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | |||||
| chr1:24602569
|
CA | C | 12 | a0001c0001t0001g0098a0001c0001t0001g0105a0001c0001t0001g0137others(9): Show | 12 | HG01069.hp1 HG01074.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.167+1568delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602569 | |||||
| chr1:24602738
|
G | GA | 16 | a0001c0001t0002g0113a0001c0001t0003g0089a0002c0002t0004g0004others(13): Show | 17 | HG00140.hp1 HG01099.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+1726dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602738 | |||||
| chr1:24602738
|
GA | G | 17 | a0001c0001t0001g0324a0001c0001t0006g0141a0001c0001t0006g0151others(14): Show | 17 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+1726delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24602738 | |||||
| chr1:24602781
|
G | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1757G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602781 | ||||||
| chr1:24602794
|
C | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1770C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602794 | ||||||
| chr1:24602802
|
C | T | 1 | a0001c0001t0003g0352 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.167+1778C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602802 | ||||||
| chr1:24602872
|
C | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+1848C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602872 | ||||||
| chr1:24602971
|
C | T | 3 | a0001c0001t0003g0005a0001c0001t0003g0345a0001c0001t0003g0387 | 3 | HG01106.hp1 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.167+1947C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24602971 | ||||||
| chr1:24603059
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.167+2035A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603059 | ||||||
| chr1:24603102
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2078T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603102 | ||||||
| chr1:24603152
|
T | C | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.167+2128T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603152 | ||||||
| chr1:24603185
|
G | A | 245 | a0001c0001t0001g0200a0001c0001t0002g0021a0001c0001t0002g0026others(242): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.167+2161G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603185 | ||||||
| chr1:24603210
|
A | AT | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.167+2190dupT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24603210 | |||||
| chr1:24603222
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2198T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603222 | ||||||
| chr1:24603231
|
A | G | 3 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0275 | 3 | HG02818.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.167+2207A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603231 | ||||||
| chr1:24603252
|
T | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2228T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603252 | ||||||
| chr1:24603275
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2251T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603275 | ||||||
| chr1:24603283
|
G | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.167+2259G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603283 | ||||||
| chr1:24603337
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2269A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603337 | ||||||
| chr1:24603339
|
GTAA | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2254_168-2252d others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24603339 | |||||
| chr1:24603353
|
A | T | 1 | a0001c0001t0029g0362 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.168-2253A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603353 | ||||||
| chr1:24603364
|
A | G | 246 | a0001c0001t0001g0200a0001c0001t0002g0021a0001c0001t0002g0026others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.168-2242A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603364 | ||||||
| chr1:24603378
|
A | AG | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2228_168-2227i others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603378 | ||||||
| chr1:24603434
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2172A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603434 | ||||||
| chr1:24603488
|
G | A | 1 | a0001c0001t0003g0351 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.168-2118G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603488 | ||||||
| chr1:24603533
|
C | T | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-2073C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603533 | ||||||
| chr1:24603623
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1983A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603623 | ||||||
| chr1:24603695
|
G | T | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168-1911G>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603695 | ||||||
| chr1:24603751
|
C | T | 1 | a0002c0002t0004g0395 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-1855C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603751 | ||||||
| chr1:24603752
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1854A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603752 | ||||||
| chr1:24603802
|
A | AG | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1803dupG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24603802 | |||||
| chr1:24603869
|
T | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1737T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24603869 | ||||||
| chr1:24604044
|
A | G | 2 | a0002c0002t0013g0002a0002c0002t0013g0146 | 3 | HG02723.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.168-1562A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604044 | ||||||
| chr1:24604145
|
G | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1461G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604145 | ||||||
| chr1:24604152
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.168-1454A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604152 | ||||||
| chr1:24604188
|
CT | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1412delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604188 | |||||
| chr1:24604267
|
T | C | 15 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(12): Show | 15 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-1339T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604267 | ||||||
| chr1:24604272
|
A | T | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1334A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604272 | ||||||
| chr1:24604282
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1324A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604282 | ||||||
| chr1:24604325
|
G | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1281G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604325 | ||||||
| chr1:24604353
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1253T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604353 | ||||||
| chr1:24604417
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1189A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604417 | ||||||
| chr1:24604439
|
G | C | 1 | a0001c0001t0002g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.168-1167G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604439 | ||||||
| chr1:24604462
|
C | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1144C>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604462 | ||||||
| chr1:24604463
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1143T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604463 | ||||||
| chr1:24604559
|
AG | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1044delG | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604559 | |||||
| chr1:24604563
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.168-1043T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604563 | ||||||
| chr1:24604567
|
A | ACT | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-1038_168-1037d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604567 | |||||
| chr1:24604573
|
T | TA | 9 | a0001c0001t0001g0055a0001c0001t0001g0158a0001c0001t0001g0160others(6): Show | 9 | HG00597.hp1 HG01257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1000dupA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
T | TAA | 8 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0122others(5): Show | 8 | HG00280.hp2 HG01168.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-1001_168-1000d others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TA | T | 9 | a0001c0001t0001g0203a0001c0001t0001g0260a0001c0001t0001g0299others(6): Show | 9 | HG01975.hp1 NA18612.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.168-1000delA | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0006g0278a0002c0002t0004g0389 | 2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.168-1011_168-1000d others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(7): Show |
T | 1 | a0002c0002t0004g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168-1013_168-1000d others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(9): Show |
T | 2 | a0002c0002t0004g0016a0002c0002t0004g0017 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.168-1015_168-1000d others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(11): Show |
T | 4 | a0002c0002t0004g0006a0002c0002t0004g0023a0002c0002t0004g0201others(1): Show | 4 | HG02572.hp1 HG02809.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1017_168-1000d others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(12): Show |
T | 1 | a0002c0002t0013g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-1018_168-1000d others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(13): Show |
T | 7 | a0002c0002t0004g0025a0002c0002t0004g0029a0002c0002t0004g0033others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-1019_168-1000d others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(14): Show |
T | 1 | a0002c0002t0013g0002 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.168-1020_168-1000d others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(15): Show |
T | 3 | a0002c0002t0004g0030a0002c0002t0004g0031a0002c0002t0004g0057 | 3 | HG02647.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-1021_168-1000d others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604573
|
TAAAAAAA others(21): Show |
T | 1 | a0002c0002t0004g0395 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-1027_168-1000d others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604573 | |||||
| chr1:24604574
|
A | C | 1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1032A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604574 | ||||||
| chr1:24604579
|
A | T | 1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1027A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604579 | ||||||
| chr1:24604581
|
A | T | 1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1025A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604581 | ||||||
| chr1:24604583
|
A | T | 1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1023A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604583 | ||||||
| chr1:24604585
|
A | T | 1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1021A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604585 | ||||||
| chr1:24604586
|
A | C | 1 | a0002c0002t0004g0389 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.168-1020A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604586 | ||||||
| chr1:24604586
|
AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0006g0152a0001c0001t0006g0153 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.168-1018_168-994de others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604586 | |||||
| chr1:24604587
|
A | T | 1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1019A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604587 | ||||||
| chr1:24604588
|
A | C | 1 | a0002c0002t0004g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168-1018A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604588 | ||||||
| chr1:24604589
|
A | T | 1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-1017A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604589 | ||||||
| chr1:24604589
|
AAAAAAAA others(17): Show |
A | 2 | a0001c0001t0006g0141a0001c0001t0026g0142 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.168-1015_168-992de others(25): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604589 | |||||
| chr1:24604590
|
A | C | 2 | a0002c0002t0004g0016a0002c0002t0004g0017 | 2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.168-1016A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604590 | ||||||
| chr1:24604591
|
A | T | 2 | a0002c0002t0004g0004a0002c0002t0004g0389 | 2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.168-1015A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604591 | ||||||
| chr1:24604591
|
AAAAAAAA others(27): Show |
A | 1 | a0001c0001t0003g0010 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.168-1013_168-980de others(35): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604591 | |||||
| chr1:24604592
|
A | C | 4 | a0002c0002t0004g0006a0002c0002t0004g0023a0002c0002t0004g0201others(1): Show | 4 | HG02572.hp1 HG02809.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1014A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604592 | ||||||
| chr1:24604592
|
AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0006g0290a0001c0001t0006g0316 | 2 | HG03130.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.168-1012_168-998de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604592 | |||||
| chr1:24604592
|
AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0006g0287a0001c0001t0006g0386 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.168-1012_168-996de others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604592 | |||||
| chr1:24604592
|
AAAAAAAA others(12): Show |
A | 2 | a0001c0001t0006g0151a0001c0001t0006g0284 | 2 | HG00558.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.168-1012_168-994de others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604592 | |||||
| chr1:24604593
|
A | C | 1 | a0002c0002t0013g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-1013A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604593 | ||||||
| chr1:24604593
|
A | T | 3 | a0002c0002t0004g0004a0002c0002t0004g0275a0002c0002t0004g0389 | 3 | HG01099.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.168-1013A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604593 | ||||||
| chr1:24604594
|
A | C | 7 | a0002c0002t0004g0025a0002c0002t0004g0029a0002c0002t0004g0033others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-1012A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604594 | ||||||
| chr1:24604594
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0008g0396 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.168-1010_168-982de others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604594 | |||||
| chr1:24604595
|
A | C | 1 | a0002c0002t0013g0002 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.168-1011A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604595 | ||||||
| chr1:24604595
|
A | T | 5 | a0002c0002t0004g0004a0002c0002t0004g0016a0002c0002t0004g0017others(2): Show | 5 | HG01099.hp2 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-1011A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604595 | ||||||
| chr1:24604595
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0367 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.168-1009_168-998de others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604595 | |||||
| chr1:24604595
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0006g0280 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.168-1009_168-996de others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604595 | |||||
| chr1:24604595
|
AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0058a0001c0001t0032g0317 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.168-1009_168-992de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604595 | |||||
| chr1:24604595
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0006g0190 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.168-1009_168-990de others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604595 | |||||
| chr1:24604596
|
A | C | 3 | a0002c0002t0004g0030a0002c0002t0004g0031a0002c0002t0004g0057 | 3 | HG02647.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.168-1010A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604596 | ||||||
| chr1:24604596
|
AAAAAAAA others(8): Show |
A | 1 | a0003c0003t0027g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168-1008_168-994de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604596 | |||||
| chr1:24604596
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0003g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.168-1008_168-986de others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604596 | |||||
| chr1:24604596
|
AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0011g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.168-1008_168-982de others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604596 | |||||
| chr1:24604596
|
AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0015g0008a0001c0001t0015g0009 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.168-1008_168-980de others(30): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604596 | |||||
| chr1:24604597
|
A | T | 9 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(6): Show | 9 | HG01099.hp2 HG01243.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1009A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604597 | ||||||
| chr1:24604597
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0006g0366 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.168-1007_168-994de others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604597 | |||||
| chr1:24604597
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0003g0373 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.168-1007_168-992de others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604597 | |||||
| chr1:24604597
|
AAAAAAAA others(11): Show |
A | 3 | a0001c0001t0001g0323a0001c0001t0003g0374a0001c0001t0006g0327 | 3 | HG02080.hp2 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.168-1007_168-990de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604597 | |||||
| chr1:24604598
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0003g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.168-1006_168-992de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | |||||
| chr1:24604598
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0003g0385 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.168-1006_168-990de others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | |||||
| chr1:24604598
|
AAAAAAAA others(16): Show |
A | 2 | a0001c0001t0003g0053a0001c0001t0003g0147 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.168-1006_168-984de others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | |||||
| chr1:24604598
|
AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0011g0379a0001c0001t0011g0380 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.168-1006_168-982de others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | |||||
| chr1:24604598
|
AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0008g0018 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.168-1006_168-980de others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604598 | |||||
| chr1:24604599
|
A | T | 16 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(13): Show | 16 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.168-1007A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604599 | ||||||
| chr1:24604599
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0377a0001c0001t0001g0378a0001c0001t0010g0059 | 3 | HG01069.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.168-1005_168-994de others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | |||||
| chr1:24604599
|
AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0002g0043a0001c0001t0014g0398a0001c0001t0017g0399 | 3 | HG02055.hp1 HG02486.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.168-1005_168-990de others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | |||||
| chr1:24604599
|
AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0054a0001c0001t0003g0244 | 2 | HG00140.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.168-1005_168-988de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | |||||
| chr1:24604599
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0018g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.168-1005_168-986de others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | |||||
| chr1:24604599
|
AAAAAAAA others(15): Show |
A | 2 | a0001c0001t0003g0277a0001c0001t0019g0347 | 2 | HG02027.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.168-1005_168-984de others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | |||||
| chr1:24604599
|
AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0012g0215 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.168-1005_168-980de others(27): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | |||||
| chr1:24604599
|
AAAAAAAA others(21): Show |
A | 4 | a0001c0001t0001g0200a0001c0001t0001g0220a0001c0001t0008g0007others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1005_168-978de others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604599 | |||||
| chr1:24604600
|
AAAAAAAT others(4): Show |
A | 2 | a0001c0001t0001g0322a0001c0001t0001g0376 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.168-1004_168-994de others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | |||||
| chr1:24604600
|
AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0001g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.168-1004_168-992de others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | |||||
| chr1:24604600
|
AAAAAAAT others(10): Show |
A | 4 | a0001c0001t0002g0094a0001c0001t0002g0252a0001c0001t0003g0225others(1): Show | 4 | HG00735.hp2 HG01361.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1004_168-988de others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | |||||
| chr1:24604600
|
AAAAAAAT others(12): Show |
A | 2 | a0001c0001t0003g0012a0001c0001t0003g0240 | 2 | HG02622.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.168-1004_168-986de others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | |||||
| chr1:24604600
|
AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0003g0070 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.168-1004_168-984de others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | |||||
| chr1:24604600
|
AAAAAAAT others(18): Show |
A | 2 | a0001c0001t0012g0154a0001c0001t0012g0202 | 2 | HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.168-1004_168-980de others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | |||||
| chr1:24604600
|
AAAAAAAT others(20): Show |
A | 4 | a0001c0001t0008g0001a0001c0001t0008g0019a0001c0001t0008g0022others(1): Show | 5 | HG02145.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-1004_168-978de others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604600 | |||||
| chr1:24604601
|
A | T | 19 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(16): Show | 19 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.168-1005A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604601 | ||||||
| chr1:24604601
|
AAAAAATA others(3): Show |
A | 2 | a0001c0001t0001g0155a0001c0001t0001g0192 | 2 | HG03130.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.168-1003_168-994de others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | |||||
| chr1:24604601
|
AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0144a0001c0001t0010g0060 | 2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.168-1003_168-992de others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | |||||
| chr1:24604601
|
AAAAAATA others(9): Show |
A | 1 | a0001c0001t0001g0051 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.168-1003_168-988de others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | |||||
| chr1:24604601
|
AAAAAATA others(11): Show |
A | 6 | a0001c0001t0003g0145a0001c0001t0003g0242a0001c0001t0003g0243others(3): Show | 6 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-1003_168-986de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | |||||
| chr1:24604601
|
AAAAAATA others(13): Show |
A | 2 | a0001c0001t0003g0015a0001c0001t0030g0003 | 2 | HG02922.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.168-1003_168-984de others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | |||||
| chr1:24604601
|
AAAAAATA others(19): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.168-1003_168-978de others(27): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | |||||
| chr1:24604601
|
AAAAAATA others(21): Show |
A | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.168-1003_168-976de others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604601 | |||||
| chr1:24604602
|
A | C | 1 | a0002c0002t0004g0395 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-1004A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604602 | ||||||
| chr1:24604602
|
AAAAATAT others(4): Show |
A | 1 | a0001c0001t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.168-1002_168-992de others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | |||||
| chr1:24604602
|
AAAAATAT others(6): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.168-1002_168-990de others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | |||||
| chr1:24604602
|
AAAAATAT others(8): Show |
A | 1 | a0001c0001t0014g0397 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.168-1002_168-988de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | |||||
| chr1:24604602
|
AAAAATAT others(10): Show |
A | 1 | a0001c0001t0003g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.168-1002_168-986de others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | |||||
| chr1:24604602
|
AAAAATAT others(12): Show |
A | 2 | a0001c0001t0003g0319a0001c0001t0003g0358 | 2 | HG01169.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.168-1002_168-984de others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | |||||
| chr1:24604602
|
AAAAATAT others(14): Show |
A | 2 | a0001c0001t0003g0077a0001c0001t0003g0345 | 2 | HG02717.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.168-1002_168-982de others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604602 | |||||
| chr1:24604603
|
A | T | 26 | a0001c0001t0002g0026a0001c0001t0002g0040a0001c0001t0002g0042others(23): Show | 26 | HG01099.hp2 HG01243.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.168-1003A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604603 | ||||||
| chr1:24604603
|
AAAATATA others(5): Show |
A | 4 | a0001c0001t0002g0027a0001c0001t0002g0279a0001c0001t0002g0295others(1): Show | 4 | HG00621.hp1 HG01167.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1001_168-990de others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | |||||
| chr1:24604603
|
AAAATATA others(11): Show |
A | 8 | a0001c0001t0002g0216a0001c0001t0003g0089a0001c0001t0003g0253others(5): Show | 8 | HG00323.hp1 HG01255.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.168-1001_168-984de others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | |||||
| chr1:24604603
|
AAAATATA others(13): Show |
A | 1 | a0001c0001t0003g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.168-1001_168-982de others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | |||||
| chr1:24604603
|
AAAATATA others(15): Show |
A | 9 | a0001c0001t0002g0218a0001c0001t0002g0247a0001c0001t0002g0344others(6): Show | 9 | HG02080.hp1 HG02559.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1001_168-980de others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | |||||
| chr1:24604603
|
AAAATATA others(17): Show |
A | 4 | a0001c0001t0001g0121a0001c0001t0001g0206a0001c0001t0003g0325others(1): Show | 4 | HG00558.hp2 HG02040.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1001_168-978de others(25): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | |||||
| chr1:24604603
|
AAAATATA others(19): Show |
A | 3 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0286 | 3 | HG01175.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.168-1001_168-976de others(27): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | |||||
| chr1:24604603
|
AAAATATA others(23): Show |
A | 1 | a0001c0001t0002g0294 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.168-1001_168-972de others(31): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | |||||
| chr1:24604603
|
AAAATATA others(29): Show |
A | 1 | a0001c0001t0002g0164 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.168-1001_168-966de others(37): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604603 | |||||
| chr1:24604604
|
AAATAT | A | 6 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0191others(3): Show | 6 | HG00642.hp2 HG01081.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-1000_168-996de others(6): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604604
|
AAATATAT others(2): Show |
A | 6 | a0001c0001t0001g0112a0001c0001t0002g0045a0001c0001t0002g0118others(3): Show | 6 | HG00673.hp2 NA18972.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-1000_168-992de others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604604
|
AAATATAT others(4): Show |
A | 1 | a0001c0001t0001g0289 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.168-1000_168-990de others(12): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604604
|
AAATATAT others(8): Show |
A | 1 | a0001c0001t0002g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.168-1000_168-986de others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604604
|
AAATATAT others(12): Show |
A | 3 | a0001c0001t0003g0069a0001c0001t0003g0219a0001c0001t0003g0320 | 3 | HG01167.hp1 HG04184.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.168-1000_168-982de others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604604
|
AAATATAT others(14): Show |
A | 9 | a0001c0001t0002g0248a0001c0001t0002g0343a0001c0001t0003g0005others(6): Show | 9 | HG00099.hp1 HG00423.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1000_168-980de others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604604
|
AAATATAT others(16): Show |
A | 2 | a0001c0001t0001g0049a0001c0001t0003g0226 | 2 | HG01361.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.168-1000_168-978de others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604604
|
AAATATAT others(18): Show |
A | 1 | a0001c0001t0001g0222 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.168-1000_168-976de others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604604
|
AAATATAT others(28): Show |
A | 1 | a0001c0001t0007g0180 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.168-1000_168-966de others(36): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604604 | |||||
| chr1:24604605
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.168-1000_168-999in others(13): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.168-1000_168-999in others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.168-1000_168-999in others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
A | AAAT | 7 | a0001c0001t0001g0028a0001c0001t0001g0259a0001c0001t0001g0262others(4): Show | 7 | HG02165.hp1 HG02615.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-1000_168-999in others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0007g0297 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.168-1000_168-999in others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
A | AAT | 7 | a0001c0001t0001g0078a0001c0001t0001g0107a0001c0001t0001g0239others(4): Show | 7 | HG00099.hp2 HG02027.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-954_168-953dup others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
A | ATAT | 4 | a0001c0001t0001g0161a0001c0001t0001g0314a0001c0001t0001g0324others(1): Show | 4 | NA18946.hp2 NA18948.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1001_168-1000i others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604605 | ||||||
| chr1:24604605
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0007g0307 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.168-1001_168-1000i others(15): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604605 | ||||||
| chr1:24604605
|
A | T | 33 | a0001c0001t0001g0127a0001c0001t0001g0140a0001c0001t0001g0227others(30): Show | 33 | HG01099.hp2 HG01243.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.168-1001A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604605 | ||||||
| chr1:24604605
|
AAT | A | 9 | a0001c0001t0001g0214a0001c0001t0001g0223a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp2 HG00733.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-954_168-953del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATAT | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0169a0001c0001t0001g0182others(9): Show | 12 | HG00621.hp2 HG00673.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.168-956_168-953del others(4): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0001g0282 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.168-962_168-953del others(10): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(7): Show |
A | 1 | a0001c0001t0001g0265 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.168-966_168-953del others(14): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(9): Show |
A | 3 | a0001c0001t0001g0106a0001c0001t0003g0074a0001c0001t0003g0092 | 3 | HG02300.hp1 HG04115.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.168-968_168-953del others(16): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(11): Show |
A | 5 | a0001c0001t0001g0183a0001c0001t0002g0361a0001c0001t0003g0076others(2): Show | 5 | HG03239.hp2 NA18940.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-970_168-953del others(18): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(13): Show |
A | 5 | a0001c0001t0003g0354a0001c0001t0003g0355a0001c0001t0003g0356others(2): Show | 5 | HG01074.hp2 HG01516.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-972_168-953del others(20): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0003g0365 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.168-974_168-953del others(22): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(17): Show |
A | 2 | a0001c0001t0003g0011a0001c0001t0003g0372 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168-976_168-953del others(24): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(19): Show |
A | 3 | a0001c0001t0001g0228a0001c0001t0001g0261a0001c0001t0001g0270 | 3 | HG01261.hp1 HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.168-978_168-953del others(26): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(27): Show |
A | 1 | a0001c0001t0002g0068 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.168-986_168-953del others(34): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604605
|
AATATATA others(29): Show |
A | 1 | a0001c0001t0002g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.168-988_168-953del others(36): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604605 | |||||
| chr1:24604606
|
AT | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0230a0001c0001t0002g0342others(2): Show | 5 | HG01358.hp2 HG02040.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-999delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604606
|
ATAT | A | 12 | a0001c0001t0001g0181a0001c0001t0001g0186a0001c0001t0001g0204others(9): Show | 12 | HG00280.hp1 HG01943.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.168-999_168-997del others(3): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604606
|
ATATAT | A | 6 | a0001c0001t0001g0208a0001c0001t0002g0075a0001c0001t0002g0090others(3): Show | 6 | HG01123.hp2 HG04184.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-999_168-995del others(5): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604606
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.168-999_168-989del others(11): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604606
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0003g0360 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.168-999_168-983del others(17): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604606
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0003g0256a0001c0001t0003g0371 | 2 | HG00544.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.168-999_168-981del others(19): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604606
|
ATATATAT others(14): Show |
A | 6 | a0001c0001t0002g0116a0001c0001t0003g0131a0001c0001t0003g0132others(3): Show | 6 | HG02155.hp2 NA18952.hp2 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-999_168-979del others(21): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604606
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0016g0341 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.168-999_168-977del others(23): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604606
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0283 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168-999_168-969del others(31): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604606 | ||||||
| chr1:24604607
|
T | A | 19 | a0001c0001t0001g0055a0001c0001t0001g0098a0001c0001t0001g0114others(16): Show | 19 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.168-999T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604607 | ||||||
| chr1:24604609
|
T | A | 14 | a0001c0001t0001g0114a0001c0001t0001g0139a0001c0001t0001g0210others(11): Show | 14 | HG00597.hp1 HG00597.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.168-997T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604609 | ||||||
| chr1:24604611
|
T | A | 10 | a0001c0001t0001g0204a0001c0001t0001g0214a0001c0001t0001g0298others(7): Show | 10 | HG00597.hp2 HG01928.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.168-995T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604611 | ||||||
| chr1:24604613
|
T | A | 7 | a0001c0001t0001g0204a0001c0001t0001g0214a0001c0001t0001g0224others(4): Show | 7 | HG01123.hp2 HG02074.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-993T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604613 | ||||||
| chr1:24604615
|
T | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0382a0001c0001t0002g0075 | 3 | HG00639.hp2 HG01123.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.168-991T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604615 | ||||||
| chr1:24604617
|
T | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0382 | 2 | HG00639.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.168-989T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604617 | ||||||
| chr1:24604623
|
T | A | 2 | a0001c0001t0001g0106a0001c0001t0003g0092 | 2 | HG02300.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.168-983T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604623 | ||||||
| chr1:24604625
|
T | A | 3 | a0001c0001t0001g0106a0001c0001t0003g0339a0001c0001t0005g0336 | 3 | HG02300.hp1 NA18998.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.168-981T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604625 | ||||||
| chr1:24604627
|
T | A | 2 | a0001c0001t0003g0339a0001c0001t0003g0354 | 2 | HG01516.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.168-979T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604627 | ||||||
| chr1:24604628
|
A | ATGTGTGT others(41): Show |
1 | a0002c0002t0004g0395 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-977_168-976ins others(48): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604628 | |||||
| chr1:24604629
|
T | A | 1 | a0001c0001t0003g0339 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.168-977T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604629 | ||||||
| chr1:24604630
|
A | ATGTGTGT others(27): Show |
1 | a0002c0002t0013g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-975_168-974ins others(34): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604630 | |||||
| chr1:24604630
|
A | G | 1 | a0002c0002t0004g0395 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-976A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604630 | ||||||
| chr1:24604632
|
A | ATGTGTGT others(27): Show |
1 | a0002c0002t0013g0002 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.168-973_168-972ins others(34): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604632 | |||||
| chr1:24604632
|
A | G | 2 | a0002c0002t0004g0395a0002c0002t0013g0146 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168-974A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604632 | ||||||
| chr1:24604633
|
T | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0270 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.168-973T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604633 | ||||||
| chr1:24604634
|
A | G | 3 | a0002c0002t0004g0395a0002c0002t0013g0002a0002c0002t0013g0146 | 4 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-972A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604634 | ||||||
| chr1:24604636
|
A | G | 3 | a0002c0002t0004g0395a0002c0002t0013g0002a0002c0002t0013g0146 | 4 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-970A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604636 | ||||||
| chr1:24604638
|
A | ATGTGTGT others(51): Show |
1 | a0002c0002t0004g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-967_168-966ins others(58): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24604638 | |||||
| chr1:24604638
|
A | G | 3 | a0002c0002t0004g0395a0002c0002t0013g0002a0002c0002t0013g0146 | 4 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-968A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604638 | ||||||
| chr1:24604639
|
T | A | 1 | a0001c0001t0001g0283 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168-967T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604639 | ||||||
| chr1:24604641
|
T | A | 1 | a0001c0001t0001g0283 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168-965T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604641 | ||||||
| chr1:24604644
|
AT | A | 4 | a0002c0002t0004g0004a0002c0002t0004g0395a0002c0002t0013g0002others(1): Show | 5 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-961delT | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604644 | ||||||
| chr1:24604647
|
T | A | 4 | a0002c0002t0004g0004a0002c0002t0004g0395a0002c0002t0013g0002others(1): Show | 5 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-959T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604647 | ||||||
| chr1:24604649
|
T | A | 4 | a0002c0002t0004g0004a0002c0002t0004g0395a0002c0002t0013g0002others(1): Show | 5 | HG01891.hp2 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-957T>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | ||||||
| chr1:24604649
|
T | TGTGTGTG others(32): Show |
3 | a0002c0002t0004g0017a0002c0002t0004g0025a0002c0002t0004g0057 | 3 | HG01243.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.168-957_168-956ins others(39): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | ||||||
| chr1:24604649
|
T | TGTGTGTG others(34): Show |
6 | a0002c0002t0004g0016a0002c0002t0004g0023a0002c0002t0004g0029others(3): Show | 6 | HG01099.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-957_168-956ins others(41): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | ||||||
| chr1:24604649
|
T | TGTGTGTG others(36): Show |
4 | a0002c0002t0004g0030a0002c0002t0004g0031a0002c0002t0004g0033others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-957_168-956ins others(43): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | ||||||
| chr1:24604649
|
T | TGTGTGTG others(38): Show |
2 | a0002c0002t0004g0391a0002c0002t0004g0393 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.168-957_168-956ins others(45): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | ||||||
| chr1:24604649
|
T | TGTGTGTG others(42): Show |
1 | a0002c0002t0004g0390 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.168-957_168-956ins others(49): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | ||||||
| chr1:24604649
|
T | TGTGTGTG others(52): Show |
1 | a0002c0002t0004g0006 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.168-957_168-956ins others(59): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | ||||||
| chr1:24604649
|
T | TGTGTGTG others(60): Show |
1 | a0002c0002t0004g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.168-957_168-956ins others(67): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604649 | ||||||
| chr1:24604671
|
C | T | 227 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0027others(224): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.168-935C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604671 | ||||||
| chr1:24604672
|
C | A | 16 | a0001c0001t0006g0141a0001c0001t0006g0151a0001c0001t0006g0152others(13): Show | 16 | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.168-934C>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604672 | ||||||
| chr1:24604709
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-897T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604709 | ||||||
| chr1:24604779
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.168-827G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604779 | ||||||
| chr1:24604841
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-765A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604841 | ||||||
| chr1:24604872
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168-734T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604872 | ||||||
| chr1:24604873
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168-733G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604873 | ||||||
| chr1:24604913
|
G | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-693G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604913 | ||||||
| chr1:24604953
|
A | T | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-653A>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604953 | ||||||
| chr1:24604988
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-618T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604988 | ||||||
| chr1:24604989
|
G | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-617G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24604989 | ||||||
| chr1:24605010
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.168-596G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605010 | ||||||
| chr1:24605076
|
A | G | 14 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(11): Show | 15 | HG01099.hp2 HG01891.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-530A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605076 | ||||||
| chr1:24605094
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-512T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605094 | ||||||
| chr1:24605106
|
A | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-500A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605106 | ||||||
| chr1:24605123
|
GAA | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-473_168-472del others(2): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 24605123 | |||||
| chr1:24605220
|
T | C | 1 | a0001c0001t0008g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.168-386T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605220 | ||||||
| chr1:24605360
|
C | T | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-246C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605360 | ||||||
| chr1:24605376
|
T | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-230T>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605376 | ||||||
| chr1:24605435
|
G | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-171G>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605435 | ||||||
| chr1:24605448
|
A | C | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-158A>C | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605448 | ||||||
| chr1:24605503
|
A | G | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-103A>G | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605503 | ||||||
| chr1:24605539
|
C | T | 1 | a0002c0002t0004g0395 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168-67C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605539 | ||||||
| chr1:24605555
|
C | T | 1 | a0001c0001t0003g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168-51C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605555 | ||||||
| chr1:24605556
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0257a0001c0001t0001g0262 | 3 | HG00423.hp1 HG02074.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.168-50G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605556 | ||||||
| chr1:24605557
|
C | T | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-49C>T | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605557 | ||||||
| chr1:24605570
|
G | A | 22 | a0002c0002t0004g0004a0002c0002t0004g0006a0002c0002t0004g0016others(19): Show | 23 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.168-36G>A | NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | chr1 | 24605570 |