| geneid | 8439 |
|---|---|
| ensemblid | ENSG00000035681.9 |
| hgncid | 8017 |
| symbol | NSMAF |
| name | neutral sphingomyelinase activation associated factor |
| refseq_nuc | NM_003580.4 |
| refseq_prot | NP_003571.2 |
| ensembl_nuc | ENST00000038176.8 |
| ensembl_prot | ENSP00000038176.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 58583508 |
| end | 58659853 |
| strand | - |
| ver | v1.2 |
| region | chr8:58583508-58659853 |
| region5000 | chr8:58578508-58664853 |
| regionname0 | NSMAF_chr8_58583508_58659853 |
| regionname5000 | NSMAF_chr8_58578508_58664853 |
| 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 | 917 | 290 | 74 | 50 | 121 | 14 | 29 | 98 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0002 | 0/0 | 917 | 64 | 8 | 2 | 52 | 0 | 2 | 43 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0003 | 0/0 | 917 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0004 | 0/0 | 917 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0005 | 0/0 | 917 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0006 | 0/0 | 917 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0007 | 0/0 | 917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0008 | 0/0 | 917 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0009 | 0/0 | 917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2754 | 251 | 53 | 41 | 118 | 12 | 26 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0002 | 0/0 | 2754 | 63 | 7 | 2 | 52 | 0 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0003 | 1/0 | 2754 | 28 | 15 | 6 | 2 | 2 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0004 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0005 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0006 | 0/0 | 2754 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0007 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0008 | 0/0 | 2754 | 2 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0009 | 0/0 | 2754 | 2 | 0 | 2 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0010 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0011 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0012 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0013 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0014 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0015 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0016 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0017 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| c0018 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| 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 | 821 | 240 | 56 | 38 | 117 | 8 | 20 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0002 | 0/1 | 821 | 77 | 8 | 12 | 38 | 6 | 12 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0003 | 0/0 | 821 | 15 | 14 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0004 | 0/0 | 821 | 12 | 0 | 0 | 12 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0005 | 0/0 | 821 | 5 | 0 | 0 | 5 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0006 | 0/0 | 821 | 4 | 3 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0007 | 0/0 | 821 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0008 | 0/0 | 821 | 3 | 3 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0009 | 0/0 | 821 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0010 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0011 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0012 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0013 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0014 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0015 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| t0016 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0289 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2754 | 251 | 53 | 41 | 118 | 12 | 26 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0003 | 1/0 | 2754 | 28 | 15 | 6 | 2 | 2 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0004 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0008 | 0/0 | 2754 | 2 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0009 | 0/0 | 2754 | 2 | 0 | 2 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0010 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0011 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0017 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0002c0002 | 0/0 | 2754 | 63 | 7 | 2 | 52 | 0 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0002c0013 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0003c0005 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0004c0006 | 0/0 | 2754 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0005c0015 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0005c0016 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0006c0007 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0007c0014 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0008c0012 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0009c0018 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3574 | 150 | 29 | 28 | 72 | 6 | 15 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0002 | 0/1 | 3574 | 69 | 6 | 11 | 34 | 6 | 11 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0003 | 0/0 | 3574 | 11 | 10 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0004 | 0/0 | 3574 | 6 | 0 | 0 | 6 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0006 | 0/0 | 3574 | 2 | 1 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0007 | 0/0 | 3574 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0008 | 0/0 | 3574 | 3 | 3 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0010 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0011 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0012 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0013 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0014 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0015 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0001t0016 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0003t0001 | 1/0 | 3574 | 27 | 14 | 6 | 2 | 2 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0003t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0004t0001 | 0/0 | 3574 | 4 | 4 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0008t0002 | 0/0 | 3574 | 2 | 0 | 1 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0009t0001 | 0/0 | 3574 | 2 | 0 | 2 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0010t0006 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0011t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0001c0017t0001 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0002c0002t0001 | 0/0 | 3574 | 50 | 6 | 2 | 40 | 0 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0002c0002t0002 | 0/0 | 3574 | 2 | 1 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0002c0002t0004 | 0/0 | 3574 | 6 | 0 | 0 | 6 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0002c0002t0005 | 0/0 | 3574 | 5 | 0 | 0 | 5 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0002c0013t0001 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0003c0005t0001 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0003c0005t0002 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0003c0005t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0003c0005t0009 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0004c0006t0001 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0004c0006t0002 | 0/0 | 3574 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0005c0015t0009 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0005c0016t0006 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0006c0007t0001 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0006c0007t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0007c0014t0001 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0008c0012t0001 | 0/0 | 3574 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| a0009c0018t0002 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | copy fasta | chr8 | 58578508 | 58664853 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0012g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0014g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0001t0016g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0289 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0008t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0008t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0009t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0009t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0010t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0011t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0001c0017t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0005g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0002t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0002c0013t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0003c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0003c0005t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0003c0005t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0003c0005t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0004c0006t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0004c0006t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0004c0006t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0005c0015t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0005c0016t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0006c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0006c0007t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0007c0014t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0008c0012t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| a0009c0018t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0012 | EUR | GBR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0322 | EUR | GBR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0306 | EUR | GBR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | FIN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00408 | hp1 | a0004 | c0006 | t0002 | g0346 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00597 | hp2 | a0001 | c0017 | t0001 | g0128 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0086 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01070 | hp2 | a0001 | c0009 | t0001 | g0251 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01071 | hp1 | a0001 | c0009 | t0001 | g0252 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0333 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0174 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | IBS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0317 | EUR | IBS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0305 | EUR | IBS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0135 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0258 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0300 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01993 | hp1 | a0001 | c0008 | t0002 | g0316 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02071 | hp2 | a0001 | c0001 | t0013 | g0158 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02074 | hp1 | a0004 | c0006 | t0001 | g0344 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02080 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0341 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02572 | hp1 | a0005 | c0016 | t0006 | g0102 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02622 | hp1 | a0002 | c0013 | t0001 | g0197 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0202 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0193 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0113 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0299 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02738 | hp1 | a0001 | c0008 | t0002 | g0315 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0085 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02818 | hp2 | a0001 | c0011 | t0003 | g0050 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0210 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0039 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02976 | hp2 | a0001 | c0001 | t0014 | g0260 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0339 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0218 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0106 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03130 | hp1 | a0001 | c0010 | t0006 | g0112 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03130 | hp2 | a0003 | c0005 | t0009 | g0035 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0042 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0116 | AFR | ESN | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03540 | hp1 | a0006 | c0007 | t0001 | g0103 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0111 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03579 | hp2 | a0003 | c0005 | t0003 | g0044 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0338 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04204 | hp1 | a0008 | c0012 | t0001 | g0294 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | STU | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18747 | hp1 | a0002 | c0002 | t0004 | g0026 | EAS | CHB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | CHB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18906 | hp2 | a0003 | c0005 | t0001 | g0212 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18945 | hp2 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18952 | hp1 | a0004 | c0006 | t0002 | g0345 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0020 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18961 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18973 | hp1 | a0001 | c0001 | t0015 | g0131 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18985 | hp1 | a0007 | c0014 | t0001 | g0140 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18987 | hp1 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18990 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18992 | hp2 | a0002 | c0002 | t0004 | g0023 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18995 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | LWK | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19055 | hp1 | a0002 | c0002 | t0005 | g0018 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19057 | hp1 | a0009 | c0018 | t0002 | g0120 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19072 | hp1 | a0002 | c0002 | t0005 | g0019 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19083 | hp2 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19086 | hp1 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ASW | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ASW | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0309 | EUR | TSI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | TSI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | TSI | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | GIH | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0298 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0037 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03471 | hp1 | a0005 | c0015 | t0009 | g0034 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20300 | hp1 | a0003 | c0005 | t0002 | g0207 | AFR | USA | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| NA21309 | hp2 | a0006 | c0007 | t0003 | g0038 | AFR | LWK | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0318 | REF | REF | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0289 | REF | REF | NSMAF_chr8_58578508_58664853 | NSMAF | chr8 | 58578508 | 58664853 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58587638
|
C | T | 1 | a0008 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2275G>A | p.Glu759Lys | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/31 | 2497/3574 | 2275/2754 | 759/917 | chr8 | 58587638 | ||
| chr8:58589547
|
G | A | 1 | a0007 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.2116C>T | p.Arg706Cys | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/31 | 2338/3574 | 2116/2754 | 706/917 | chr8 | 58589547 | ||
| chr8:58595575
|
T | C | 2 | a0002a0007 | 65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
missense_variant | MODERATE | c.1877A>G | p.Tyr626Cys | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/31 | 2099/3574 | 1877/2754 | 626/917 | chr8 | 58595575 | ||
| chr8:58599358
|
C | T | 1 | a0006 | 2 | HG03540.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1459G>A | p.Glu487Lys | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/31 | 1681/3574 | 1459/2754 | 487/917 | chr8 | 58599358 | ||
| chr8:58599762
|
G | C | 1 | a0005 | 2 | HG02572.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.1441C>G | p.Pro481Ala | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/31 | 1663/3574 | 1441/2754 | 481/917 | chr8 | 58599762 | ||
| chr8:58603374
|
G | A | 1 | a0003 | 4 | HG03130.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
missense_variant | MODERATE | c.881C>T | p.Ala294Val | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/31 | 1103/3574 | 881/2754 | 294/917 | chr8 | 58603374 | ||
| chr8:58631527
|
T | C | 1 | a0009 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.353A>G | p.His118Arg | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/31 | 575/3574 | 353/2754 | 118/917 | chr8 | 58631527 | ||
| chr8:58659589
|
G | C | 1 | a0004 | 3 | HG00408.hp1 HG02074.hp1 NA18952.hp1 |
missense_variant | MODERATE | c.43C>G | p.Leu15Val | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 265/3574 | 43/2754 | 15/917 | chr8 | 58659589 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58589470
|
C | T | 2 | a0001c0004a0005c0015 | 5 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.2193G>A | p.Ser731Ser | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/31 | 2415/3574 | 2193/2754 | 731/917 | chr8 | 58589470 | ||
| chr8:58589518
|
A | G | 1 | a0002c0013 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.2145T>C | p.Asp715Asp | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/31 | 2367/3574 | 2145/2754 | 715/917 | chr8 | 58589518 | ||
| chr8:58595607
|
A | G | 1 | a0001c0008 | 2 | HG01993.hp1 HG02738.hp1 |
synonymous_variant | LOW | c.1845T>C | p.Asn615Asn | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/31 | 2067/3574 | 1845/2754 | 615/917 | chr8 | 58595607 | ||
| chr8:58597505
|
C | T | 2 | a0001c0010a0001c0011 | 2 | HG02818.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1674G>A | p.Leu558Leu | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/31 | 1896/3574 | 1674/2754 | 558/917 | chr8 | 58597505 | ||
| chr8:58599775
|
G | A | 16 | a0001c0001a0001c0004a0001c0008others(13): Show | 339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
synonymous_variant | LOW | c.1428C>T | p.Asp476Asp | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/31 | 1650/3574 | 1428/2754 | 476/917 | chr8 | 58599775 | ||
| chr8:58606005
|
G | A | 1 | a0001c0017 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.790C>T | p.Leu264Leu | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/31 | 1012/3574 | 790/2754 | 264/917 | chr8 | 58606005 | ||
| chr8:58609655
|
G | A | 1 | a0001c0009 | 2 | HG01070.hp2 HG01071.hp1 |
synonymous_variant | LOW | c.636C>T | p.His212His | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/31 | 858/3574 | 636/2754 | 212/917 | chr8 | 58609655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58583565
|
C | G | 1 | a0001c0001t0014 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 541 | chr8 | 58583565 | |||||
| chr8:58583817
|
A | C | 3 | a0001c0001t0008a0001c0001t0012a0001c0001t0016 | 5 | HG02615.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*289T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 289 | chr8 | 58583817 | |||||
| chr8:58583857
|
C | T | 11 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(8): Show | 84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*249G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 249 | chr8 | 58583857 | |||||
| chr8:58583927
|
G | A | 1 | a0001c0001t0015 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*179C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 179 | chr8 | 58583927 | |||||
| chr8:58583931
|
A | G | 14 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(11): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*175T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 175 | chr8 | 58583931 | |||||
| chr8:58584004
|
C | T | 1 | a0001c0001t0013 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 31/31 | 102 | chr8 | 58584004 | |||||
| chr8:58659752
|
G | T | 2 | a0003c0005t0009a0005c0015t0009 | 2 | HG03130.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-121C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 121 | chr8 | 58659752 | |||||
| chr8:58659781
|
G | T | 10 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(7): Show | 22 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-150C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 150 | chr8 | 58659781 | |||||
| chr8:58659797
|
C | T | 3 | a0001c0001t0004a0001c0001t0007a0002c0002t0004 | 15 | HG02080.hp1 NA18747.hp1 NA18747.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-166G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 166 | chr8 | 58659797 | |||||
| chr8:58659821
|
A | G | 2 | a0001c0001t0010a0002c0002t0005 | 6 | NA18960.hp1 NA18961.hp1 NA18990.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-190T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/31 | 190 | chr8 | 58659821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:58584375
|
C | T | 78 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0104others(75): Show | 85 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.2660-175G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584375 | ||||||
| chr8:58584510
|
C | CAAAAGTT others(346): Show |
1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2660-311_2660-310i others(355): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584510 | ||||||
| chr8:58584782
|
G | A | 1 | a0002c0002t0001g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2660-582C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584782 | ||||||
| chr8:58584812
|
G | A | 89 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(86): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2660-612C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584812 | ||||||
| chr8:58584836
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2660-636C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584836 | ||||||
| chr8:58584838
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2660-638A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584838 | ||||||
| chr8:58584940
|
G | T | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2659+712C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58584940 | ||||||
| chr8:58585185
|
T | G | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2659+467A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585185 | ||||||
| chr8:58585266
|
G | A | 3 | a0001c0001t0001g0136a0003c0005t0001g0212a0003c0005t0009g0035 | 3 | HG02451.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2659+386C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585266 | ||||||
| chr8:58585302
|
T | C | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2659+350A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585302 | ||||||
| chr8:58585317
|
G | GT | 31 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0121others(28): Show | 32 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.2659+334dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | ||||||
| chr8:58585317
|
G | GTTATTTT others(7): Show |
1 | a0001c0003t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2659+334_2659+335i others(16): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | ||||||
| chr8:58585317
|
G | GTTATTTT others(8): Show |
9 | a0001c0001t0001g0138a0001c0003t0001g0010a0001c0003t0001g0105others(6): Show | 10 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2659+334_2659+335i others(17): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | ||||||
| chr8:58585317
|
G | GTTATTTT others(9): Show |
1 | a0001c0003t0001g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2659+334_2659+335i others(18): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | ||||||
| chr8:58585317
|
G | GTTTTTTT others(3): Show |
3 | a0001c0004t0001g0135a0001c0004t0001g0202a0001c0004t0001g0210 | 3 | HG01884.hp2 HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2659+325_2659+334d others(12): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | ||||||
| chr8:58585317
|
G | GTTTTTTT others(5): Show |
1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2659+323_2659+334d others(14): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | ||||||
| chr8:58585317
|
G | GTTTTTTT others(6): Show |
1 | a0005c0015t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2659+334_2659+335i others(15): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585317 | ||||||
| chr8:58585347
|
T | C | 1 | a0001c0008t0002g0316 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2659+305A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585347 | ||||||
| chr8:58585564
|
CAA | C | 11 | a0001c0001t0001g0138a0001c0003t0001g0010a0001c0003t0001g0105others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2659+86_2659+87del others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585564 | ||||||
| chr8:58585631
|
G | A | 194 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0093others(191): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.2659+21C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 30/30 | chr8 | 58585631 | ||||||
| chr8:58585855
|
A | T | 78 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0104others(75): Show | 85 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.2549+43T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 29/30 | chr8 | 58585855 | ||||||
| chr8:58585861
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2549+37C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 29/30 | chr8 | 58585861 | ||||||
| chr8:58585874
|
C | T | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2549+24G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 29/30 | chr8 | 58585874 | ||||||
| chr8:58586035
|
A | G | 11 | a0001c0001t0001g0138a0001c0003t0001g0010a0001c0003t0001g0105others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2447-35T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586035 | ||||||
| chr8:58586049
|
G | T | 5 | a0001c0001t0008g0036a0001c0001t0008g0041a0001c0001t0008g0051others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2447-49C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586049 | ||||||
| chr8:58586055
|
A | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0093others(188): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2447-55T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586055 | ||||||
| chr8:58586115
|
A | T | 1 | a0001c0003t0001g0258 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2447-115T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586115 | ||||||
| chr8:58586126
|
T | G | 69 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.2447-126A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586126 | ||||||
| chr8:58586156
|
T | A | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2447-156A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586156 | ||||||
| chr8:58586181
|
A | C | 5 | a0001c0004t0001g0116a0001c0004t0001g0135a0001c0004t0001g0202others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2447-181T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586181 | ||||||
| chr8:58586209
|
T | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115 | 3 | HG01109.hp1 HG02886.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2447-209A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586209 | ||||||
| chr8:58586215
|
T | C | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2447-215A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586215 | ||||||
| chr8:58586439
|
T | TAAAAAGG others(311): Show |
5 | a0001c0004t0001g0116a0001c0004t0001g0135a0001c0004t0001g0202others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2446+18_2446+19ins others(318): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586439 | ||||||
| chr8:58586439
|
T | TAAAAAGG others(314): Show |
10 | a0001c0001t0001g0138a0001c0003t0001g0010a0001c0003t0001g0106others(7): Show | 11 | HG01884.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2446+18_2446+19ins others(321): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586439 | ||||||
| chr8:58586439
|
T | TAAAAAGG others(315): Show |
1 | a0001c0003t0001g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2446+18_2446+19ins others(322): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 28/30 | chr8 | 58586439 | ||||||
| chr8:58586678
|
G | A | 86 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(83): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.2296-70C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58586678 | ||||||
| chr8:58586731
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2296-123C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58586731 | ||||||
| chr8:58586830
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 127 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2296-222A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58586830 | ||||||
| chr8:58587204
|
C | G | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2295+414G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58587204 | ||||||
| chr8:58587558
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2295+60G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58587558 | ||||||
| chr8:58587564
|
G | A | 1 | a0002c0002t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2295+54C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58587564 | ||||||
| chr8:58587574
|
A | T | 1 | a0002c0002t0004g0024 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2295+44T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 27/30 | chr8 | 58587574 | ||||||
| chr8:58588160
|
C | T | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2212-459G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588160 | ||||||
| chr8:58588228
|
G | A | 1 | a0001c0001t0002g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2212-527C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588228 | ||||||
| chr8:58588334
|
CT | C | 83 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0104others(80): Show | 90 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.2212-634delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588334 | ||||||
| chr8:58588367
|
A | T | 85 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2212-666T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588367 | ||||||
| chr8:58588466
|
T | C | 85 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2212-765A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588466 | ||||||
| chr8:58588578
|
A | C | 85 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2211+874T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588578 | ||||||
| chr8:58588588
|
A | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0093others(188): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2211+864T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588588 | ||||||
| chr8:58588634
|
A | G | 2 | a0006c0007t0001g0103a0006c0007t0003g0038 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2211+818T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588634 | ||||||
| chr8:58588677
|
T | G | 1 | a0001c0003t0001g0341 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2211+775A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588677 | ||||||
| chr8:58588700
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2211+752G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588700 | ||||||
| chr8:58588713
|
C | A | 1 | a0009c0018t0002g0120 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2211+739G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588713 | ||||||
| chr8:58588714
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01167.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2211+738C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588714 | ||||||
| chr8:58588724
|
C | A | 84 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(81): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2211+728G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588724 | ||||||
| chr8:58588725
|
C | A | 1 | a0001c0001t0002g0337 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2211+727G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588725 | ||||||
| chr8:58588755
|
T | C | 11 | a0001c0001t0001g0138a0001c0003t0001g0010a0001c0003t0001g0105others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2211+697A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588755 | ||||||
| chr8:58588824
|
A | G | 6 | a0001c0001t0001g0069a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02074.hp2 NA18963.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2211+628T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588824 | ||||||
| chr8:58588903
|
C | T | 1 | a0001c0003t0001g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2211+549G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58588903 | ||||||
| chr8:58589028
|
A | T | 4 | a0002c0002t0001g0011a0002c0002t0001g0221a0002c0002t0004g0006others(1): Show | 6 | NA18943.hp1 NA18945.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211+424T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589028 | ||||||
| chr8:58589208
|
T | A | 85 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2211+244A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589208 | ||||||
| chr8:58589256
|
G | A | 191 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0093others(188): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2211+196C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589256 | ||||||
| chr8:58589304
|
G | A | 85 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2211+148C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589304 | ||||||
| chr8:58589403
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0273 | 2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2211+49A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589403 | ||||||
| chr8:58589414
|
A | G | 1 | a0005c0015t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2211+38T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 26/30 | chr8 | 58589414 | ||||||
| chr8:58589722
|
C | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115 | 3 | HG01109.hp1 HG02886.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2088-147G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589722 | ||||||
| chr8:58589745
|
A | T | 1 | a0001c0001t0002g0275 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2088-170T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589745 | ||||||
| chr8:58589808
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2087+199G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589808 | ||||||
| chr8:58589908
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2087+99C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589908 | ||||||
| chr8:58589976
|
G | A | 12 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0100others(9): Show | 12 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2087+31C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 25/30 | chr8 | 58589976 | ||||||
| chr8:58590107
|
A | C | 1 | a0001c0001t0002g0275 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2020-33T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590107 | ||||||
| chr8:58590202
|
A | G | 3 | a0001c0001t0001g0136a0003c0005t0001g0212a0003c0005t0009g0035 | 3 | HG02451.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2020-128T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590202 | ||||||
| chr8:58590366
|
T | C | 85 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0015others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2020-292A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590366 | ||||||
| chr8:58590657
|
C | A | 3 | a0001c0001t0006g0053a0001c0001t0006g0086a0001c0010t0006g0112 | 3 | HG00741.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2019+210G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590657 | ||||||
| chr8:58590766
|
A | G | 1 | a0002c0002t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2019+101T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590766 | ||||||
| chr8:58590783
|
G | A | 5 | a0001c0004t0001g0116a0001c0004t0001g0135a0001c0004t0001g0202others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019+84C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 24/30 | chr8 | 58590783 | ||||||
| chr8:58591082
|
G | T | 1 | a0001c0001t0001g0267 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1952-148C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591082 | ||||||
| chr8:58591150
|
A | G | 1 | a0002c0002t0001g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1952-216T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591150 | ||||||
| chr8:58591210
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1952-276G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591210 | ||||||
| chr8:58591248
|
G | A | 3 | a0001c0001t0006g0053a0001c0001t0006g0086a0001c0010t0006g0112 | 3 | HG00741.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1952-314C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591248 | ||||||
| chr8:58591268
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1952-334A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591268 | ||||||
| chr8:58591279
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1952-345T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591279 | ||||||
| chr8:58591430
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1952-496C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591430 | ||||||
| chr8:58591471
|
A | T | 4 | a0001c0004t0001g0116a0001c0004t0001g0135a0001c0004t0001g0202others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1952-537T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591471 | ||||||
| chr8:58591481
|
C | CT | 103 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0081others(100): Show | 114 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.1952-548dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591481 | ||||||
| chr8:58591481
|
C | CTT | 19 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0101others(16): Show | 20 | HG00423.hp1 HG00558.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1952-549_1952-548d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591481 | ||||||
| chr8:58591481
|
CT | C | 21 | a0001c0001t0001g0171a0001c0001t0001g0208a0001c0001t0001g0233others(18): Show | 21 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1952-548delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591481 | ||||||
| chr8:58591788
|
C | T | 1 | a0001c0001t0003g0049 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1952-854G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591788 | ||||||
| chr8:58591893
|
C | T | 59 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(56): Show | 65 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1952-959G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58591893 | ||||||
| chr8:58592350
|
G | A | 1 | a0002c0002t0004g0024 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1952-1416C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592350 | ||||||
| chr8:58592352
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0273 | 2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1952-1418G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592352 | ||||||
| chr8:58592466
|
T | C | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1952-1532A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592466 | ||||||
| chr8:58592565
|
GA | G | 331 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(328): Show | 352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.1952-1632delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592565 | ||||||
| chr8:58592707
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1951+1525C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592707 | ||||||
| chr8:58592746
|
G | C | 1 | a0001c0001t0011g0039 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1951+1486C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592746 | ||||||
| chr8:58592763
|
T | C | 2 | a0001c0001t0002g0181a0001c0001t0002g0306 | 2 | HG00140.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1951+1469A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592763 | ||||||
| chr8:58592805
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1951+1427A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592805 | ||||||
| chr8:58592819
|
G | A | 189 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(186): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1951+1413C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592819 | ||||||
| chr8:58592902
|
C | CA | 9 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0199others(6): Show | 9 | HG00408.hp1 HG01891.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1951+1329dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592902 | ||||||
| chr8:58592906
|
AAC | A | 3 | a0003c0005t0001g0212a0003c0005t0002g0207a0003c0005t0009g0035 | 3 | HG03130.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1951+1324_1951+132 others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592906 | ||||||
| chr8:58592908
|
C | A | 16 | a0001c0001t0001g0138a0001c0001t0002g0052a0001c0001t0002g0099others(13): Show | 16 | HG00408.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1951+1324G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592908 | ||||||
| chr8:58592909
|
AAC | A | 140 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(137): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1951+1321_1951+132 others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592909 | ||||||
| chr8:58592910
|
AC | A | 42 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0104others(39): Show | 44 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1951+1321delG | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592910 | ||||||
| chr8:58592911
|
C | A | 25 | a0001c0001t0001g0138a0001c0001t0002g0052a0001c0001t0002g0099others(22): Show | 25 | HG00408.hp1 HG00735.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1951+1321G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592911 | ||||||
| chr8:58592913
|
A | C | 2 | a0006c0007t0001g0103a0006c0007t0003g0038 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1951+1319T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592913 | ||||||
| chr8:58592914
|
C | A | 75 | a0001c0001t0001g0138a0001c0001t0002g0052a0001c0001t0002g0099others(72): Show | 81 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1951+1318G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592914 | ||||||
| chr8:58592915
|
AAC | A | 38 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0104others(35): Show | 40 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1951+1315_1951+131 others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592915 | ||||||
| chr8:58592916
|
AC | A | 89 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(86): Show | 91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1951+1315delG | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592916 | ||||||
| chr8:58592917
|
C | A | 80 | a0001c0001t0001g0138a0001c0001t0002g0052a0001c0001t0002g0099others(77): Show | 86 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1951+1315G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592917 | ||||||
| chr8:58592919
|
A | C | 86 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(83): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1951+1313T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592919 | ||||||
| chr8:58592923
|
A | C | 1 | a0002c0002t0001g0221 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1951+1309T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592923 | ||||||
| chr8:58592940
|
T | G | 3 | a0001c0001t0001g0104a0001c0001t0003g0007a0001c0001t0003g0043 | 4 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1951+1292A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58592940 | ||||||
| chr8:58593092
|
A | T | 1 | a0001c0001t0001g0183 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1951+1140T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593092 | ||||||
| chr8:58593123
|
T | C | 11 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0100others(8): Show | 11 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1951+1109A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593123 | ||||||
| chr8:58593453
|
C | A | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1951+779G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593453 | ||||||
| chr8:58593473
|
T | G | 207 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(204): Show | 217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1951+759A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593473 | ||||||
| chr8:58593544
|
C | T | 5 | a0001c0001t0001g0138a0001c0004t0001g0116a0001c0004t0001g0135others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1951+688G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593544 | ||||||
| chr8:58593570
|
A | G | 207 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(204): Show | 217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1951+662T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593570 | ||||||
| chr8:58593592
|
T | C | 5 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0256others(2): Show | 5 | NA18747.hp2 NA18954.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951+640A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593592 | ||||||
| chr8:58593624
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1951+608A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593624 | ||||||
| chr8:58593628
|
G | A | 207 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(204): Show | 217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1951+604C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593628 | ||||||
| chr8:58593675
|
A | G | 17 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0100others(14): Show | 17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1951+557T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593675 | ||||||
| chr8:58593936
|
C | G | 17 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0100others(14): Show | 17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1951+296G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58593936 | ||||||
| chr8:58594114
|
A | G | 2 | a0006c0007t0001g0103a0006c0007t0003g0038 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1951+118T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58594114 | ||||||
| chr8:58594142
|
C | A | 1 | a0001c0001t0002g0250 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1951+90G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58594142 | ||||||
| chr8:58594209
|
G | A | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1951+23C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58594209 | ||||||
| chr8:58594215
|
C | T | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1951+17G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 23/30 | chr8 | 58594215 | ||||||
| chr8:58594355
|
T | C | 1 | a0001c0001t0002g0201 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1893-65A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594355 | ||||||
| chr8:58594412
|
C | T | 5 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0001t0003g0007others(2): Show | 6 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1893-122G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594412 | ||||||
| chr8:58594566
|
G | A | 17 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0100others(14): Show | 17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1893-276C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594566 | ||||||
| chr8:58594595
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0003g0007a0001c0001t0003g0043 | 4 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-305C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594595 | ||||||
| chr8:58594636
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1893-346G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594636 | ||||||
| chr8:58594680
|
AATG | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0126a0001c0001t0001g0302 | 3 | NA19060.hp1 NA19080.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1893-393_1893-391d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594680 | ||||||
| chr8:58594796
|
T | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0173others(26): Show | 34 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.1893-506A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594796 | ||||||
| chr8:58594912
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(54): Show | 63 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1893-622C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58594912 | ||||||
| chr8:58595114
|
A | ATTG | 17 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0100others(14): Show | 17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1892+445_1892+446i others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595114 | ||||||
| chr8:58595226
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1892+334G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595226 | ||||||
| chr8:58595313
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1892+247A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595313 | ||||||
| chr8:58595391
|
A | C | 187 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(184): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1892+169T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595391 | ||||||
| chr8:58595517
|
A | G | 202 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(199): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1892+43T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 22/30 | chr8 | 58595517 | ||||||
| chr8:58595685
|
CT | C | 86 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(83): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1793-27delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58595685 | ||||||
| chr8:58595781
|
T | C | 2 | a0001c0001t0002g0256a0001c0001t0007g0030 | 2 | NA18747.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1793-122A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58595781 | ||||||
| chr8:58595816
|
C | T | 187 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(184): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1793-157G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58595816 | ||||||
| chr8:58595874
|
G | C | 59 | a0002c0002t0001g0001a0002c0002t0001g0011a0002c0002t0001g0055others(56): Show | 65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1793-215C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58595874 | ||||||
| chr8:58596021
|
C | T | 17 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0100others(14): Show | 17 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1793-362G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596021 | ||||||
| chr8:58596185
|
A | T | 1 | a0001c0001t0007g0029 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1793-526T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596185 | ||||||
| chr8:58596288
|
T | C | 59 | a0002c0002t0001g0001a0002c0002t0001g0011a0002c0002t0001g0055others(56): Show | 65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1793-629A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596288 | ||||||
| chr8:58596404
|
A | G | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1793-745T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596404 | ||||||
| chr8:58596428
|
T | C | 13 | a0001c0001t0002g0052a0001c0001t0002g0099a0001c0001t0002g0100others(10): Show | 13 | HG00408.hp1 HG00735.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1793-769A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596428 | ||||||
| chr8:58596430
|
G | C | 6 | a0001c0001t0001g0253a0001c0001t0008g0036a0001c0001t0008g0041others(3): Show | 6 | HG02615.hp2 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1793-771C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596430 | ||||||
| chr8:58596564
|
G | C | 2 | a0006c0007t0001g0103a0006c0007t0003g0038 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1792+823C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596564 | ||||||
| chr8:58596796
|
C | T | 55 | a0001c0001t0001g0240a0002c0002t0001g0001a0002c0002t0001g0011others(52): Show | 61 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1792+591G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596796 | ||||||
| chr8:58596844
|
C | T | 1 | a0001c0001t0006g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1792+543G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596844 | ||||||
| chr8:58596868
|
T | C | 1 | a0001c0001t0002g0336 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1792+519A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596868 | ||||||
| chr8:58596925
|
C | A | 1 | a0005c0015t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1792+462G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596925 | ||||||
| chr8:58596930
|
C | CA | 6 | a0001c0001t0002g0181a0001c0001t0002g0255a0001c0001t0002g0306others(3): Show | 6 | HG00140.hp2 HG00642.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+456dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596930 | ||||||
| chr8:58596930
|
CA | C | 19 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(16): Show | 19 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1792+456delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58596930 | ||||||
| chr8:58597034
|
G | T | 6 | a0001c0001t0001g0253a0001c0001t0008g0036a0001c0001t0008g0041others(3): Show | 6 | HG02615.hp2 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792+353C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597034 | ||||||
| chr8:58597128
|
C | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0278a0001c0001t0013g0158 | 3 | HG00673.hp2 HG02071.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1792+259G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597128 | ||||||
| chr8:58597141
|
G | T | 1 | a0001c0001t0007g0029 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1792+246C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597141 | ||||||
| chr8:58597156
|
T | C | 15 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(12): Show | 15 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1792+231A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597156 | ||||||
| chr8:58597261
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1792+126A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597261 | ||||||
| chr8:58597305
|
C | T | 2 | a0001c0003t0001g0299a0001c0003t0001g0339 | 2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1792+82G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597305 | ||||||
| chr8:58597326
|
A | T | 3 | a0001c0001t0002g0088a0001c0001t0002g0090a0001c0001t0002g0092 | 3 | NA18969.hp2 NA18970.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1792+61T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 21/30 | chr8 | 58597326 | ||||||
| chr8:58597553
|
T | A | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.1629-3A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597553 | ||||||
| chr8:58597575
|
C | T | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1629-25G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597575 | ||||||
| chr8:58597646
|
C | T | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1629-96G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597646 | ||||||
| chr8:58597701
|
C | A | 2 | a0006c0007t0001g0103a0006c0007t0003g0038 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1629-151G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597701 | ||||||
| chr8:58597785
|
A | G | 1 | a0002c0002t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1628+75T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 20/30 | chr8 | 58597785 | ||||||
| chr8:58597917
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1586-15G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58597917 | ||||||
| chr8:58598102
|
T | G | 2 | a0002c0002t0001g0065a0002c0002t0005g0018 | 2 | NA18955.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1586-200A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598102 | ||||||
| chr8:58598309
|
T | C | 147 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(144): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1586-407A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598309 | ||||||
| chr8:58598353
|
T | A | 2 | a0006c0007t0001g0103a0006c0007t0003g0038 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1586-451A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598353 | ||||||
| chr8:58598490
|
CA | C | 63 | a0001c0001t0001g0089a0001c0001t0001g0129a0001c0001t0001g0130others(60): Show | 64 | HG00408.hp2 HG00673.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1586-589delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | ||||||
| chr8:58598490
|
CAAA | C | 13 | a0001c0001t0001g0138a0001c0001t0001g0253a0001c0001t0006g0053others(10): Show | 13 | HG00741.hp2 HG01884.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1586-591_1586-589d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | ||||||
| chr8:58598490
|
CAAAA | C | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(5): Show | 8 | HG01069.hp1 HG01192.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1586-592_1586-589d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | ||||||
| chr8:58598490
|
CAAAAAAA others(1): Show |
C | 59 | a0002c0002t0001g0001a0002c0002t0001g0011a0002c0002t0001g0055others(56): Show | 65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1586-596_1586-589d others(10): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | ||||||
| chr8:58598490
|
CAAAAAAA others(7): Show |
C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1586-602_1586-589d others(16): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598490 | ||||||
| chr8:58598506
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1586-604T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598506 | ||||||
| chr8:58598567
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0142others(12): Show | 17 | HG00438.hp2 HG00609.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.1585+665C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598567 | ||||||
| chr8:58598570
|
C | T | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1585+662G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598570 | ||||||
| chr8:58598591
|
T | C | 1 | a0001c0001t0006g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1585+641A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598591 | ||||||
| chr8:58598687
|
A | G | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(312): Show | 334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1585+545T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598687 | ||||||
| chr8:58598751
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1585+481T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598751 | ||||||
| chr8:58598824
|
A | G | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1585+408T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598824 | ||||||
| chr8:58598849
|
C | CCT | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(312): Show | 334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1585+382_1585+383i others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598849 | ||||||
| chr8:58598854
|
C | T | 15 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(12): Show | 15 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1585+378G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598854 | ||||||
| chr8:58598861
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1585+371T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598861 | ||||||
| chr8:58598987
|
C | T | 15 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(12): Show | 15 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1585+245G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58598987 | ||||||
| chr8:58599075
|
G | A | 1 | a0001c0003t0001g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1585+157C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58599075 | ||||||
| chr8:58599178
|
A | G | 1 | a0002c0002t0001g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1585+54T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58599178 | ||||||
| chr8:58599197
|
C | T | 147 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(144): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1585+35G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 19/30 | chr8 | 58599197 | ||||||
| chr8:58599535
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1454-172C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/30 | chr8 | 58599535 | ||||||
| chr8:58599684
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1453+66T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/30 | chr8 | 58599684 | ||||||
| chr8:58599685
|
A | T | 11 | a0001c0001t0001g0138a0001c0001t0001g0253a0001c0001t0008g0036others(8): Show | 11 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1453+65T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 18/30 | chr8 | 58599685 | ||||||
| chr8:58599881
|
C | T | 13 | a0001c0003t0001g0010a0001c0003t0001g0105a0001c0003t0001g0106others(10): Show | 14 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1333-11G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 17/30 | chr8 | 58599881 | ||||||
| chr8:58600085
|
T | A | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1281-64A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600085 | ||||||
| chr8:58600241
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1281-220C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600241 | ||||||
| chr8:58600253
|
G | A | 2 | a0006c0007t0001g0103a0006c0007t0003g0038 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1281-232C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600253 | ||||||
| chr8:58600396
|
G | A | 160 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(157): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1281-375C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600396 | ||||||
| chr8:58600442
|
G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1281-421C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600442 | ||||||
| chr8:58600452
|
A | G | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1281-431T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600452 | ||||||
| chr8:58600484
|
G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1281-463C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600484 | ||||||
| chr8:58600585
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0001t0003g0007others(2): Show | 6 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281-564C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600585 | ||||||
| chr8:58600621
|
C | CA | 23 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0134others(20): Show | 24 | HG00323.hp1 HG00609.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1281-601dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | ||||||
| chr8:58600621
|
C | CAA | 93 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(90): Show | 95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1281-602_1281-601d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | ||||||
| chr8:58600621
|
C | CAAA | 23 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(20): Show | 23 | HG00423.hp2 HG01069.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1281-603_1281-601d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | ||||||
| chr8:58600621
|
C | CAAAA | 36 | a0001c0001t0001g0176a0001c0001t0001g0226a0001c0001t0002g0337others(33): Show | 42 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1281-604_1281-601d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | ||||||
| chr8:58600621
|
C | CAAAAA | 16 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(13): Show | 16 | HG00558.hp2 HG00741.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1281-605_1281-601d others(7): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | ||||||
| chr8:58600621
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1281-611_1281-601d others(13): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600621 | ||||||
| chr8:58600633
|
A | T | 4 | a0003c0005t0001g0212a0003c0005t0002g0207a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281-612T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600633 | ||||||
| chr8:58600639
|
A | AAAAAAAA others(6): Show |
4 | a0003c0005t0001g0212a0003c0005t0002g0207a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281-619_1281-618i others(15): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600639 | ||||||
| chr8:58600768
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1280+517C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600768 | ||||||
| chr8:58600770
|
G | GTAA | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1280+514_1280+515i others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58600770 | ||||||
| chr8:58601154
|
A | T | 1 | a0004c0006t0001g0344 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1280+131T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58601154 | ||||||
| chr8:58601234
|
A | C | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1280+51T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 16/30 | chr8 | 58601234 | ||||||
| chr8:58601546
|
G | GA | 17 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0182others(14): Show | 17 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1126-12dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601546 | ||||||
| chr8:58601546
|
G | GAA | 30 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0104others(27): Show | 32 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1126-13_1126-12dup others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601546 | ||||||
| chr8:58601546
|
G | GAAA | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1126-14_1126-12dup others(3): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601546 | ||||||
| chr8:58601546
|
G | GAAAA | 7 | a0001c0001t0001g0139a0001c0001t0001g0185a0001c0001t0001g0230others(4): Show | 7 | HG00735.hp1 HG03688.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126-15_1126-12dup others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601546 | ||||||
| chr8:58601626
|
A | C | 2 | a0002c0002t0001g0196a0002c0002t0002g0264 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1126-91T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601626 | ||||||
| chr8:58601799
|
T | C | 2 | a0006c0007t0001g0103a0006c0007t0003g0038 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1125+259A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601799 | ||||||
| chr8:58601961
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1125+97A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601961 | ||||||
| chr8:58601976
|
G | A | 58 | a0002c0002t0001g0001a0002c0002t0001g0011a0002c0002t0001g0055others(55): Show | 64 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1125+82C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 14/30 | chr8 | 58601976 | ||||||
| chr8:58602214
|
A | G | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1046-77T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602214 | ||||||
| chr8:58602410
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0278a0001c0001t0013g0158 | 3 | HG00673.hp2 HG02071.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1046-273A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602410 | ||||||
| chr8:58602433
|
C | G | 7 | a0001c0001t0002g0076a0001c0001t0002g0156a0001c0001t0002g0215others(4): Show | 7 | NA18951.hp2 NA18952.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1046-296G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602433 | ||||||
| chr8:58602515
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 142 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1046-378G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602515 | ||||||
| chr8:58602520
|
A | G | 22 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0104others(19): Show | 23 | HG00741.hp2 HG01069.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1046-383T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602520 | ||||||
| chr8:58602569
|
T | A | 316 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.1046-432A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602569 | ||||||
| chr8:58602804
|
G | C | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1045+406C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602804 | ||||||
| chr8:58602843
|
T | A | 1 | a0002c0002t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1045+367A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602843 | ||||||
| chr8:58602855
|
A | G | 1 | a0001c0010t0006g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1045+355T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602855 | ||||||
| chr8:58602953
|
G | A | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1045+257C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58602953 | ||||||
| chr8:58603110
|
C | A | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1045+100G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58603110 | ||||||
| chr8:58603197
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 148 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1045+13C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 13/30 | chr8 | 58603197 | ||||||
| chr8:58603470
|
C | T | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.869-84G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603470 | ||||||
| chr8:58603551
|
A | G | 67 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0253others(64): Show | 73 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.869-165T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603551 | ||||||
| chr8:58603551
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.869-165T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603551 | ||||||
| chr8:58603597
|
C | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 148 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.869-211G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603597 | ||||||
| chr8:58603650
|
G | A | 1 | a0002c0002t0001g0221 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.869-264C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603650 | ||||||
| chr8:58603657
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.869-271C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603657 | ||||||
| chr8:58603725
|
C | CTG | 24 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0104others(21): Show | 25 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.869-341_869-340dup others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603725 | ||||||
| chr8:58603816
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.869-430A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603816 | ||||||
| chr8:58603831
|
T | G | 6 | a0002c0002t0001g0066a0002c0002t0001g0068a0002c0002t0001g0077others(3): Show | 6 | HG01168.hp1 HG02300.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-445A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603831 | ||||||
| chr8:58603849
|
T | G | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.869-463A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603849 | ||||||
| chr8:58603922
|
G | A | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(312): Show | 335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.869-536C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58603922 | ||||||
| chr8:58604379
|
C | A | 66 | a0001c0001t0001g0138a0001c0001t0001g0253a0001c0001t0008g0036others(63): Show | 72 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.869-993G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604379 | ||||||
| chr8:58604499
|
T | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 170 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.869-1113A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604499 | ||||||
| chr8:58604557
|
A | AAT | 22 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(19): Show | 23 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.869-1173_869-1172d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604557 | ||||||
| chr8:58604557
|
A | AATAT | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.869-1175_869-1172d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604557 | ||||||
| chr8:58604758
|
T | G | 2 | a0001c0001t0002g0133a0001c0001t0002g0214 | 2 | HG03098.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.868+1169A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604758 | ||||||
| chr8:58604952
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.868+975G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58604952 | ||||||
| chr8:58605003
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.868+924G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605003 | ||||||
| chr8:58605139
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.868+788G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605139 | ||||||
| chr8:58605161
|
A | G | 9 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(6): Show | 9 | HG01069.hp1 HG01192.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.868+766T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605161 | ||||||
| chr8:58605399
|
A | G | 69 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0253others(66): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.868+528T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605399 | ||||||
| chr8:58605621
|
C | T | 1 | a0002c0002t0001g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.868+306G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605621 | ||||||
| chr8:58605629
|
C | G | 89 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(86): Show | 96 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.868+298G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605629 | ||||||
| chr8:58605784
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+143C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605784 | ||||||
| chr8:58605847
|
T | C | 1 | a0001c0001t0011g0039 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.868+80A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605847 | ||||||
| chr8:58605857
|
G | T | 5 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.868+70C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605857 | ||||||
| chr8:58605880
|
C | CA | 25 | a0001c0001t0001g0081a0001c0001t0001g0132a0001c0001t0001g0139others(22): Show | 26 | HG00621.hp1 HG01167.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.868+46dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605880 | ||||||
| chr8:58605893
|
A | AG | 4 | a0002c0002t0001g0011a0002c0002t0001g0221a0002c0002t0004g0006others(1): Show | 6 | NA18943.hp1 NA18945.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.868+33_868+34insC | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605893 | ||||||
| chr8:58605893
|
A | G | 85 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(82): Show | 90 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.868+34T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 12/30 | chr8 | 58605893 | ||||||
| chr8:58606052
|
A | AAAATAAT others(5): Show |
87 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(84): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.760-29_760-18dupAT others(10): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606052 | ||||||
| chr8:58606205
|
T | G | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.760-170A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606205 | ||||||
| chr8:58606214
|
G | GTA | 3 | a0001c0001t0001g0291a0001c0001t0002g0015a0001c0001t0002g0215 | 4 | HG00738.hp2 HG03704.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-181_760-180dup others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606214 | ||||||
| chr8:58606250
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.760-215C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606250 | ||||||
| chr8:58606398
|
C | G | 3 | a0001c0001t0002g0214a0006c0007t0001g0103a0006c0007t0003g0038 | 3 | HG03098.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.760-363G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606398 | ||||||
| chr8:58606769
|
T | A | 89 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(86): Show | 96 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.760-734A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606769 | ||||||
| chr8:58606842
|
T | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0287a0008c0012t0001g0294 | 3 | HG02735.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.760-807A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606842 | ||||||
| chr8:58606862
|
G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.760-827C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606862 | ||||||
| chr8:58606899
|
T | C | 1 | a0001c0003t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.760-864A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606899 | ||||||
| chr8:58606917
|
T | C | 93 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(90): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.759+852A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606917 | ||||||
| chr8:58606960
|
A | G | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.759+809T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606960 | ||||||
| chr8:58606985
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.759+784A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58606985 | ||||||
| chr8:58607040
|
G | A | 1 | a0002c0002t0001g0220 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.759+729C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607040 | ||||||
| chr8:58607078
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 144 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.759+691T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607078 | ||||||
| chr8:58607108
|
T | C | 3 | a0001c0001t0001g0208a0003c0005t0001g0212a0003c0005t0009g0035 | 3 | HG03130.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.759+661A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607108 | ||||||
| chr8:58607161
|
A | G | 69 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0253others(66): Show | 75 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.759+608T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607161 | ||||||
| chr8:58607168
|
T | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.759+601A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607168 | ||||||
| chr8:58607169
|
C | G | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.759+600G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607169 | ||||||
| chr8:58607232
|
G | A | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.759+537C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607232 | ||||||
| chr8:58607415
|
C | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+354G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607415 | ||||||
| chr8:58607640
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.759+129T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607640 | ||||||
| chr8:58607688
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.759+81T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607688 | ||||||
| chr8:58607701
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | NA18955.hp1 NA18971.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.759+68C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607701 | ||||||
| chr8:58607751
|
A | C | 18 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(15): Show | 19 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.759+18T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 11/30 | chr8 | 58607751 | ||||||
| chr8:58607992
|
T | C | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.688-152A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58607992 | ||||||
| chr8:58608152
|
G | A | 83 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(80): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.688-312C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58608152 | ||||||
| chr8:58608524
|
G | T | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.688-684C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58608524 | ||||||
| chr8:58608698
|
G | A | 1 | a0001c0003t0001g0258 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.688-858C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58608698 | ||||||
| chr8:58608753
|
A | G | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.687+851T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58608753 | ||||||
| chr8:58609151
|
T | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0145a0001c0001t0001g0340others(2): Show | 5 | HG00408.hp2 NA18955.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+453A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609151 | ||||||
| chr8:58609296
|
C | G | 3 | a0001c0001t0001g0208a0003c0005t0001g0212a0003c0005t0009g0035 | 3 | HG03130.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.687+308G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609296 | ||||||
| chr8:58609322
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.687+282C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609322 | ||||||
| chr8:58609328
|
T | C | 2 | a0001c0001t0002g0256a0001c0001t0007g0030 | 2 | NA18747.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.687+276A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609328 | ||||||
| chr8:58609387
|
C | T | 5 | a0001c0001t0002g0181a0001c0001t0002g0255a0001c0001t0002g0301others(2): Show | 5 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+217G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609387 | ||||||
| chr8:58609412
|
C | G | 66 | a0001c0001t0001g0138a0001c0001t0001g0253a0001c0001t0008g0036others(63): Show | 72 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.687+192G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609412 | ||||||
| chr8:58609426
|
A | C | 1 | a0001c0001t0001g0323 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.687+178T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609426 | ||||||
| chr8:58609434
|
T | C | 1 | a0001c0003t0001g0300 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.687+170A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609434 | ||||||
| chr8:58609475
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 145 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.687+129G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 10/30 | chr8 | 58609475 | ||||||
| chr8:58609875
|
T | G | 1 | a0002c0002t0001g0327 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.558-142A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58609875 | ||||||
| chr8:58609918
|
A | T | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558-185T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58609918 | ||||||
| chr8:58609976
|
G | A | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.558-243C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58609976 | ||||||
| chr8:58610191
|
C | T | 88 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(85): Show | 95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-458G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610191 | ||||||
| chr8:58610347
|
A | G | 89 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(86): Show | 96 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.558-614T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610347 | ||||||
| chr8:58610578
|
C | T | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.558-845G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610578 | ||||||
| chr8:58610640
|
G | T | 1 | a0001c0001t0002g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.558-907C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610640 | ||||||
| chr8:58610673
|
C | A | 93 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(90): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-940G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610673 | ||||||
| chr8:58610707
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.558-974G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610707 | ||||||
| chr8:58610769
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0164 | 2 | NA18953.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.558-1036C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610769 | ||||||
| chr8:58610807
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.558-1074C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610807 | ||||||
| chr8:58610835
|
T | C | 88 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(85): Show | 95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-1102A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610835 | ||||||
| chr8:58610885
|
T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 145 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.558-1152A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610885 | ||||||
| chr8:58610893
|
A | T | 1 | a0001c0003t0001g0300 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.558-1160T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58610893 | ||||||
| chr8:58611031
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG01257.hp1 HG01258.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.558-1298G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611031 | ||||||
| chr8:58611232
|
T | C | 10 | a0001c0001t0001g0138a0001c0001t0001g0253a0001c0001t0008g0036others(7): Show | 10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.558-1499A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611232 | ||||||
| chr8:58611489
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.558-1756A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611489 | ||||||
| chr8:58611565
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.558-1832A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611565 | ||||||
| chr8:58611577
|
T | C | 88 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(85): Show | 95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-1844A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611577 | ||||||
| chr8:58611772
|
G | A | 5 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.558-2039C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611772 | ||||||
| chr8:58611871
|
G | A | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.558-2138C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611871 | ||||||
| chr8:58611978
|
T | C | 184 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(181): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.558-2245A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58611978 | ||||||
| chr8:58612325
|
G | T | 83 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(80): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.558-2592C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612325 | ||||||
| chr8:58612326
|
A | T | 83 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(80): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.558-2593T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612326 | ||||||
| chr8:58612355
|
G | A | 11 | a0002c0002t0001g0011a0002c0002t0001g0072a0002c0002t0001g0073others(8): Show | 13 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.558-2622C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612355 | ||||||
| chr8:58612386
|
G | C | 1 | a0002c0002t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.558-2653C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612386 | ||||||
| chr8:58612395
|
C | G | 1 | a0001c0001t0001g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.558-2662G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612395 | ||||||
| chr8:58612566
|
T | C | 88 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(85): Show | 95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-2833A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612566 | ||||||
| chr8:58612641
|
G | C | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.558-2908C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612641 | ||||||
| chr8:58612894
|
A | G | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558-3161T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612894 | ||||||
| chr8:58612963
|
T | G | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.558-3230A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58612963 | ||||||
| chr8:58613151
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.558-3418T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613151 | ||||||
| chr8:58613180
|
T | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 146 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.558-3447A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613180 | ||||||
| chr8:58613210
|
C | T | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.558-3477G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613210 | ||||||
| chr8:58613287
|
G | T | 2 | a0001c0001t0001g0192a0001c0003t0001g0211 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.558-3554C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613287 | ||||||
| chr8:58613520
|
G | T | 88 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(85): Show | 95 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.558-3787C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613520 | ||||||
| chr8:58613847
|
A | T | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.558-4114T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58613847 | ||||||
| chr8:58614106
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.558-4373A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614106 | ||||||
| chr8:58614140
|
C | T | 85 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0089others(82): Show | 87 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.558-4407G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614140 | ||||||
| chr8:58614479
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.558-4746G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614479 | ||||||
| chr8:58614513
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.558-4780C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614513 | ||||||
| chr8:58614577
|
C | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.558-4844G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614577 | ||||||
| chr8:58614640
|
C | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558-4907G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614640 | ||||||
| chr8:58614653
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.558-4920C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614653 | ||||||
| chr8:58614701
|
C | T | 1 | a0002c0002t0002g0264 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.558-4968G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614701 | ||||||
| chr8:58614769
|
G | A | 2 | a0001c0001t0008g0036a0001c0003t0001g0110 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.558-5036C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614769 | ||||||
| chr8:58614782
|
C | T | 1 | a0001c0003t0001g0339 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.558-5049G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58614782 | ||||||
| chr8:58615150
|
G | A | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(10): Show | 13 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.558-5417C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615150 | ||||||
| chr8:58615254
|
C | A | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.558-5521G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615254 | ||||||
| chr8:58615347
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.558-5614G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615347 | ||||||
| chr8:58615482
|
ACATATTC others(4): Show |
A | 2 | a0002c0002t0005g0005a0002c0002t0005g0019 | 3 | NA18961.hp1 NA18990.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.558-5760_558-5750d others(13): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615482 | ||||||
| chr8:58615588
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.558-5855G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615588 | ||||||
| chr8:58615686
|
A | T | 1 | a0001c0001t0002g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.558-5953T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615686 | ||||||
| chr8:58615753
|
C | G | 20 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(17): Show | 21 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.558-6020G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615753 | ||||||
| chr8:58615974
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.558-6241C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615974 | ||||||
| chr8:58615976
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.558-6243T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58615976 | ||||||
| chr8:58616047
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.558-6314C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616047 | ||||||
| chr8:58616224
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0003g0007a0001c0001t0003g0043others(1): Show | 5 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-6491G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616224 | ||||||
| chr8:58616452
|
G | GA | 5 | a0001c0001t0002g0191a0001c0001t0002g0329a0001c0001t0002g0330others(2): Show | 5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-6720dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616452 | ||||||
| chr8:58616701
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+6519T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616701 | ||||||
| chr8:58616704
|
T | A | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.557+6516A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616704 | ||||||
| chr8:58616874
|
A | G | 5 | a0001c0001t0002g0191a0001c0001t0002g0329a0001c0001t0002g0330others(2): Show | 5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.557+6346T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616874 | ||||||
| chr8:58616876
|
G | A | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.557+6344C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616876 | ||||||
| chr8:58616880
|
C | T | 5 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.557+6340G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616880 | ||||||
| chr8:58616985
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.557+6235T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616985 | ||||||
| chr8:58616988
|
T | C | 97 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(94): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.557+6232A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58616988 | ||||||
| chr8:58617087
|
T | C | 12 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(9): Show | 12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.557+6133A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617087 | ||||||
| chr8:58617379
|
C | A | 11 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0199others(8): Show | 11 | HG00408.hp1 HG00735.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.557+5841G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617379 | ||||||
| chr8:58617494
|
A | G | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.557+5726T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617494 | ||||||
| chr8:58617518
|
A | C | 2 | a0001c0001t0002g0214a0001c0004t0001g0116 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.557+5702T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617518 | ||||||
| chr8:58617608
|
A | G | 2 | a0001c0001t0002g0214a0001c0004t0001g0116 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.557+5612T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617608 | ||||||
| chr8:58617647
|
A | G | 2 | a0003c0005t0002g0207a0003c0005t0003g0044 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.557+5573T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617647 | ||||||
| chr8:58617994
|
A | T | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+5226T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58617994 | ||||||
| chr8:58618003
|
CCTTTGCA others(30): Show |
C | 1 | a0001c0001t0001g0083 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.557+5180_557+5216d others(39): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618003 | ||||||
| chr8:58618008
|
G | T | 2 | a0003c0005t0002g0207a0003c0005t0003g0044 | 2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.557+5212C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618008 | ||||||
| chr8:58618021
|
C | T | 4 | a0002c0002t0001g0011a0002c0002t0001g0221a0002c0002t0004g0006others(1): Show | 6 | NA18943.hp1 NA18945.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+5199G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618021 | ||||||
| chr8:58618216
|
T | G | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.557+5004A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618216 | ||||||
| chr8:58618348
|
A | G | 97 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(94): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.557+4872T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618348 | ||||||
| chr8:58618401
|
A | C | 1 | a0001c0001t0002g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.557+4819T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618401 | ||||||
| chr8:58618570
|
T | C | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.557+4650A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618570 | ||||||
| chr8:58618624
|
C | G | 99 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(96): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.557+4596G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618624 | ||||||
| chr8:58618815
|
C | T | 19 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(16): Show | 20 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.557+4405G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618815 | ||||||
| chr8:58618826
|
C | T | 2 | a0001c0001t0002g0214a0001c0004t0001g0116 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.557+4394G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618826 | ||||||
| chr8:58618846
|
G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.557+4374C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618846 | ||||||
| chr8:58618909
|
C | T | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.557+4311G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618909 | ||||||
| chr8:58618972
|
C | G | 97 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(94): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.557+4248G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58618972 | ||||||
| chr8:58619061
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0194 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.557+4159C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619061 | ||||||
| chr8:58619082
|
C | A | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.557+4138G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619082 | ||||||
| chr8:58619308
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+3912C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619308 | ||||||
| chr8:58619335
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+3885A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619335 | ||||||
| chr8:58619389
|
G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.557+3831C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619389 | ||||||
| chr8:58619641
|
C | A | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.557+3579G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619641 | ||||||
| chr8:58619691
|
T | A | 1 | a0001c0003t0001g0298 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.557+3529A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619691 | ||||||
| chr8:58619709
|
A | G | 1 | a0006c0007t0001g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.557+3511T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619709 | ||||||
| chr8:58619858
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.557+3362T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619858 | ||||||
| chr8:58619922
|
G | A | 1 | a0001c0001t0006g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.557+3298C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619922 | ||||||
| chr8:58619927
|
T | C | 2 | a0001c0009t0001g0251a0001c0009t0001g0252 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.557+3293A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619927 | ||||||
| chr8:58619986
|
G | A | 99 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(96): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.557+3234C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58619986 | ||||||
| chr8:58620022
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.557+3198C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620022 | ||||||
| chr8:58620079
|
A | C | 1 | a0001c0001t0003g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.557+3141T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620079 | ||||||
| chr8:58620148
|
G | T | 97 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(94): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.557+3072C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620148 | ||||||
| chr8:58620228
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0241others(2): Show | 8 | NA18943.hp2 NA18947.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.557+2992T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620228 | ||||||
| chr8:58620410
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.557+2810G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620410 | ||||||
| chr8:58620467
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG00642.hp1 HG01123.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.557+2753A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620467 | ||||||
| chr8:58620486
|
A | T | 2 | a0001c0003t0001g0107a0001c0003t0001g0117 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.557+2734T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620486 | ||||||
| chr8:58620501
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0155a0001c0001t0001g0283 | 3 | NA18951.hp1 NA19070.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.557+2719C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620501 | ||||||
| chr8:58620958
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.557+2262A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58620958 | ||||||
| chr8:58621147
|
C | T | 2 | a0001c0004t0001g0202a0001c0004t0001g0210 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.557+2073G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621147 | ||||||
| chr8:58621148
|
G | A | 3 | a0001c0001t0011g0039a0006c0007t0001g0103a0006c0007t0003g0038 | 3 | HG02970.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.557+2072C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621148 | ||||||
| chr8:58621237
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.557+1983T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621237 | ||||||
| chr8:58621501
|
A | G | 99 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(96): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.557+1719T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621501 | ||||||
| chr8:58621783
|
T | C | 98 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(95): Show | 103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.557+1437A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621783 | ||||||
| chr8:58621844
|
T | C | 1 | a0001c0001t0006g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.557+1376A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621844 | ||||||
| chr8:58621978
|
T | G | 100 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(97): Show | 105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.557+1242A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58621978 | ||||||
| chr8:58622231
|
C | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+989G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58622231 | ||||||
| chr8:58622636
|
G | T | 5 | a0001c0001t0002g0191a0001c0001t0002g0329a0001c0001t0002g0330others(2): Show | 5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.557+584C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58622636 | ||||||
| chr8:58622843
|
A | G | 1 | a0001c0003t0001g0056 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.557+377T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58622843 | ||||||
| chr8:58622915
|
G | T | 1 | a0001c0001t0008g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.557+305C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58622915 | ||||||
| chr8:58623063
|
G | C | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.557+157C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 9/30 | chr8 | 58623063 | ||||||
| chr8:58623300
|
A | ACG | 103 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(100): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.505-29_505-28insCG | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 8/30 | chr8 | 58623300 | ||||||
| chr8:58623301
|
T | A | 103 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(100): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.505-29A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 8/30 | chr8 | 58623301 | ||||||
| chr8:58623302
|
T | A | 103 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(100): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.505-30A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 8/30 | chr8 | 58623302 | ||||||
| chr8:58623467
|
A | G | 1 | a0001c0001t0002g0146 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.457-43T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 7/30 | chr8 | 58623467 | ||||||
| chr8:58623552
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.457-128A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 7/30 | chr8 | 58623552 | ||||||
| chr8:58623563
|
T | C | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.457-139A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 7/30 | chr8 | 58623563 | ||||||
| chr8:58623613
|
A | G | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.456+96T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 7/30 | chr8 | 58623613 | ||||||
| chr8:58624035
|
A | AT | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.385-256dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | ||||||
| chr8:58624035
|
A | ATT | 18 | a0001c0001t0001g0080a0001c0001t0001g0123a0001c0001t0001g0166others(15): Show | 18 | HG00673.hp2 HG00738.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.385-257_385-256dup others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | ||||||
| chr8:58624035
|
AT | A | 74 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0136others(71): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.385-256delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | ||||||
| chr8:58624035
|
ATT | A | 87 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(84): Show | 92 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.385-257_385-256del others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | ||||||
| chr8:58624035
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.385-269_385-256del others(14): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624035 | ||||||
| chr8:58624222
|
A | G | 6 | a0002c0002t0001g0072a0002c0002t0001g0073a0002c0002t0001g0075others(3): Show | 6 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-442T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624222 | ||||||
| chr8:58624235
|
C | T | 1 | a0002c0002t0001g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.385-455G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624235 | ||||||
| chr8:58624299
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-519C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624299 | ||||||
| chr8:58624316
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.385-536C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624316 | ||||||
| chr8:58624483
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.385-703A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624483 | ||||||
| chr8:58624738
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.385-958G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624738 | ||||||
| chr8:58624859
|
T | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-1079A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624859 | ||||||
| chr8:58624873
|
T | G | 4 | a0001c0001t0003g0008a0001c0001t0003g0046a0001c0001t0003g0047others(1): Show | 5 | HG02258.hp2 HG02451.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-1093A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624873 | ||||||
| chr8:58624893
|
T | C | 1 | a0001c0001t0008g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.385-1113A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624893 | ||||||
| chr8:58624895
|
T | C | 2 | a0001c0001t0002g0088a0001c0001t0002g0092 | 2 | NA18970.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.385-1115A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624895 | ||||||
| chr8:58624903
|
C | T | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385-1123G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58624903 | ||||||
| chr8:58625088
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-1308G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625088 | ||||||
| chr8:58625277
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.385-1497G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625277 | ||||||
| chr8:58625386
|
G | T | 12 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(9): Show | 12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.385-1606C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625386 | ||||||
| chr8:58625393
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.385-1613G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625393 | ||||||
| chr8:58625394
|
A | ATATATAT others(9): Show |
1 | a0004c0006t0002g0345 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.385-1615_385-1614i others(18): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625394
|
A | ATATATAT others(13): Show |
14 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.385-1615_385-1614i others(22): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625394
|
A | ATATATAT others(17): Show |
71 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0093others(68): Show | 76 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.385-1615_385-1614i others(26): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625394
|
A | ATATATAT others(21): Show |
11 | a0001c0001t0001g0089a0001c0001t0001g0188a0001c0001t0001g0189others(8): Show | 11 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-1615_385-1614i others(30): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625394
|
A | ATATGTAT others(9): Show |
1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-1630_385-1615d others(18): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625394
|
A | ATATGTAT others(13): Show |
1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.385-1634_385-1615d others(22): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625394
|
A | ATATGTAT others(17): Show |
1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.385-1615_385-1614i others(26): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625394
|
A | ATGTATGT others(11): Show |
1 | a0001c0001t0002g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.385-1615_385-1614i others(20): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625394
|
ATATG | A | 10 | a0001c0001t0001g0138a0001c0001t0001g0253a0001c0001t0008g0036others(7): Show | 10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-1618_385-1615d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625394 | ||||||
| chr8:58625415
|
T | C | 1 | a0002c0002t0001g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.385-1635A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625415 | ||||||
| chr8:58625418
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01167.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.385-1638T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625418 | ||||||
| chr8:58625423
|
T | C | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-1643A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625423 | ||||||
| chr8:58625448
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.385-1668G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625448 | ||||||
| chr8:58625511
|
T | C | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.385-1731A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625511 | ||||||
| chr8:58625519
|
C | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-1739G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625519 | ||||||
| chr8:58625519
|
C | T | 2 | a0001c0001t0002g0133a0001c0001t0002g0206 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.385-1739G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625519 | ||||||
| chr8:58625614
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-1834C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625614 | ||||||
| chr8:58625636
|
T | C | 2 | a0002c0002t0004g0025a0002c0002t0004g0026 | 2 | HG02080.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.385-1856A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625636 | ||||||
| chr8:58625677
|
C | T | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-1897G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625677 | ||||||
| chr8:58625691
|
T | C | 101 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(98): Show | 106 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.385-1911A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625691 | ||||||
| chr8:58625755
|
G | T | 3 | a0001c0001t0001g0104a0001c0001t0003g0007a0001c0001t0003g0043 | 4 | HG02109.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-1975C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625755 | ||||||
| chr8:58625802
|
G | T | 1 | a0001c0003t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.385-2022C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625802 | ||||||
| chr8:58625813
|
A | G | 27 | a0001c0001t0001g0192a0001c0003t0001g0010a0001c0003t0001g0012others(24): Show | 29 | HG00099.hp2 HG00609.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.385-2033T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625813 | ||||||
| chr8:58625916
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.385-2136T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625916 | ||||||
| chr8:58625930
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-2150A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625930 | ||||||
| chr8:58625986
|
G | T | 1 | a0001c0001t0001g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.385-2206C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58625986 | ||||||
| chr8:58626041
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.385-2261T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626041 | ||||||
| chr8:58626091
|
C | CT | 17 | a0001c0001t0001g0153a0001c0001t0001g0157a0001c0001t0001g0208others(14): Show | 17 | HG01934.hp1 HG02071.hp1 HG03453.hp1 others(14): Show |
intron_variant | MODIFIER | c.385-2312dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626091 | ||||||
| chr8:58626091
|
C | CTT | 27 | a0001c0001t0001g0192a0001c0003t0001g0010a0001c0003t0001g0012others(24): Show | 29 | HG00099.hp2 HG00609.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.385-2313_385-2312d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626091 | ||||||
| chr8:58626091
|
CT | C | 87 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(84): Show | 92 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.385-2312delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626091 | ||||||
| chr8:58626092
|
T | G | 17 | a0001c0001t0001g0057a0001c0001t0001g0093a0001c0001t0001g0134others(14): Show | 17 | HG02486.hp1 HG02572.hp2 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.385-2312A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626092 | ||||||
| chr8:58626093
|
T | G | 81 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(78): Show | 86 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.385-2313A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626093 | ||||||
| chr8:58626094
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.385-2314A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626094 | ||||||
| chr8:58626159
|
C | T | 2 | a0001c0001t0002g0330a0001c0001t0002g0332 | 2 | NA18994.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.385-2379G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626159 | ||||||
| chr8:58626160
|
G | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-2380C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626160 | ||||||
| chr8:58626161
|
C | T | 102 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(99): Show | 107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.385-2381G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626161 | ||||||
| chr8:58626256
|
C | T | 67 | a0001c0001t0001g0069a0001c0001t0001g0138a0001c0001t0001g0149others(64): Show | 70 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.385-2476G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626256 | ||||||
| chr8:58626286
|
A | AG | 5 | a0001c0001t0001g0208a0001c0004t0001g0116a0003c0005t0003g0044others(2): Show | 5 | HG02572.hp1 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-2507dupC | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626286 | ||||||
| chr8:58626287
|
G | GC | 100 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(97): Show | 105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.385-2508_385-2507i others(3): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626287 | ||||||
| chr8:58626374
|
A | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-2594T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626374 | ||||||
| chr8:58626583
|
T | C | 102 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(99): Show | 107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.385-2803A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626583 | ||||||
| chr8:58626600
|
A | T | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-2820T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626600 | ||||||
| chr8:58626645
|
T | A | 17 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0124others(14): Show | 18 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.385-2865A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626645 | ||||||
| chr8:58626673
|
T | A | 12 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(9): Show | 12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.385-2893A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626673 | ||||||
| chr8:58626837
|
T | C | 1 | a0001c0001t0002g0332 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.385-3057A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626837 | ||||||
| chr8:58626866
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0321a0002c0002t0001g0151 | 4 | HG00099.hp1 HG00741.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-3086C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58626866 | ||||||
| chr8:58627059
|
G | C | 9 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(6): Show | 9 | HG01069.hp1 HG01192.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.385-3279C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627059 | ||||||
| chr8:58627173
|
G | T | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.385-3393C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627173 | ||||||
| chr8:58627287
|
G | A | 1 | a0001c0004t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.385-3507C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627287 | ||||||
| chr8:58627321
|
C | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.385-3541G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627321 | ||||||
| chr8:58627324
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.385-3544A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627324 | ||||||
| chr8:58627555
|
T | C | 100 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(97): Show | 105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.385-3775A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627555 | ||||||
| chr8:58627592
|
A | G | 1 | a0001c0003t0001g0341 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.385-3812T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627592 | ||||||
| chr8:58627610
|
C | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.385-3830G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627610 | ||||||
| chr8:58627635
|
T | G | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385-3855A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627635 | ||||||
| chr8:58627687
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.384+3809T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627687 | ||||||
| chr8:58627884
|
A | G | 1 | a0001c0001t0011g0039 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.384+3612T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58627884 | ||||||
| chr8:58628020
|
G | A | 217 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(214): Show | 228 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.384+3476C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628020 | ||||||
| chr8:58628090
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.384+3406A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628090 | ||||||
| chr8:58628200
|
T | C | 3 | a0001c0001t0011g0039a0006c0007t0001g0103a0006c0007t0003g0038 | 3 | HG02970.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.384+3296A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628200 | ||||||
| chr8:58628272
|
C | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.384+3224G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628272 | ||||||
| chr8:58628431
|
C | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0171a0001c0001t0001g0286others(4): Show | 8 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+3065G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628431 | ||||||
| chr8:58628499
|
A | G | 2 | a0002c0002t0001g0061a0002c0002t0001g0062 | 2 | NA18963.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.384+2997T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628499 | ||||||
| chr8:58628827
|
A | G | 220 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(217): Show | 231 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.384+2669T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628827 | ||||||
| chr8:58628995
|
G | A | 1 | a0001c0003t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.384+2501C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58628995 | ||||||
| chr8:58629409
|
CTCTT | C | 86 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0089others(83): Show | 91 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.384+2083_384+2086d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58629409 | ||||||
| chr8:58629457
|
A | G | 53 | a0001c0001t0001g0069a0001c0001t0001g0149a0001c0001t0001g0150others(50): Show | 56 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.384+2039T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58629457 | ||||||
| chr8:58629558
|
A | G | 2 | a0002c0002t0001g0058a0002c0002t0001g0060 | 2 | NA18959.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.384+1938T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58629558 | ||||||
| chr8:58629622
|
AAAC | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(342): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.384+1871_384+1873d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58629622 | ||||||
| chr8:58630014
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.384+1482G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630014 | ||||||
| chr8:58630098
|
G | A | 12 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(9): Show | 12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.384+1398C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630098 | ||||||
| chr8:58630142
|
C | T | 95 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(92): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.384+1354G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630142 | ||||||
| chr8:58630173
|
G | A | 3 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252 | 3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.384+1323C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630173 | ||||||
| chr8:58630321
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+1175A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630321 | ||||||
| chr8:58630363
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0233 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.384+1133A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630363 | ||||||
| chr8:58630380
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+1116A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630380 | ||||||
| chr8:58630398
|
T | G | 1 | a0001c0001t0001g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.384+1098A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630398 | ||||||
| chr8:58630600
|
G | T | 1 | a0001c0001t0001g0343 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.384+896C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630600 | ||||||
| chr8:58630741
|
A | G | 97 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(94): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.384+755T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630741 | ||||||
| chr8:58630839
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+657C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630839 | ||||||
| chr8:58630970
|
G | C | 5 | a0001c0001t0001g0208a0001c0004t0001g0116a0003c0005t0003g0044others(2): Show | 5 | HG02572.hp1 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+526C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58630970 | ||||||
| chr8:58631031
|
G | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.384+465C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58631031 | ||||||
| chr8:58631273
|
G | GT | 6 | a0001c0001t0001g0104a0001c0001t0001g0171a0001c0001t0001g0262others(3): Show | 7 | HG00735.hp2 HG02109.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+222dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58631273 | ||||||
| chr8:58631313
|
A | C | 1 | a0002c0002t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.384+183T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58631313 | ||||||
| chr8:58631347
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0246 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.384+149G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 6/30 | chr8 | 58631347 | ||||||
| chr8:58631628
|
A | C | 12 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(9): Show | 12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-82T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631628 | ||||||
| chr8:58631693
|
A | T | 86 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0089others(83): Show | 91 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-147T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631693 | ||||||
| chr8:58631777
|
T | A | 1 | a0001c0003t0003g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-231A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631777 | ||||||
| chr8:58631852
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.334-306C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631852 | ||||||
| chr8:58631854
|
G | A | 86 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0089others(83): Show | 91 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-308C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631854 | ||||||
| chr8:58631870
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0233 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.334-324C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631870 | ||||||
| chr8:58631995
|
T | C | 3 | a0001c0001t0011g0039a0006c0007t0001g0103a0006c0007t0003g0038 | 3 | HG02970.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.334-449A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58631995 | ||||||
| chr8:58632001
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.334-455T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632001 | ||||||
| chr8:58632450
|
C | T | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.334-904G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632450 | ||||||
| chr8:58632503
|
A | T | 96 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(93): Show | 101 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.334-957T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632503 | ||||||
| chr8:58632569
|
G | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1023C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632569 | ||||||
| chr8:58632795
|
A | G | 103 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(100): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.334-1249T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632795 | ||||||
| chr8:58632819
|
T | A | 5 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(2): Show | 5 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-1273A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58632819 | ||||||
| chr8:58633008
|
T | C | 1 | a0002c0002t0001g0058 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.334-1462A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633008 | ||||||
| chr8:58633019
|
C | T | 95 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(92): Show | 100 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.334-1473G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633019 | ||||||
| chr8:58633187
|
C | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.334-1641G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633187 | ||||||
| chr8:58633189
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0208 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.334-1643G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633189 | ||||||
| chr8:58633190
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.334-1644C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633190 | ||||||
| chr8:58633199
|
G | T | 1 | a0002c0002t0001g0195 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.334-1653C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633199 | ||||||
| chr8:58633202
|
C | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.334-1656G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633202 | ||||||
| chr8:58633622
|
G | A | 1 | a0002c0013t0001g0197 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.333+1567C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633622 | ||||||
| chr8:58633906
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0208 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.333+1283T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633906 | ||||||
| chr8:58633985
|
A | T | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+1204T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633985 | ||||||
| chr8:58633987
|
A | G | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+1202T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58633987 | ||||||
| chr8:58634011
|
T | C | 217 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(214): Show | 228 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.333+1178A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634011 | ||||||
| chr8:58634031
|
T | C | 1 | a0001c0003t0001g0300 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.333+1158A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634031 | ||||||
| chr8:58634076
|
T | C | 1 | a0006c0007t0001g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.333+1113A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634076 | ||||||
| chr8:58634124
|
C | T | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.333+1065G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634124 | ||||||
| chr8:58634226
|
A | G | 1 | a0001c0003t0001g0298 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.333+963T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634226 | ||||||
| chr8:58634367
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0241others(3): Show | 9 | NA18943.hp2 NA18947.hp2 NA18974.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+822G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634367 | ||||||
| chr8:58634379
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.333+810G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634379 | ||||||
| chr8:58634516
|
A | G | 27 | a0001c0001t0001g0192a0001c0003t0001g0010a0001c0003t0001g0012others(24): Show | 29 | HG00099.hp2 HG00609.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.333+673T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634516 | ||||||
| chr8:58634601
|
C | A | 1 | a0001c0001t0002g0146 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.333+588G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634601 | ||||||
| chr8:58634658
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.333+531T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634658 | ||||||
| chr8:58634941
|
G | A | 7 | a0001c0001t0001g0312a0001c0001t0002g0156a0001c0001t0002g0215others(4): Show | 7 | NA18951.hp2 NA18952.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+248C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 5/30 | chr8 | 58634941 | ||||||
| chr8:58635240
|
A | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.297-15T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 4/30 | chr8 | 58635240 | ||||||
| chr8:58635243
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0287a0008c0012t0001g0294 | 3 | HG02735.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.297-18C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 4/30 | chr8 | 58635243 | ||||||
| chr8:58635245
|
C | A | 85 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0089others(82): Show | 90 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.297-20G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 4/30 | chr8 | 58635245 | ||||||
| chr8:58635551
|
G | A | 26 | a0001c0001t0001g0192a0001c0003t0001g0010a0001c0003t0001g0012others(23): Show | 28 | HG00099.hp2 HG00609.hp1 HG01123.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.150-5C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635551 | ||||||
| chr8:58635709
|
A | G | 16 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(13): Show | 17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-163T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635709 | ||||||
| chr8:58635742
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.150-196G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635742 | ||||||
| chr8:58635875
|
G | A | 26 | a0001c0001t0001g0192a0001c0003t0001g0010a0001c0003t0001g0012others(23): Show | 28 | HG00099.hp2 HG00609.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.150-329C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635875 | ||||||
| chr8:58635930
|
A | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0084a0001c0001t0001g0119others(23): Show | 28 | HG00438.hp2 HG00609.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.150-384T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635930 | ||||||
| chr8:58635943
|
T | C | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.150-397A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635943 | ||||||
| chr8:58635973
|
C | T | 6 | a0001c0001t0002g0249a0001c0001t0002g0303a0001c0001t0002g0304others(3): Show | 6 | HG00323.hp1 HG00738.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-427G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58635973 | ||||||
| chr8:58636085
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0208a0005c0015t0009g0034others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-539A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636085 | ||||||
| chr8:58636209
|
A | G | 1 | a0002c0002t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.150-663T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636209 | ||||||
| chr8:58636246
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.150-700G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636246 | ||||||
| chr8:58636257
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.150-711G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636257 | ||||||
| chr8:58636353
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-807T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636353 | ||||||
| chr8:58636386
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-840A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636386 | ||||||
| chr8:58636433
|
G | C | 86 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0089others(83): Show | 91 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.150-887C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636433 | ||||||
| chr8:58636694
|
T | G | 58 | a0001c0001t0001g0069a0001c0001t0001g0149a0001c0001t0001g0150others(55): Show | 61 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.150-1148A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636694 | ||||||
| chr8:58636712
|
C | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-1166G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636712 | ||||||
| chr8:58636736
|
A | G | 3 | a0001c0001t0002g0098a0001c0001t0002g0114a0001c0001t0002g0186 | 3 | HG02559.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150-1190T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636736 | ||||||
| chr8:58636740
|
C | G | 1 | a0001c0001t0002g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.150-1194G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636740 | ||||||
| chr8:58636784
|
C | G | 99 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(96): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.150-1238G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636784 | ||||||
| chr8:58636945
|
A | G | 1 | a0001c0001t0006g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.150-1399T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58636945 | ||||||
| chr8:58637017
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.150-1485_150-1472d others(16): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637017 | ||||||
| chr8:58637017
|
TACAC | T | 203 | a0001c0001t0001g0016a0001c0001t0001g0057a0001c0001t0001g0069others(200): Show | 214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.150-1475_150-1472d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637017 | ||||||
| chr8:58637038
|
ACACC | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(3): Show | 6 | HG01109.hp1 HG01192.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-1496_150-1493d others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637038 | ||||||
| chr8:58637040
|
A | C | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.150-1494T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637040 | ||||||
| chr8:58637042
|
C | A | 7 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0001t0001g0274others(4): Show | 7 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-1496G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637042 | ||||||
| chr8:58637102
|
C | T | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.150-1556G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637102 | ||||||
| chr8:58637233
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0171a0001c0001t0001g0286others(2): Show | 6 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-1687G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637233 | ||||||
| chr8:58637288
|
T | C | 1 | a0006c0007t0003g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150-1742A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637288 | ||||||
| chr8:58637373
|
C | A | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.150-1827G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637373 | ||||||
| chr8:58637528
|
C | G | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.150-1982G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637528 | ||||||
| chr8:58637608
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-2062A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637608 | ||||||
| chr8:58637718
|
A | C | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.150-2172T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637718 | ||||||
| chr8:58637836
|
G | A | 1 | a0001c0003t0001g0137 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-2290C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637836 | ||||||
| chr8:58637962
|
AATCCCAA others(4): Show |
A | 7 | a0002c0002t0001g0072a0002c0002t0001g0073a0002c0002t0001g0075others(4): Show | 7 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-2427_150-2417d others(13): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58637962 | ||||||
| chr8:58638012
|
T | C | 100 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(97): Show | 105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.150-2466A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638012 | ||||||
| chr8:58638057
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0208 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.150-2511A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638057 | ||||||
| chr8:58638307
|
G | A | 1 | a0001c0008t0002g0316 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.150-2761C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638307 | ||||||
| chr8:58638341
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.150-2795C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638341 | ||||||
| chr8:58638457
|
TG | T | 16 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(13): Show | 17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-2912delC | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638457 | ||||||
| chr8:58638508
|
G | A | 68 | a0001c0001t0001g0069a0001c0001t0001g0138a0001c0001t0001g0149others(65): Show | 71 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.150-2962C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638508 | ||||||
| chr8:58638575
|
C | T | 16 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(13): Show | 17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-3029G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638575 | ||||||
| chr8:58638620
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-3074T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638620 | ||||||
| chr8:58638702
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-3156G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638702 | ||||||
| chr8:58638910
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.150-3364C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58638910 | ||||||
| chr8:58639083
|
C | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-3537G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639083 | ||||||
| chr8:58639152
|
G | T | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.150-3606C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639152 | ||||||
| chr8:58639227
|
T | C | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.150-3681A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639227 | ||||||
| chr8:58639248
|
C | T | 1 | a0001c0001t0003g0008 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.150-3702G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639248 | ||||||
| chr8:58639278
|
C | T | 26 | a0001c0001t0001g0192a0001c0003t0001g0010a0001c0003t0001g0012others(23): Show | 28 | HG00099.hp2 HG00609.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.149+3706G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639278 | ||||||
| chr8:58639286
|
TA | T | 10 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(7): Show | 10 | HG01069.hp1 HG01192.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+3697delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639286 | ||||||
| chr8:58639297
|
A | G | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.149+3687T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639297 | ||||||
| chr8:58639297
|
AAAG | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0054others(110): Show | 120 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.149+3684_149+3686d others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639297 | ||||||
| chr8:58639300
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0208 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.149+3684C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639300 | ||||||
| chr8:58639325
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.149+3659A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639325 | ||||||
| chr8:58639355
|
C | A | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.149+3629G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639355 | ||||||
| chr8:58639722
|
T | G | 230 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(227): Show | 241 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.149+3262A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639722 | ||||||
| chr8:58639810
|
C | T | 1 | a0001c0001t0002g0329 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.149+3174G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639810 | ||||||
| chr8:58639875
|
A | G | 1 | a0002c0002t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.149+3109T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639875 | ||||||
| chr8:58639917
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+3067G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639917 | ||||||
| chr8:58639918
|
G | A | 5 | a0001c0001t0002g0191a0001c0001t0002g0329a0001c0001t0002g0330others(2): Show | 5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+3066C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639918 | ||||||
| chr8:58639958
|
T | C | 1 | a0001c0010t0006g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.149+3026A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58639958 | ||||||
| chr8:58640236
|
A | T | 3 | a0001c0001t0002g0214a0001c0001t0003g0007a0001c0001t0003g0043 | 4 | HG02109.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+2748T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640236 | ||||||
| chr8:58640336
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.149+2648A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640336 | ||||||
| chr8:58640555
|
GA | G | 102 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(99): Show | 107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.149+2428delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640555 | ||||||
| chr8:58640592
|
C | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+2392G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640592 | ||||||
| chr8:58640671
|
G | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.149+2313C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640671 | ||||||
| chr8:58640868
|
G | T | 58 | a0001c0001t0001g0069a0001c0001t0001g0149a0001c0001t0001g0150others(55): Show | 61 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.149+2116C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640868 | ||||||
| chr8:58640930
|
A | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0194 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+2054T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58640930 | ||||||
| chr8:58641109
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0246 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+1875G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641109 | ||||||
| chr8:58641387
|
A | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1597T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641387 | ||||||
| chr8:58641415
|
C | T | 2 | a0001c0009t0001g0251a0001c0009t0001g0252 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.149+1569G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641415 | ||||||
| chr8:58641470
|
CAT | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1512_149+1513d others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641470 | ||||||
| chr8:58641533
|
G | A | 2 | a0001c0008t0002g0315a0001c0008t0002g0316 | 2 | HG01993.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.149+1451C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641533 | ||||||
| chr8:58641534
|
C | A | 2 | a0001c0008t0002g0315a0001c0008t0002g0316 | 2 | HG01993.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.149+1450G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641534 | ||||||
| chr8:58641616
|
T | C | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.149+1368A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641616 | ||||||
| chr8:58641665
|
G | C | 12 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(9): Show | 12 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.149+1319C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641665 | ||||||
| chr8:58641849
|
C | T | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.149+1135G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641849 | ||||||
| chr8:58641894
|
C | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.149+1090G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58641894 | ||||||
| chr8:58642147
|
A | G | 94 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(91): Show | 99 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.149+837T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642147 | ||||||
| chr8:58642210
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+774C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642210 | ||||||
| chr8:58642217
|
T | A | 1 | a0001c0001t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149+767A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642217 | ||||||
| chr8:58642442
|
T | C | 2 | a0001c0001t0002g0318a0001c0001t0002g0319 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.149+542A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642442 | ||||||
| chr8:58642482
|
G | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.149+502C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642482 | ||||||
| chr8:58642571
|
C | A | 68 | a0001c0001t0001g0069a0001c0001t0001g0138a0001c0001t0001g0149others(65): Show | 71 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.149+413G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642571 | ||||||
| chr8:58642708
|
A | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+276T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642708 | ||||||
| chr8:58642766
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.149+218T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 2/30 | chr8 | 58642766 | ||||||
| chr8:58643086
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.60-13G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643086 | ||||||
| chr8:58643087
|
G | A | 1 | a0001c0001t0002g0338 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.60-14C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643087 | ||||||
| chr8:58643097
|
C | T | 73 | a0001c0001t0001g0069a0001c0001t0001g0138a0001c0001t0001g0149others(70): Show | 76 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.60-24G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643097 | ||||||
| chr8:58643172
|
T | A | 103 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(100): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.60-99A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643172 | ||||||
| chr8:58643232
|
T | C | 1 | a0001c0001t0002g0320 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.60-159A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643232 | ||||||
| chr8:58643306
|
T | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0324a0001c0001t0001g0325others(1): Show | 4 | HG00642.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-233A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643306 | ||||||
| chr8:58643435
|
G | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-362C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643435 | ||||||
| chr8:58643481
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-408G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643481 | ||||||
| chr8:58643486
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.60-413A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643486 | ||||||
| chr8:58643534
|
CT | C | 197 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(194): Show | 207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.60-462delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643534 | ||||||
| chr8:58643549
|
T | G | 4 | a0001c0001t0001g0182a0001c0009t0001g0251a0001c0009t0001g0252others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-476A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643549 | ||||||
| chr8:58643554
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.60-481G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643554 | ||||||
| chr8:58643597
|
G | A | 101 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(98): Show | 106 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.60-524C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643597 | ||||||
| chr8:58643625
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.60-552C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643625 | ||||||
| chr8:58643725
|
T | A | 1 | a0002c0002t0001g0073 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.60-652A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643725 | ||||||
| chr8:58643767
|
G | A | 11 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0199others(8): Show | 11 | HG00408.hp1 HG00735.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.60-694C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643767 | ||||||
| chr8:58643820
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-747G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643820 | ||||||
| chr8:58643851
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-778A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643851 | ||||||
| chr8:58643921
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.60-848C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643921 | ||||||
| chr8:58643923
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.60-850C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58643923 | ||||||
| chr8:58644434
|
C | T | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.60-1361G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644434 | ||||||
| chr8:58644474
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1401T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644474 | ||||||
| chr8:58644479
|
C | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1406G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644479 | ||||||
| chr8:58644655
|
A | C | 105 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(102): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.60-1582T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644655 | ||||||
| chr8:58644670
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1597C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644670 | ||||||
| chr8:58644677
|
G | A | 3 | a0001c0001t0011g0039a0006c0007t0001g0103a0006c0007t0003g0038 | 3 | HG02970.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.60-1604C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644677 | ||||||
| chr8:58644703
|
T | C | 54 | a0001c0001t0001g0069a0001c0001t0001g0149a0001c0001t0001g0150others(51): Show | 57 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.60-1630A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644703 | ||||||
| chr8:58644820
|
A | G | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-1747T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644820 | ||||||
| chr8:58644936
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1863A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644936 | ||||||
| chr8:58644964
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0069a0001c0001t0001g0097others(75): Show | 84 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.60-1891C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644964 | ||||||
| chr8:58644979
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1906T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58644979 | ||||||
| chr8:58645004
|
C | T | 16 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(13): Show | 17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.60-1931G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645004 | ||||||
| chr8:58645112
|
T | C | 1 | a0006c0007t0001g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.60-2039A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645112 | ||||||
| chr8:58645113
|
TA | T | 15 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0125others(12): Show | 16 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-2041delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645113 | ||||||
| chr8:58645204
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2131T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645204 | ||||||
| chr8:58645266
|
T | TA | 99 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(96): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.60-2194dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645266 | ||||||
| chr8:58645367
|
T | A | 1 | a0001c0001t0002g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.60-2294A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645367 | ||||||
| chr8:58645380
|
G | A | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.60-2307C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645380 | ||||||
| chr8:58645460
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2387G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645460 | ||||||
| chr8:58645468
|
G | C | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-2395C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645468 | ||||||
| chr8:58645696
|
T | C | 1 | a0001c0001t0002g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.60-2623A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645696 | ||||||
| chr8:58645697
|
C | G | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-2624G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645697 | ||||||
| chr8:58645766
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2693G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645766 | ||||||
| chr8:58645788
|
C | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0125others(6): Show | 10 | HG00597.hp2 NA18977.hp2 NA19000.hp2 others(7): Show |
intron_variant | MODIFIER | c.60-2715G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645788 | ||||||
| chr8:58645838
|
C | T | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-2765G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645838 | ||||||
| chr8:58645859
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.60-2786C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645859 | ||||||
| chr8:58645910
|
G | A | 69 | a0001c0001t0001g0069a0001c0001t0001g0138a0001c0001t0001g0149others(66): Show | 72 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.60-2837C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645910 | ||||||
| chr8:58645972
|
T | C | 12 | a0001c0001t0001g0104a0001c0001t0001g0182a0001c0001t0001g0208others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.60-2899A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645972 | ||||||
| chr8:58645985
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.60-2912C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58645985 | ||||||
| chr8:58646001
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2928T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646001 | ||||||
| chr8:58646016
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-2943T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646016 | ||||||
| chr8:58646035
|
C | G | 60 | a0001c0001t0001g0069a0001c0001t0001g0149a0001c0001t0001g0150others(57): Show | 63 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.60-2962G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646035 | ||||||
| chr8:58646044
|
A | AATC | 8 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0001t0001g0295others(5): Show | 8 | HG01433.hp2 HG01515.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-2974_60-2972dup others(3): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646044 | ||||||
| chr8:58646390
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-3317A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646390 | ||||||
| chr8:58646531
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0208 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.60-3458A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646531 | ||||||
| chr8:58646561
|
A | T | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.60-3488T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646561 | ||||||
| chr8:58646670
|
T | C | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-3597A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646670 | ||||||
| chr8:58646803
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.60-3730C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646803 | ||||||
| chr8:58646840
|
C | T | 17 | a0001c0001t0001g0089a0001c0001t0001g0145a0001c0001t0001g0340others(14): Show | 17 | HG00408.hp2 HG00673.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.60-3767G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646840 | ||||||
| chr8:58646993
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-3920A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58646993 | ||||||
| chr8:58647359
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-4286T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647359 | ||||||
| chr8:58647440
|
G | C | 16 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(13): Show | 17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.60-4367C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647440 | ||||||
| chr8:58647501
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.60-4428T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647501 | ||||||
| chr8:58647503
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.60-4430C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647503 | ||||||
| chr8:58647524
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.60-4451C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647524 | ||||||
| chr8:58647534
|
G | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0208a0005c0015t0009g0034others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-4461C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647534 | ||||||
| chr8:58647542
|
G | C | 16 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(13): Show | 17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.60-4469C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647542 | ||||||
| chr8:58647556
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-4483T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647556 | ||||||
| chr8:58647594
|
CA | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-4522delT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647594 | ||||||
| chr8:58647738
|
A | G | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-4665T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647738 | ||||||
| chr8:58647789
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-4716G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58647789 | ||||||
| chr8:58648391
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-5318A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648391 | ||||||
| chr8:58648574
|
C | T | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-5501G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648574 | ||||||
| chr8:58648772
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-5699C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648772 | ||||||
| chr8:58648793
|
A | G | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.60-5720T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648793 | ||||||
| chr8:58648908
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-5835T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648908 | ||||||
| chr8:58648940
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-5867A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648940 | ||||||
| chr8:58648979
|
C | T | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.60-5906G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58648979 | ||||||
| chr8:58649079
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0208 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.60-6006C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649079 | ||||||
| chr8:58649181
|
T | C | 1 | a0002c0002t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.60-6108A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649181 | ||||||
| chr8:58649186
|
G | T | 200 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(197): Show | 210 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.60-6113C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649186 | ||||||
| chr8:58649233
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-6160C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649233 | ||||||
| chr8:58649350
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.60-6277G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649350 | ||||||
| chr8:58649528
|
G | A | 200 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(197): Show | 210 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.60-6455C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649528 | ||||||
| chr8:58649546
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.60-6473C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649546 | ||||||
| chr8:58649628
|
C | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-6555G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649628 | ||||||
| chr8:58649634
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.60-6561C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649634 | ||||||
| chr8:58649700
|
A | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-6627T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649700 | ||||||
| chr8:58649926
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0208 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.60-6853A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58649926 | ||||||
| chr8:58650097
|
A | C | 218 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(215): Show | 229 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.60-7024T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650097 | ||||||
| chr8:58650256
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-7183C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650256 | ||||||
| chr8:58650442
|
ATTTTCT | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-7375_60-7370del others(6): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650442 | ||||||
| chr8:58650450
|
T | C | 1 | a0001c0001t0002g0146 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.60-7377A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650450 | ||||||
| chr8:58650866
|
T | A | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.60-7793A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650866 | ||||||
| chr8:58650934
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0208a0001c0004t0001g0116others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-7861G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58650934 | ||||||
| chr8:58651005
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.60-7932A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651005 | ||||||
| chr8:58651070
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.60-7997G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651070 | ||||||
| chr8:58651228
|
A | G | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60-8155T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651228 | ||||||
| chr8:58651336
|
G | C | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.59+8237C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651336 | ||||||
| chr8:58651438
|
A | G | 2 | a0005c0015t0009g0034a0005c0016t0006g0102 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.59+8135T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651438 | ||||||
| chr8:58651441
|
A | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 62 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.59+8132T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651441 | ||||||
| chr8:58651537
|
C | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+8036G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651537 | ||||||
| chr8:58651556
|
C | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+8017G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651556 | ||||||
| chr8:58651572
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59+8001C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651572 | ||||||
| chr8:58651573
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.59+8000T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651573 | ||||||
| chr8:58651757
|
C | A | 4 | a0001c0004t0001g0116a0003c0005t0003g0044a0005c0015t0009g0034others(1): Show | 4 | HG02572.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+7816G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651757 | ||||||
| chr8:58651763
|
G | A | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.59+7810C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651763 | ||||||
| chr8:58651797
|
G | A | 4 | a0001c0004t0001g0116a0003c0005t0003g0044a0005c0015t0009g0034others(1): Show | 4 | HG02572.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+7776C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651797 | ||||||
| chr8:58651886
|
G | A | 1 | a0001c0003t0001g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.59+7687C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58651886 | ||||||
| chr8:58652157
|
G | A | 1 | a0001c0004t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.59+7416C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652157 | ||||||
| chr8:58652244
|
A | G | 7 | a0001c0001t0001g0119a0001c0001t0001g0152a0001c0001t0001g0270others(4): Show | 7 | NA18949.hp2 NA18978.hp2 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.59+7329T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652244 | ||||||
| chr8:58652401
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59+7172G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652401 | ||||||
| chr8:58652429
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59+7144T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652429 | ||||||
| chr8:58652485
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59+7088A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652485 | ||||||
| chr8:58652514
|
G | A | 70 | a0001c0001t0001g0069a0001c0001t0001g0138a0001c0001t0001g0149others(67): Show | 73 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.59+7059C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652514 | ||||||
| chr8:58652692
|
C | A | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.59+6881G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652692 | ||||||
| chr8:58652922
|
G | A | 14 | a0001c0001t0001g0208a0001c0001t0002g0099a0001c0001t0002g0100others(11): Show | 14 | HG00408.hp1 HG02572.hp1 HG03130.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+6651C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652922 | ||||||
| chr8:58652958
|
C | T | 13 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0256others(10): Show | 13 | HG00408.hp1 HG02572.hp1 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+6615G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652958 | ||||||
| chr8:58652959
|
A | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0275 | 2 | NA19075.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.59+6614T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58652959 | ||||||
| chr8:58653084
|
G | A | 9 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0256others(6): Show | 9 | HG00408.hp1 HG02572.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+6489C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653084 | ||||||
| chr8:58653093
|
C | G | 24 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0176others(21): Show | 24 | HG00408.hp1 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+6480G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653093 | ||||||
| chr8:58653106
|
C | T | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+6467G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653106 | ||||||
| chr8:58653130
|
GAGAGT | G | 13 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0256others(10): Show | 13 | HG00408.hp1 HG02572.hp1 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+6438_59+6442del others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653130 | ||||||
| chr8:58653159
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.59+6414G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653159 | ||||||
| chr8:58653186
|
G | A | 16 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0176others(13): Show | 17 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.59+6387C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653186 | ||||||
| chr8:58653273
|
C | T | 1 | a0005c0015t0009g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59+6300G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653273 | ||||||
| chr8:58653286
|
G | T | 8 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0256others(5): Show | 8 | HG00408.hp1 NA18747.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.59+6287C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653286 | ||||||
| chr8:58653307
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.59+6266T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653307 | ||||||
| chr8:58653461
|
AC | A | 64 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0149others(61): Show | 67 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.59+6111delG | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653461 | ||||||
| chr8:58653498
|
A | T | 10 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0256others(7): Show | 10 | HG00408.hp1 HG02572.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.59+6075T>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653498 | ||||||
| chr8:58653571
|
GAAGTA | G | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5997_59+6001del others(5): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653571 | ||||||
| chr8:58653609
|
C | T | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59+5964G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653609 | ||||||
| chr8:58653635
|
T | G | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5938A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653635 | ||||||
| chr8:58653780
|
C | A | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59+5793G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653780 | ||||||
| chr8:58653799
|
T | A | 1 | a0002c0002t0002g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.59+5774A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653799 | ||||||
| chr8:58653831
|
T | A | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5742A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653831 | ||||||
| chr8:58653850
|
T | A | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.59+5723A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653850 | ||||||
| chr8:58653944
|
C | T | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5629G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653944 | ||||||
| chr8:58653956
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59+5617A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58653956 | ||||||
| chr8:58654016
|
T | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+5557A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654016 | ||||||
| chr8:58654278
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.59+5295A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654278 | ||||||
| chr8:58654321
|
G | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+5252C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654321 | ||||||
| chr8:58654340
|
C | A | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59+5233G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654340 | ||||||
| chr8:58654433
|
T | C | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+5140A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654433 | ||||||
| chr8:58654491
|
G | A | 2 | a0001c0004t0001g0116a0003c0005t0003g0044 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+5082C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654491 | ||||||
| chr8:58654555
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.59+5018T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654555 | ||||||
| chr8:58654580
|
C | T | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+4993G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654580 | ||||||
| chr8:58654609
|
T | C | 32 | a0001c0001t0001g0139a0001c0001t0001g0192a0001c0001t0001g0263others(29): Show | 34 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.59+4964A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654609 | ||||||
| chr8:58654787
|
C | A | 1 | a0003c0005t0002g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.59+4786G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654787 | ||||||
| chr8:58654830
|
C | T | 229 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0057others(226): Show | 240 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.59+4743G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654830 | ||||||
| chr8:58654959
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0139a0001c0001t0001g0169others(2): Show | 5 | HG00621.hp1 HG02135.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+4614G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58654959 | ||||||
| chr8:58655036
|
A | C | 1 | a0001c0001t0003g0047 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.59+4537T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655036 | ||||||
| chr8:58655088
|
C | A | 108 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(105): Show | 114 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.59+4485G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655088 | ||||||
| chr8:58655164
|
G | A | 2 | a0002c0002t0001g0272a0002c0002t0001g0296 | 2 | NA18949.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.59+4409C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655164 | ||||||
| chr8:58655236
|
G | T | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+4337C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655236 | ||||||
| chr8:58655252
|
G | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59+4321C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655252 | ||||||
| chr8:58655288
|
A | G | 1 | a0002c0002t0001g0272 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.59+4285T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655288 | ||||||
| chr8:58655303
|
T | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+4270A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655303 | ||||||
| chr8:58655326
|
G | T | 76 | a0001c0001t0001g0016a0001c0001t0001g0089a0001c0001t0001g0093others(73): Show | 81 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.59+4247C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655326 | ||||||
| chr8:58655329
|
G | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59+4244C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655329 | ||||||
| chr8:58655358
|
T | C | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+4215A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655358 | ||||||
| chr8:58655399
|
CT | C | 104 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0149others(101): Show | 109 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.59+4173delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655399 | ||||||
| chr8:58655477
|
G | GT | 32 | a0001c0001t0001g0139a0001c0001t0001g0192a0001c0001t0001g0263others(29): Show | 34 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.59+4095dupA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655477 | ||||||
| chr8:58655616
|
T | C | 27 | a0001c0001t0001g0192a0001c0001t0001g0263a0001c0001t0001g0340others(24): Show | 29 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.59+3957A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655616 | ||||||
| chr8:58655708
|
C | G | 1 | a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.59+3865G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655708 | ||||||
| chr8:58655732
|
T | C | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3841A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655732 | ||||||
| chr8:58655824
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.59+3749C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655824 | ||||||
| chr8:58655840
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3733C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655840 | ||||||
| chr8:58655851
|
G | T | 32 | a0001c0001t0001g0139a0001c0001t0001g0192a0001c0001t0001g0263others(29): Show | 34 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.59+3722C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655851 | ||||||
| chr8:58655852
|
G | A | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3721C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655852 | ||||||
| chr8:58655855
|
T | C | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3718A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655855 | ||||||
| chr8:58655885
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0011g0039a0005c0015t0009g0034others(2): Show | 5 | HG02970.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+3688G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655885 | ||||||
| chr8:58655895
|
A | C | 63 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0149others(60): Show | 66 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.59+3678T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655895 | ||||||
| chr8:58655907
|
T | TA | 27 | a0001c0001t0001g0192a0001c0001t0001g0263a0001c0001t0001g0340others(24): Show | 29 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.59+3665dupT | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655907 | ||||||
| chr8:58655917
|
C | A | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3656G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655917 | ||||||
| chr8:58655966
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.59+3607T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58655966 | ||||||
| chr8:58656007
|
T | C | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3566A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656007 | ||||||
| chr8:58656016
|
CT | C | 32 | a0001c0001t0001g0139a0001c0001t0001g0192a0001c0001t0001g0263others(29): Show | 34 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.59+3556delA | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656016 | ||||||
| chr8:58656023
|
TTG | T | 63 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0149others(60): Show | 66 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.59+3548_59+3549del others(2): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656023 | ||||||
| chr8:58656025
|
G | T | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3548C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656025 | ||||||
| chr8:58656029
|
G | T | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3544C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656029 | ||||||
| chr8:58656033
|
G | T | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3540C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656033 | ||||||
| chr8:58656121
|
C | G | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0175others(10): Show | 13 | HG00741.hp2 HG01069.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.59+3452G>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656121 | ||||||
| chr8:58656156
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.59+3417G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656156 | ||||||
| chr8:58656211
|
C | A | 5 | a0001c0001t0002g0191a0001c0001t0002g0329a0001c0001t0002g0330others(2): Show | 5 | NA18947.hp1 NA18964.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+3362G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656211 | ||||||
| chr8:58656282
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0101a0001c0001t0001g0115others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3291C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656282 | ||||||
| chr8:58656404
|
A | C | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3169T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656404 | ||||||
| chr8:58656488
|
G | C | 5 | a0001c0001t0001g0139a0001c0001t0011g0039a0005c0015t0009g0034others(2): Show | 5 | HG02970.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+3085C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656488 | ||||||
| chr8:58656597
|
CGGGT | C | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2972_59+2975del others(4): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656597 | ||||||
| chr8:58656612
|
C | T | 1 | a0001c0003t0003g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.59+2961G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656612 | ||||||
| chr8:58656697
|
A | G | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2876T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656697 | ||||||
| chr8:58656779
|
A | G | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2794T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656779 | ||||||
| chr8:58656788
|
C | A | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2785G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656788 | ||||||
| chr8:58656857
|
A | G | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2716T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58656857 | ||||||
| chr8:58657099
|
G | A | 2 | a0003c0005t0001g0212a0003c0005t0009g0035 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59+2474C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657099 | ||||||
| chr8:58657331
|
C | T | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2242G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657331 | ||||||
| chr8:58657341
|
C | A | 1 | a0005c0016t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.59+2232G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657341 | ||||||
| chr8:58657397
|
A | AAGTTTTC others(13): Show |
10 | a0001c0001t0001g0138a0001c0001t0008g0036a0001c0001t0008g0041others(7): Show | 10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2156_59+2175dup others(20): Show |
NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657397 | ||||||
| chr8:58657464
|
C | A | 1 | a0003c0005t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59+2109G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657464 | ||||||
| chr8:58657494
|
A | G | 10 | a0001c0001t0001g0138a0001c0001t0008g0036a0001c0001t0008g0041others(7): Show | 10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2079T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657494 | ||||||
| chr8:58657531
|
G | C | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2042C>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657531 | ||||||
| chr8:58657549
|
A | G | 1 | a0001c0001t0002g0334 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.59+2024T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657549 | ||||||
| chr8:58657569
|
A | G | 1 | a0001c0001t0014g0260 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.59+2004T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657569 | ||||||
| chr8:58657617
|
C | A | 152 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0089others(149): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.59+1956G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657617 | ||||||
| chr8:58657650
|
A | G | 4 | a0001c0004t0001g0116a0003c0005t0001g0212a0003c0005t0003g0044others(1): Show | 4 | HG03130.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+1923T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657650 | ||||||
| chr8:58657714
|
T | G | 3 | a0001c0001t0001g0136a0001c0004t0001g0116a0003c0005t0003g0044 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59+1859A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657714 | ||||||
| chr8:58657768
|
C | T | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59+1805G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657768 | ||||||
| chr8:58657828
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.59+1745T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657828 | ||||||
| chr8:58657869
|
T | C | 3 | a0002c0002t0001g0077a0002c0002t0001g0141a0002c0002t0001g0333 | 3 | HG01168.hp1 NA18954.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.59+1704A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657869 | ||||||
| chr8:58657915
|
A | G | 66 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0149others(63): Show | 69 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.59+1658T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657915 | ||||||
| chr8:58657924
|
A | G | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.59+1649T>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657924 | ||||||
| chr8:58657937
|
T | C | 6 | a0001c0001t0002g0257a0001c0001t0002g0334a0001c0001t0002g0335others(3): Show | 6 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.59+1636A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657937 | ||||||
| chr8:58657952
|
T | C | 28 | a0001c0001t0001g0136a0001c0001t0001g0166a0001c0001t0001g0192others(25): Show | 29 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.59+1621A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58657952 | ||||||
| chr8:58658060
|
C | T | 4 | a0001c0001t0001g0166a0001c0001t0001g0194a0001c0001t0001g0209others(1): Show | 4 | HG02280.hp1 HG02602.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+1513G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658060 | ||||||
| chr8:58658116
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.59+1457A>C | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658116 | ||||||
| chr8:58658208
|
T | A | 25 | a0001c0001t0001g0104a0001c0001t0001g0136a0001c0001t0001g0139others(22): Show | 26 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.59+1365A>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658208 | ||||||
| chr8:58658572
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0261a0001c0001t0002g0114 | 3 | HG01978.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.59+1001A>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658572 | ||||||
| chr8:58658624
|
G | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0115a0001c0001t0001g0138others(9): Show | 12 | HG01109.hp1 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.59+949C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658624 | ||||||
| chr8:58658632
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.59+941G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658632 | ||||||
| chr8:58658667
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.59+906G>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658667 | ||||||
| chr8:58658675
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.59+898G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658675 | ||||||
| chr8:58658728
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0054others(192): Show | 208 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.59+845G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658728 | ||||||
| chr8:58658969
|
C | T | 1 | a0001c0001t0003g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59+604G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658969 | ||||||
| chr8:58658988
|
C | T | 6 | a0001c0001t0001g0139a0001c0001t0001g0213a0001c0001t0002g0214others(3): Show | 6 | HG02615.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.59+585G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658988 | ||||||
| chr8:58658989
|
G | T | 166 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0057others(163): Show | 175 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(172): Show |
intron_variant | MODIFIER | c.59+584C>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58658989 | ||||||
| chr8:58659128
|
G | A | 1 | a0001c0001t0008g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.59+445C>T | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58659128 | ||||||
| chr8:58659236
|
C | T | 7 | a0001c0001t0002g0052a0001c0001t0006g0053a0001c0001t0008g0036others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.59+337G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58659236 | ||||||
| chr8:58659270
|
C | T | 8 | a0001c0001t0003g0007a0001c0001t0003g0040a0001c0001t0008g0036others(5): Show | 9 | HG01243.hp2 HG02486.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+303G>A | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58659270 | ||||||
| chr8:58659297
|
A | C | 145 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0057others(142): Show | 154 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.59+276T>G | NSMAF | ENSG00000035681.9 | transcript | ENST00000038176.8 | protein_coding | 1/30 | chr8 | 58659297 |