| geneid | 6491 |
|---|---|
| ensemblid | ENSG00000123473.17 |
| hgncid | 10879 |
| symbol | STIL |
| name | STIL centriolar assembly protein |
| refseq_nuc | NM_001048166.1 |
| refseq_prot | NP_001041631.1 |
| ensembl_nuc | ENST00000371877.8 |
| ensembl_prot | ENSP00000360944.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 47250139 |
| end | 47314147 |
| strand | - |
| ver | v1.2 |
| region | chr1:47250139-47314147 |
| region5000 | chr1:47245139-47319147 |
| regionname0 | STIL_chr1_47250139_47314147 |
| regionname5000 | STIL_chr1_47245139_47319147 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1288 | 193 | 59 | 22 | 99 | 3 | 10 | 79 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002 | 1/1 | 1288 | 124 | 4 | 25 | 71 | 7 | 15 | 58 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0003 | 0/0 | 1288 | 57 | 23 | 13 | 2 | 5 | 14 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0004 | 0/0 | 1288 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0005 | 0/0 | 1288 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0006 | 0/0 | 1288 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0007 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0008 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0009 | 0/0 | 1288 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0010 | 0/0 | 1288 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0011 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0012 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0013 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0014 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0015 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| 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 | 3867 | 122 | 4 | 25 | 70 | 7 | 15 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0002 | 0/0 | 3867 | 99 | 33 | 4 | 56 | 0 | 6 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0003 | 0/0 | 3867 | 94 | 26 | 18 | 43 | 3 | 4 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0004 | 0/0 | 3867 | 56 | 23 | 13 | 2 | 5 | 13 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0005 | 0/0 | 3867 | 4 | 4 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0006 | 0/0 | 3867 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0007 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0008 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0009 | 1/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0010 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0011 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0012 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0013 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0014 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0015 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0016 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0017 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0018 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0019 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| c0020 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| 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 | 1153 | 221 | 50 | 34 | 103 | 8 | 25 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0002 | 0/1 | 1151 | 123 | 7 | 25 | 68 | 7 | 15 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0003 | 0/0 | 1153 | 26 | 25 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0004 | 0/0 | 1153 | 8 | 8 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0005 | 0/0 | 1151 | 3 | 0 | 0 | 3 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0006 | 0/0 | 1153 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0007 | 0/0 | 1153 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0008 | 0/0 | 1153 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0009 | 0/0 | 1151 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0010 | 0/0 | 1153 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0011 | 0/0 | 1151 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0012 | 0/0 | 1153 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0013 | 0/0 | 1151 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0014 | 0/0 | 1153 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| t0015 | 0/0 | 1151 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 3867 | 99 | 33 | 4 | 56 | 0 | 6 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0001c0003 | 0/0 | 3867 | 94 | 26 | 18 | 43 | 3 | 4 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0001 | 0/1 | 3867 | 122 | 4 | 25 | 70 | 7 | 15 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0009 | 1/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0011 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0003c0004 | 0/0 | 3867 | 56 | 23 | 13 | 2 | 5 | 13 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0003c0015 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0004c0005 | 0/0 | 3867 | 4 | 4 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0005c0007 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0005c0017 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0006c0006 | 0/0 | 3867 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0007c0008 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0008c0012 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0009c0010 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0010c0019 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0011c0018 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0012c0013 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0013c0020 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0014c0014 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0015c0016 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 5019 | 67 | 3 | 3 | 55 | 0 | 6 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0001c0002t0003 | 0/0 | 5019 | 26 | 25 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0001c0002t0004 | 0/0 | 5019 | 5 | 5 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0001c0002t0012 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0001c0003t0001 | 0/0 | 5019 | 90 | 24 | 17 | 42 | 3 | 4 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0001c0003t0006 | 0/0 | 5019 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0001c0003t0007 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0001c0003t0010 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0001t0002 | 0/1 | 5017 | 115 | 3 | 25 | 65 | 6 | 15 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0001t0005 | 0/0 | 5017 | 3 | 0 | 0 | 3 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0001t0009 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0001t0011 | 0/0 | 5017 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0001t0013 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0001t0015 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0009t0001 | 1/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0002c0011t0002 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0003c0004t0001 | 0/0 | 5019 | 55 | 23 | 12 | 2 | 5 | 13 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0003c0004t0014 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0003c0015t0001 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0004c0005t0002 | 0/0 | 5017 | 4 | 4 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0005c0007t0004 | 0/0 | 5019 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0005c0017t0004 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0006c0006t0001 | 0/0 | 5019 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0007c0008t0002 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0008c0012t0002 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0009c0010t0002 | 0/0 | 5017 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0010c0019t0001 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0011c0018t0008 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0012c0013t0001 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0013c0020t0001 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0014c0014t0001 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| a0015c0016t0001 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | copy fasta | chr1 | 47245139 | 47319147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0002t0012g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0001c0003t0010g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0002g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0009g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0011g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0013g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0001t0015g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0009t0001g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0002c0011t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0004t0014g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0003c0015t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0004c0005t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0004c0005t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0004c0005t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0004c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0005c0007t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0005c0007t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0005c0017t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0006c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0006c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0007c0008t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0008c0012t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0009c0010t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0010c0019t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0011c0018t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0012c0013t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0013c0020t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0014c0014t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| a0015c0016t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0001 | g0340 | EUR | GBR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00099 | hp2 | a0002 | c0001 | t0002 | g0253 | EUR | GBR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00140 | hp1 | a0002 | c0001 | t0002 | g0309 | EUR | GBR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00140 | hp2 | a0002 | c0001 | t0011 | g0306 | EUR | GBR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00280 | hp1 | a0002 | c0001 | t0002 | g0263 | EUR | FIN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00280 | hp2 | a0002 | c0001 | t0002 | g0052 | EUR | FIN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00323 | hp1 | a0009 | c0010 | t0002 | g0301 | EUR | FIN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00323 | hp2 | a0003 | c0004 | t0001 | g0349 | EUR | FIN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00408 | hp1 | a0002 | c0001 | t0002 | g0285 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00597 | hp1 | a0002 | c0001 | t0002 | g0307 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00597 | hp2 | a0003 | c0004 | t0001 | g0355 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00609 | hp1 | a0002 | c0001 | t0002 | g0055 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00621 | hp2 | a0002 | c0001 | t0002 | g0252 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0185 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0219 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00642 | hp1 | a0003 | c0004 | t0001 | g0025 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00642 | hp2 | a0003 | c0004 | t0001 | g0373 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00673 | hp2 | a0002 | c0001 | t0002 | g0040 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00735 | hp1 | a0003 | c0004 | t0014 | g0370 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0346 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00738 | hp1 | a0002 | c0001 | t0002 | g0265 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00738 | hp2 | a0015 | c0016 | t0001 | g0368 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00741 | hp1 | a0002 | c0001 | t0002 | g0310 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG00741 | hp2 | a0003 | c0004 | t0001 | g0347 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01069 | hp1 | a0002 | c0001 | t0002 | g0234 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01071 | hp1 | a0002 | c0001 | t0002 | g0317 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01071 | hp2 | a0002 | c0001 | t0002 | g0233 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01074 | hp1 | a0002 | c0001 | t0002 | g0236 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0117 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01081 | hp1 | a0002 | c0001 | t0002 | g0315 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0345 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0110 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01099 | hp2 | a0002 | c0001 | t0002 | g0308 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01106 | hp1 | a0003 | c0004 | t0001 | g0348 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0080 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01167 | hp1 | a0003 | c0004 | t0001 | g0337 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01167 | hp2 | a0001 | c0003 | t0007 | g0005 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0111 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01168 | hp2 | a0002 | c0001 | t0002 | g0244 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0332 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01169 | hp2 | a0002 | c0001 | t0002 | g0286 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01175 | hp1 | a0002 | c0001 | t0002 | g0245 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0331 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01192 | hp1 | a0002 | c0001 | t0002 | g0249 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01192 | hp2 | a0003 | c0004 | t0001 | g0334 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01257 | hp1 | a0003 | c0004 | t0001 | g0341 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01257 | hp2 | a0002 | c0001 | t0002 | g0057 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01258 | hp1 | a0003 | c0004 | t0001 | g0004 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01258 | hp2 | a0002 | c0001 | t0002 | g0303 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01346 | hp1 | a0002 | c0001 | t0002 | g0260 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01358 | hp1 | a0003 | c0004 | t0001 | g0333 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0085 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01361 | hp1 | a0002 | c0001 | t0002 | g0314 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01361 | hp2 | a0002 | c0001 | t0002 | g0237 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01433 | hp1 | a0002 | c0001 | t0002 | g0270 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0127 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01496 | hp1 | a0002 | c0001 | t0002 | g0299 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0108 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0189 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01515 | hp2 | a0003 | c0004 | t0001 | g0339 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01516 | hp1 | a0003 | c0004 | t0001 | g0336 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0114 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0102 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01517 | hp2 | a0003 | c0004 | t0001 | g0335 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0231 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01884 | hp2 | a0005 | c0007 | t0004 | g0214 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0216 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0082 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01934 | hp2 | a0002 | c0001 | t0002 | g0262 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0116 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0205 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01978 | hp1 | a0002 | c0001 | t0002 | g0246 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01993 | hp1 | a0002 | c0001 | t0002 | g0254 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01993 | hp2 | a0012 | c0013 | t0001 | g0206 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02004 | hp2 | a0002 | c0001 | t0002 | g0318 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0192 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02040 | hp1 | a0002 | c0001 | t0002 | g0050 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0104 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02055 | hp1 | a0003 | c0004 | t0001 | g0365 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02056 | hp1 | a0002 | c0001 | t0002 | g0041 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02071 | hp2 | a0002 | c0001 | t0002 | g0272 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02083 | hp1 | a0002 | c0001 | t0002 | g0320 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0120 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02132 | hp2 | a0002 | c0001 | t0002 | g0385 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0229 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0325 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02148 | hp1 | a0002 | c0001 | t0002 | g0269 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0103 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02155 | hp1 | a0002 | c0001 | t0002 | g0045 | EAS | CDX | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | CDX | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02165 | hp1 | a0002 | c0001 | t0002 | g0274 | EAS | CDX | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02165 | hp2 | a0002 | c0001 | t0002 | g0047 | EAS | CDX | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0019 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0227 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02258 | hp1 | a0002 | c0001 | t0013 | g0062 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02258 | hp2 | a0002 | c0001 | t0002 | g0266 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02280 | hp1 | a0003 | c0004 | t0001 | g0031 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02523 | hp2 | a0001 | c0003 | t0010 | g0199 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0023 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0217 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02602 | hp1 | a0010 | c0019 | t0001 | g0177 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02602 | hp2 | a0002 | c0001 | t0002 | g0304 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02615 | hp1 | a0004 | c0005 | t0002 | g0065 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02615 | hp2 | a0003 | c0004 | t0001 | g0353 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02622 | hp1 | a0002 | c0001 | t0002 | g0042 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0007 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0228 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0223 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0364 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02683 | hp1 | a0002 | c0001 | t0002 | g0267 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02683 | hp2 | a0003 | c0004 | t0001 | g0344 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0128 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02698 | hp2 | a0003 | c0004 | t0001 | g0338 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0327 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02717 | hp2 | a0004 | c0005 | t0002 | g0066 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02735 | hp1 | a0003 | c0004 | t0001 | g0359 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02735 | hp2 | a0003 | c0004 | t0001 | g0369 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02738 | hp1 | a0003 | c0004 | t0001 | g0360 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02738 | hp2 | a0002 | c0001 | t0002 | g0296 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02809 | hp2 | a0003 | c0004 | t0001 | g0366 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02818 | hp1 | a0004 | c0005 | t0002 | g0064 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02818 | hp2 | a0002 | c0001 | t0002 | g0056 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0226 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0211 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0328 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02896 | hp2 | a0003 | c0004 | t0001 | g0376 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0330 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02922 | hp2 | a0003 | c0004 | t0001 | g0380 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0382 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02970 | hp1 | a0011 | c0018 | t0008 | g0212 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0351 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0324 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03017 | hp1 | a0002 | c0001 | t0002 | g0035 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03017 | hp2 | a0003 | c0004 | t0001 | g0357 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03041 | hp1 | a0003 | c0004 | t0001 | g0377 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0218 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03098 | hp1 | a0003 | c0004 | t0001 | g0352 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0022 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0021 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03139 | hp2 | a0003 | c0004 | t0001 | g0361 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0024 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03225 | hp2 | a0001 | c0003 | t0006 | g0027 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03239 | hp2 | a0002 | c0001 | t0002 | g0275 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0020 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03453 | hp2 | a0004 | c0005 | t0002 | g0063 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03486 | hp1 | a0003 | c0004 | t0001 | g0381 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0326 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0209 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03491 | hp2 | a0002 | c0001 | t0002 | g0261 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03492 | hp1 | a0002 | c0001 | t0002 | g0302 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0204 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0224 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03540 | hp1 | a0003 | c0004 | t0001 | g0363 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0378 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0222 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03654 | hp1 | a0003 | c0004 | t0001 | g0342 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0178 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0134 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03704 | hp1 | a0002 | c0001 | t0002 | g0034 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03710 | hp1 | a0002 | c0001 | t0002 | g0280 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03710 | hp2 | a0003 | c0004 | t0001 | g0372 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03831 | hp1 | a0002 | c0001 | t0002 | g0257 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03834 | hp1 | a0002 | c0001 | t0002 | g0235 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03834 | hp2 | a0003 | c0004 | t0001 | g0004 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03927 | hp1 | a0002 | c0001 | t0002 | g0240 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03927 | hp2 | a0003 | c0004 | t0001 | g0343 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03942 | hp1 | a0002 | c0001 | t0002 | g0238 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03942 | hp2 | a0003 | c0004 | t0001 | g0371 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG04184 | hp2 | a0003 | c0004 | t0001 | g0374 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG04199 | hp1 | a0003 | c0004 | t0001 | g0358 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG04199 | hp2 | a0002 | c0001 | t0002 | g0268 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG04204 | hp1 | a0003 | c0015 | t0001 | g0367 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG04204 | hp2 | a0002 | c0001 | t0002 | g0264 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0018 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18612 | hp1 | a0003 | c0004 | t0001 | g0356 | EAS | CHB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | CHB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | CHB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18747 | hp2 | a0008 | c0012 | t0002 | g0297 | EAS | CHB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0126 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18906 | hp2 | a0003 | c0004 | t0001 | g0375 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18939 | hp2 | a0002 | c0001 | t0002 | g0312 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18940 | hp2 | a0002 | c0001 | t0002 | g0032 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18942 | hp1 | a0002 | c0001 | t0002 | g0279 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18944 | hp2 | a0002 | c0001 | t0002 | g0054 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18945 | hp1 | a0002 | c0001 | t0015 | g0388 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18945 | hp2 | a0002 | c0001 | t0002 | g0383 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18946 | hp1 | a0002 | c0001 | t0002 | g0321 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18946 | hp2 | a0002 | c0001 | t0002 | g0044 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18947 | hp1 | a0002 | c0001 | t0002 | g0033 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18948 | hp2 | a0002 | c0001 | t0005 | g0242 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18949 | hp2 | a0002 | c0001 | t0002 | g0258 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18956 | hp1 | a0006 | c0006 | t0001 | g0087 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18956 | hp2 | a0002 | c0001 | t0002 | g0037 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0124 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18959 | hp2 | a0006 | c0006 | t0001 | g0141 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18961 | hp2 | a0002 | c0001 | t0002 | g0278 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18964 | hp1 | a0002 | c0001 | t0002 | g0059 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18965 | hp1 | a0013 | c0020 | t0001 | g0151 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18965 | hp2 | a0002 | c0001 | t0002 | g0061 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18966 | hp1 | a0002 | c0001 | t0002 | g0276 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18967 | hp2 | a0002 | c0001 | t0002 | g0319 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18968 | hp2 | a0002 | c0001 | t0002 | g0060 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18969 | hp2 | a0002 | c0001 | t0002 | g0290 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18970 | hp2 | a0002 | c0001 | t0002 | g0243 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18977 | hp1 | a0002 | c0001 | t0002 | g0387 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18979 | hp2 | a0002 | c0001 | t0002 | g0247 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18980 | hp2 | a0002 | c0001 | t0002 | g0287 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18982 | hp1 | a0002 | c0001 | t0002 | g0291 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18985 | hp1 | a0002 | c0001 | t0009 | g0283 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18988 | hp1 | a0002 | c0001 | t0002 | g0281 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18989 | hp1 | a0002 | c0001 | t0002 | g0305 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18991 | hp2 | a0002 | c0001 | t0002 | g0241 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18992 | hp1 | a0002 | c0001 | t0002 | g0051 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18994 | hp1 | a0002 | c0001 | t0002 | g0298 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18995 | hp1 | a0002 | c0001 | t0002 | g0300 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18998 | hp1 | a0002 | c0001 | t0002 | g0282 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18999 | hp1 | a0002 | c0001 | t0002 | g0294 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19003 | hp2 | a0002 | c0001 | t0002 | g0039 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19004 | hp1 | a0002 | c0001 | t0002 | g0036 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19004 | hp2 | a0001 | c0002 | t0012 | g0155 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19005 | hp1 | a0002 | c0001 | t0002 | g0271 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19007 | hp1 | a0002 | c0001 | t0002 | g0046 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19009 | hp1 | a0002 | c0001 | t0002 | g0292 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19012 | hp2 | a0002 | c0001 | t0002 | g0311 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19030 | hp1 | a0003 | c0004 | t0001 | g0350 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0030 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19043 | hp2 | a0005 | c0007 | t0004 | g0213 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19055 | hp1 | a0002 | c0001 | t0002 | g0386 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19055 | hp2 | a0002 | c0001 | t0002 | g0295 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19058 | hp1 | a0002 | c0001 | t0002 | g0053 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19058 | hp2 | a0002 | c0001 | t0005 | g0273 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19062 | hp1 | a0002 | c0001 | t0002 | g0255 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19063 | hp2 | a0007 | c0008 | t0002 | g0251 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19064 | hp2 | a0002 | c0001 | t0002 | g0239 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19065 | hp1 | a0002 | c0011 | t0002 | g0289 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19066 | hp2 | a0002 | c0001 | t0002 | g0284 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19072 | hp2 | a0002 | c0001 | t0002 | g0313 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19074 | hp1 | a0002 | c0001 | t0002 | g0384 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19077 | hp1 | a0002 | c0001 | t0002 | g0248 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19078 | hp2 | a0002 | c0001 | t0002 | g0043 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19080 | hp1 | a0002 | c0001 | t0002 | g0058 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19080 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19082 | hp1 | a0002 | c0001 | t0002 | g0232 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19082 | hp2 | a0014 | c0014 | t0001 | g0191 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19084 | hp1 | a0002 | c0001 | t0002 | g0048 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19085 | hp2 | a0002 | c0001 | t0002 | g0277 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19088 | hp1 | a0002 | c0001 | t0005 | g0293 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19240 | hp1 | a0003 | c0004 | t0001 | g0362 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0230 | AFR | ASW | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | ASW | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA20805 | hp1 | a0002 | c0001 | t0002 | g0259 | EUR | TSI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA20805 | hp2 | a0002 | c0001 | t0002 | g0316 | EUR | TSI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01123 | hp1 | a0002 | c0001 | t0002 | g0288 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0074 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0184 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0354 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0329 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02486 | hp2 | a0001 | c0003 | t0006 | g0026 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0097 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0221 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0136 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | USA | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| HG06807 | hp2 | a0005 | c0017 | t0004 | g0215 | AFR | USA | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18955 | hp1 | a0002 | c0001 | t0002 | g0049 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA18955 | hp2 | a0002 | c0001 | t0002 | g0256 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA20300 | hp1 | a0003 | c0004 | t0001 | g0379 | AFR | USA | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | USA | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0322 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0002 | g0250 | REF | REF | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| homoSapiens_grch38 | hp1 | a0002 | c0009 | t0001 | g0038 | REF | REF | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47251308
|
C | T | 1 | a0011 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.3695G>A | p.Arg1232Gln | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3850/5019 | 3695/3867 | 1232/1288 | chr1 | 47251308 | ||
| chr1:47251488
|
G | A | 1 | a0010 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.3515C>T | p.Ser1172Phe | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3670/5019 | 3515/3867 | 1172/1288 | chr1 | 47251488 | ||
| chr1:47251566
|
G | A | 1 | a0006 | 2 | NA18956.hp1 NA18959.hp2 |
missense_variant | MODERATE | c.3437C>T | p.Ala1146Val | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3592/5019 | 3437/3867 | 1146/1288 | chr1 | 47251566 | ||
| chr1:47251573
|
C | T | 1 | a0005 | 3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.3430G>A | p.Asp1144Asn | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3585/5019 | 3430/3867 | 1144/1288 | chr1 | 47251573 | ||
| chr1:47251708
|
T | C | 1 | a0012 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.3295A>G | p.Ile1099Val | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3450/5019 | 3295/3867 | 1099/1288 | chr1 | 47251708 | ||
| chr1:47251746
|
G | A | 1 | a0009 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.3257C>T | p.Ser1086Leu | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3412/5019 | 3257/3867 | 1086/1288 | chr1 | 47251746 | ||
| chr1:47251833
|
T | C | 1 | a0013 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.3170A>G | p.Asn1057Ser | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3325/5019 | 3170/3867 | 1057/1288 | chr1 | 47251833 | ||
| chr1:47260308
|
G | A | 1 | a0014 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.3061C>T | p.His1021Tyr | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/17 | 3216/5019 | 3061/3867 | 1021/1288 | chr1 | 47260308 | ||
| chr1:47260415
|
T | C | 2 | a0003a0015 | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
missense_variant | MODERATE | c.2954A>G | p.His985Arg | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/17 | 3109/5019 | 2954/3867 | 985/1288 | chr1 | 47260415 | ||
| chr1:47260463
|
T | C | 1 | a0015 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2906A>G | p.His969Arg | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/17 | 3061/5019 | 2906/3867 | 969/1288 | chr1 | 47260463 | ||
| chr1:47280441
|
T | C | 1 | a0004 | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.2017A>G | p.Ser673Gly | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/17 | 2172/5019 | 2017/3867 | 673/1288 | chr1 | 47280441 | ||
| chr1:47289458
|
T | C | 1 | a0008 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1000A>G | p.Lys334Glu | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/17 | 1155/5019 | 1000/3867 | 334/1288 | chr1 | 47289458 | ||
| chr1:47301737
|
C | T | 1 | a0007 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.277G>A | p.Val93Ile | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/17 | 432/5019 | 277/3867 | 93/1288 | chr1 | 47301737 | ||
| chr1:47302242
|
G | A | 10 | a0001a0003a0005others(7): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
missense_variant | MODERATE | c.257C>T | p.Ala86Val | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 4/17 | 412/5019 | 257/3867 | 86/1288 | chr1 | 47302242 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47251217
|
C | T | 2 | a0003c0015a0015c0016 | 2 | HG00738.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.3786G>A | p.Thr1262Thr | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3941/5019 | 3786/3867 | 1262/1288 | chr1 | 47251217 | ||
| chr1:47251517
|
A | G | 7 | a0002c0001a0002c0011a0004c0005others(4): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
synonymous_variant | LOW | c.3486T>C | p.Pro1162Pro | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3641/5019 | 3486/3867 | 1162/1288 | chr1 | 47251517 | ||
| chr1:47281006
|
G | C | 6 | a0001c0002a0005c0007a0005c0017others(3): Show | 105 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(102): Show |
synonymous_variant | LOW | c.1452C>G | p.Ser484Ser | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/17 | 1607/5019 | 1452/3867 | 484/1288 | chr1 | 47281006 | ||
| chr1:47282414
|
G | A | 1 | a0002c0011 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.1179C>T | p.His393His | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/17 | 1334/5019 | 1179/3867 | 393/1288 | chr1 | 47282414 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47250144
|
T | C | 1 | a0002c0001t0009 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 992 | chr1 | 47250144 | |||||
| chr1:47250226
|
A | G | 1 | a0011c0018t0008 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*910T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 910 | chr1 | 47250226 | |||||
| chr1:47250253
|
T | C | 1 | a0002c0001t0005 | 3 | NA18948.hp2 NA19058.hp2 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*883A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 883 | chr1 | 47250253 | |||||
| chr1:47250368
|
TAA | T | 11 | a0002c0001t0002a0002c0001t0005a0002c0001t0009others(8): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*766_*767delTT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 766 | chr1 | 47250368 | |||||
| chr1:47250406
|
T | C | 1 | a0001c0003t0010 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*730A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 730 | chr1 | 47250406 | |||||
| chr1:47250559
|
C | T | 1 | a0001c0002t0003 | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*577G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 577 | chr1 | 47250559 | |||||
| chr1:47250591
|
G | A | 1 | a0002c0001t0011 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*545C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 545 | chr1 | 47250591 | |||||
| chr1:47250605
|
A | C | 1 | a0001c0003t0006 | 2 | HG02486.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*531T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 531 | chr1 | 47250605 | |||||
| chr1:47250609
|
C | A | 1 | a0001c0002t0012 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 527 | chr1 | 47250609 | |||||
| chr1:47250820
|
A | G | 5 | a0001c0002t0003a0001c0002t0004a0005c0007t0004others(2): Show | 35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*316T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 316 | chr1 | 47250820 | |||||
| chr1:47250868
|
G | C | 1 | a0002c0001t0013 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*268C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 268 | chr1 | 47250868 | |||||
| chr1:47251013
|
T | C | 1 | a0003c0004t0014 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*123A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 123 | chr1 | 47251013 | |||||
| chr1:47314094
|
G | C | 1 | a0002c0001t0015 | 1 | NA18945.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-102C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/17 | chr1 | 47314094 | ||||||
| chr1:47314113
|
G | T | 1 | a0001c0003t0007 | 1 | HG01167.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/17 | 3794 | chr1 | 47314113 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47252110
|
G | C | 1 | a0001c0003t0001g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3081-188C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252110 | ||||||
| chr1:47252137
|
T | C | 1 | a0003c0004t0001g0364 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3081-215A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252137 | ||||||
| chr1:47252202
|
A | G | 1 | a0001c0002t0001g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3081-280T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252202 | ||||||
| chr1:47252333
|
G | A | 2 | a0003c0004t0001g0365a0003c0004t0001g0366 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3081-411C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252333 | ||||||
| chr1:47252337
|
G | A | 1 | a0002c0001t0002g0032 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3081-415C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252337 | ||||||
| chr1:47252346
|
C | T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3081-424G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252346 | ||||||
| chr1:47252363
|
C | T | 9 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3081-441G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252363 | ||||||
| chr1:47252433
|
C | T | 1 | a0003c0004t0001g0346 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3081-511G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252433 | ||||||
| chr1:47252463
|
A | G | 1 | a0001c0002t0003g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3081-541T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252463 | ||||||
| chr1:47252646
|
A | G | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3081-724T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252646 | ||||||
| chr1:47252686
|
G | A | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3081-764C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252686 | ||||||
| chr1:47252778
|
T | TAC | 45 | a0001c0002t0001g0076a0001c0002t0001g0077a0001c0002t0001g0078others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.3081-858_3081-857d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
T | TACAC | 33 | a0001c0002t0001g0172a0001c0002t0003g0227a0001c0003t0001g0074others(30): Show | 33 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3081-860_3081-857d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
T | TACACAC | 10 | a0002c0001t0002g0041a0002c0001t0002g0383a0003c0004t0001g0335others(7): Show | 10 | HG01516.hp1 HG01517.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.3081-862_3081-857d others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
T | TACACACA others(1): Show |
6 | a0003c0004t0001g0333a0003c0004t0001g0364a0003c0004t0001g0371others(3): Show | 6 | HG00738.hp2 HG01358.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3081-864_3081-857d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TAC | T | 132 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(129): Show | 133 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.3081-858_3081-857d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACAC | T | 24 | a0001c0002t0003g0007a0001c0002t0003g0009a0001c0002t0003g0012others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.3081-860_3081-857d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACACAC | T | 29 | a0001c0002t0001g0149a0001c0002t0001g0150a0001c0002t0001g0208others(26): Show | 31 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.3081-862_3081-857d others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACACACA others(1): Show |
T | 12 | a0001c0002t0003g0010a0001c0002t0003g0011a0001c0003t0001g0193others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.3081-864_3081-857d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACACACA others(5): Show |
T | 3 | a0005c0007t0004g0213a0005c0007t0004g0214a0005c0017t0004g0215 | 3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3081-868_3081-857d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACACACA others(6): Show |
T | 1 | a0001c0003t0001g0205 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3081-869_3081-857d others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACACACA others(7): Show |
T | 6 | a0001c0002t0004g0211a0001c0002t0004g0231a0001c0003t0001g0135others(3): Show | 6 | HG01884.hp1 HG01993.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3081-870_3081-857d others(16): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACACACA others(9): Show |
T | 3 | a0001c0002t0004g0228a0001c0002t0004g0229a0001c0002t0004g0230 | 3 | HG02145.hp1 HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3081-872_3081-857d others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACACACA others(17): Show |
T | 2 | a0003c0004t0001g0365a0003c0004t0001g0366 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3081-880_3081-857d others(26): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252778
|
TACACACA others(19): Show |
T | 1 | a0002c0001t0002g0285 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3081-882_3081-857d others(28): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | ||||||
| chr1:47252823
|
ACG | A | 8 | a0002c0001t0002g0040a0002c0001t0002g0043a0002c0001t0002g0046others(5): Show | 8 | HG00609.hp1 HG00673.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.3081-903_3081-902d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252823 | ||||||
| chr1:47252825
|
G | A | 3 | a0002c0001t0002g0033a0002c0001t0002g0044a0002c0001t0002g0048 | 3 | NA18946.hp2 NA18947.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3081-903C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252825 | ||||||
| chr1:47252938
|
T | C | 3 | a0005c0007t0004g0213a0005c0007t0004g0214a0005c0017t0004g0215 | 3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3081-1016A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252938 | ||||||
| chr1:47253141
|
T | C | 1 | a0009c0010t0002g0301 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3081-1219A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253141 | ||||||
| chr1:47253339
|
C | A | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3081-1417G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253339 | ||||||
| chr1:47253436
|
C | T | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3081-1514G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253436 | ||||||
| chr1:47253445
|
G | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3081-1523C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253445 | ||||||
| chr1:47253684
|
T | C | 1 | a0002c0001t0002g0278 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3081-1762A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253684 | ||||||
| chr1:47253857
|
G | A | 2 | a0001c0003t0001g0122a0001c0003t0001g0192 | 2 | HG02027.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3081-1935C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253857 | ||||||
| chr1:47254049
|
C | T | 2 | a0002c0001t0002g0250a0002c0001t0002g0318 | 2 | HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3081-2127G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254049 | ||||||
| chr1:47254050
|
G | A | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3081-2128C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254050 | ||||||
| chr1:47254150
|
C | T | 26 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(23): Show | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.3081-2228G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254150 | ||||||
| chr1:47254180
|
C | CA | 53 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0072others(50): Show | 54 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.3081-2259dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
C | CAA | 47 | a0001c0002t0001g0069a0001c0002t0001g0071a0001c0002t0001g0073others(44): Show | 48 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.3081-2260_3081-225 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
C | CAAA | 19 | a0001c0002t0001g0095a0003c0004t0001g0022a0003c0004t0001g0023others(16): Show | 19 | HG01167.hp1 HG02055.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.3081-2261_3081-225 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
CA | C | 6 | a0001c0002t0001g0169a0001c0002t0001g0179a0001c0002t0001g0187others(3): Show | 6 | HG03704.hp2 NA18951.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.3081-2259delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
CAA | C | 8 | a0002c0001t0002g0041a0002c0001t0002g0045a0002c0001t0002g0051others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3081-2260_3081-225 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
CAAA | C | 51 | a0001c0002t0003g0028a0001c0002t0003g0227a0001c0002t0003g0325others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.3081-2261_3081-225 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
CAAAA | C | 96 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.3081-2262_3081-225 others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
CAAAAA | C | 11 | a0001c0002t0003g0328a0001c0002t0004g0228a0001c0003t0001g0142others(8): Show | 11 | HG00738.hp1 HG01433.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3081-2263_3081-225 others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0001g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3081-2268_3081-225 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254180
|
CAAAAAAA others(4): Show |
C | 15 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(12): Show | 16 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3081-2269_3081-225 others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | ||||||
| chr1:47254529
|
G | GT | 26 | a0001c0002t0001g0166a0001c0002t0003g0006a0001c0002t0003g0007others(23): Show | 26 | HG00741.hp1 HG01069.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.3081-2608dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254529 | ||||||
| chr1:47254529
|
GT | G | 57 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3081-2608delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254529 | ||||||
| chr1:47254540
|
G | GT | 5 | a0002c0001t0002g0258a0004c0005t0002g0063a0004c0005t0002g0064others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3081-2619dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254540 | ||||||
| chr1:47254734
|
T | C | 2 | a0003c0004t0001g0335a0003c0004t0001g0336 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3081-2812A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254734 | ||||||
| chr1:47254962
|
G | C | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.3081-3040C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254962 | ||||||
| chr1:47254970
|
G | C | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3081-3048C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254970 | ||||||
| chr1:47255120
|
C | T | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3081-3198G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255120 | ||||||
| chr1:47255186
|
G | A | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3081-3264C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255186 | ||||||
| chr1:47255283
|
G | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3081-3361C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255283 | ||||||
| chr1:47255310
|
G | T | 26 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(23): Show | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.3081-3388C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255310 | ||||||
| chr1:47255315
|
A | T | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3081-3393T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255315 | ||||||
| chr1:47255464
|
C | T | 131 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.3081-3542G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255464 | ||||||
| chr1:47255506
|
G | A | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3081-3584C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255506 | ||||||
| chr1:47255532
|
G | A | 1 | a0001c0003t0001g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3081-3610C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255532 | ||||||
| chr1:47255550
|
C | CA | 70 | a0001c0002t0003g0011a0001c0002t0003g0021a0001c0002t0003g0028others(67): Show | 71 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.3081-3629dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255550 | ||||||
| chr1:47255550
|
C | CAA | 116 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0035others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.3081-3630_3081-362 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255550 | ||||||
| chr1:47255550
|
C | CAAA | 7 | a0002c0001t0002g0040a0002c0001t0002g0238a0002c0001t0002g0239others(4): Show | 7 | HG00673.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.3081-3631_3081-362 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255550 | ||||||
| chr1:47255550
|
CA | C | 143 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(140): Show | 145 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.3081-3629delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255550 | ||||||
| chr1:47255582
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3081-3660G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255582 | ||||||
| chr1:47255652
|
T | C | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3081-3730A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255652 | ||||||
| chr1:47255823
|
C | A | 1 | a0002c0001t0002g0309 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3081-3901G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255823 | ||||||
| chr1:47255839
|
C | T | 1 | a0001c0003t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3081-3917G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255839 | ||||||
| chr1:47256184
|
T | C | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3080+4105A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256184 | ||||||
| chr1:47256369
|
T | A | 1 | a0001c0002t0001g0072 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3080+3920A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256369 | ||||||
| chr1:47256397
|
C | G | 1 | a0004c0005t0002g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3080+3892G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256397 | ||||||
| chr1:47256584
|
A | G | 240 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.3080+3705T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256584 | ||||||
| chr1:47256620
|
C | CA | 21 | a0001c0002t0001g0181a0001c0003t0001g0003a0001c0003t0001g0098others(18): Show | 22 | HG00639.hp2 HG01167.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3080+3668dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256620 | ||||||
| chr1:47256620
|
C | CAA | 53 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(50): Show | 54 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.3080+3667_3080+366 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256620 | ||||||
| chr1:47256620
|
CA | C | 9 | a0001c0002t0001g0160a0001c0002t0003g0007a0001c0002t0003g0008others(6): Show | 9 | HG01074.hp1 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.3080+3668delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256620 | ||||||
| chr1:47256639
|
AT | A | 7 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3080+3649delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256639 | ||||||
| chr1:47256640
|
T | A | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+3649A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256640 | ||||||
| chr1:47256704
|
C | G | 1 | a0002c0001t0002g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3080+3585G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256704 | ||||||
| chr1:47256723
|
G | A | 1 | a0003c0004t0001g0022 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3080+3566C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256723 | ||||||
| chr1:47257390
|
A | C | 1 | a0001c0002t0001g0150 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3080+2899T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257390 | ||||||
| chr1:47257615
|
G | A | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+2674C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257615 | ||||||
| chr1:47257671
|
T | C | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3080+2618A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257671 | ||||||
| chr1:47257773
|
A | T | 1 | a0001c0002t0001g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3080+2516T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257773 | ||||||
| chr1:47257874
|
T | C | 1 | a0002c0001t0002g0239 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3080+2415A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257874 | ||||||
| chr1:47257902
|
T | C | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+2387A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257902 | ||||||
| chr1:47258152
|
C | G | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3080+2137G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258152 | ||||||
| chr1:47258432
|
C | T | 1 | a0001c0002t0003g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3080+1857G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258432 | ||||||
| chr1:47258494
|
C | T | 26 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(23): Show | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.3080+1795G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258494 | ||||||
| chr1:47258507
|
A | T | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3080+1782T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258507 | ||||||
| chr1:47258604
|
C | T | 69 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(66): Show | 70 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.3080+1685G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258604 | ||||||
| chr1:47258635
|
A | G | 3 | a0001c0003t0001g0086a0001c0003t0001g0133a0001c0003t0001g0143 | 3 | NA18939.hp1 NA18961.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.3080+1654T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258635 | ||||||
| chr1:47258644
|
A | C | 4 | a0003c0004t0001g0375a0003c0004t0001g0376a0003c0004t0001g0377others(1): Show | 4 | HG02896.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+1645T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258644 | ||||||
| chr1:47258728
|
T | C | 240 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.3080+1561A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258728 | ||||||
| chr1:47258861
|
C | T | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3080+1428G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258861 | ||||||
| chr1:47258928
|
TATACTTG others(3): Show |
T | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3080+1351_3080+136 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258928 | ||||||
| chr1:47258992
|
C | CTTTTTTT others(3): Show |
12 | a0001c0002t0004g0231a0001c0003t0001g0003a0001c0003t0001g0217others(9): Show | 13 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.3080+1287_3080+129 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | ||||||
| chr1:47258992
|
C | CTTTTTTT others(4): Show |
11 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0003t0001g0322others(8): Show | 11 | HG01167.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3080+1286_3080+129 others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | ||||||
| chr1:47258992
|
C | CTTTTTTT others(5): Show |
117 | a0001c0002t0003g0327a0001c0002t0003g0328a0001c0002t0003g0329others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.3080+1285_3080+129 others(16): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | ||||||
| chr1:47258992
|
C | CTTTTTTT others(6): Show |
66 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0004g0228others(63): Show | 66 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.3080+1284_3080+129 others(17): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | ||||||
| chr1:47258992
|
C | CTTTTTTT others(7): Show |
11 | a0001c0002t0003g0010a0001c0002t0003g0011a0002c0001t0002g0036others(8): Show | 11 | HG02056.hp1 HG02615.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.3080+1283_3080+129 others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | ||||||
| chr1:47258992
|
C | CTTTTTTT others(8): Show |
2 | a0002c0001t0002g0048a0002c0001t0002g0387 | 2 | NA18977.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3080+1296_3080+129 others(19): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | ||||||
| chr1:47258992
|
C | CTTTTTTT others(9): Show |
8 | a0001c0002t0003g0007a0001c0002t0003g0009a0001c0002t0003g0013others(5): Show | 8 | HG01069.hp2 HG02622.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.3080+1296_3080+129 others(20): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | ||||||
| chr1:47258992
|
C | CTTTTTTT others(10): Show |
6 | a0001c0002t0003g0006a0001c0002t0003g0008a0001c0002t0003g0012others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3080+1296_3080+129 others(21): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | ||||||
| chr1:47259011
|
C | CAG | 224 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.3080+1276_3080+127 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259011 | ||||||
| chr1:47259040
|
G | A | 1 | a0001c0003t0001g0186 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3080+1249C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259040 | ||||||
| chr1:47259087
|
C | T | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3080+1202G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259087 | ||||||
| chr1:47259096
|
C | T | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3080+1193G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259096 | ||||||
| chr1:47259193
|
A | G | 94 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(91): Show | 95 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.3080+1096T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259193 | ||||||
| chr1:47259196
|
C | T | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3080+1093G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259196 | ||||||
| chr1:47259259
|
T | TACAGGTG others(2): Show |
6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3080+1021_3080+102 others(13): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259259 | ||||||
| chr1:47259281
|
C | T | 6 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(3): Show | 6 | HG02622.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3080+1008G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259281 | ||||||
| chr1:47259285
|
C | CT | 88 | a0001c0002t0001g0145a0001c0002t0001g0150a0001c0002t0001g0168others(85): Show | 89 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.3080+1003dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | ||||||
| chr1:47259285
|
C | CTT | 40 | a0001c0002t0003g0028a0001c0002t0003g0227a0001c0002t0004g0228others(37): Show | 40 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.3080+1002_3080+100 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | ||||||
| chr1:47259285
|
C | CTTT | 85 | a0001c0002t0004g0211a0002c0001t0002g0039a0002c0001t0002g0041others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.3080+1001_3080+100 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | ||||||
| chr1:47259285
|
C | CTTTT | 15 | a0001c0002t0003g0008a0001c0002t0004g0229a0001c0002t0004g0230others(12): Show | 15 | HG00597.hp1 HG00621.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.3080+1000_3080+100 others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | ||||||
| chr1:47259285
|
CT | C | 6 | a0001c0002t0001g0069a0001c0002t0001g0073a0001c0002t0001g0156others(3): Show | 6 | HG01517.hp1 HG03688.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.3080+1003delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | ||||||
| chr1:47259285
|
CTTTTTTT others(3): Show |
C | 2 | a0002c0001t0002g0315a0002c0001t0002g0316 | 2 | HG01081.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3080+994_3080+1003 others(13): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | ||||||
| chr1:47259445
|
C | T | 2 | a0001c0002t0001g0167a0001c0002t0001g0169 | 2 | NA18951.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3080+844G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259445 | ||||||
| chr1:47259479
|
C | T | 69 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(66): Show | 70 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.3080+810G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259479 | ||||||
| chr1:47259556
|
T | C | 1 | a0001c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3080+733A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259556 | ||||||
| chr1:47259584
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3080+705G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259584 | ||||||
| chr1:47259585
|
G | A | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+704C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259585 | ||||||
| chr1:47259705
|
A | G | 3 | a0001c0003t0001g0205a0001c0003t0001g0207a0012c0013t0001g0206 | 3 | HG01975.hp2 HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3080+584T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259705 | ||||||
| chr1:47260099
|
T | A | 1 | a0001c0003t0001g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3080+190A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260099 | ||||||
| chr1:47260131
|
C | T | 1 | a0003c0004t0001g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3080+158G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260131 | ||||||
| chr1:47260145
|
A | G | 2 | a0001c0002t0004g0211a0011c0018t0008g0212 | 2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3080+144T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260145 | ||||||
| chr1:47260159
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3080+130C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260159 | ||||||
| chr1:47260206
|
C | G | 2 | a0002c0001t0002g0239a0002c0001t0002g0258 | 2 | NA18949.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3080+83G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260206 | ||||||
| chr1:47260593
|
C | T | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2830-54G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260593 | ||||||
| chr1:47260635
|
A | C | 11 | a0001c0003t0001g0003a0001c0003t0001g0217a0001c0003t0001g0218others(8): Show | 12 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2830-96T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260635 | ||||||
| chr1:47260749
|
G | C | 1 | a0001c0003t0001g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2830-210C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260749 | ||||||
| chr1:47260794
|
C | T | 2 | a0001c0002t0001g0148a0001c0002t0001g0180 | 2 | NA19009.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2830-255G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260794 | ||||||
| chr1:47260878
|
T | A | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2830-339A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260878 | ||||||
| chr1:47260963
|
A | G | 1 | a0013c0020t0001g0151 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2830-424T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260963 | ||||||
| chr1:47260996
|
T | A | 1 | a0001c0002t0012g0155 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2830-457A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260996 | ||||||
| chr1:47261133
|
A | G | 1 | a0002c0001t0002g0265 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2830-594T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261133 | ||||||
| chr1:47261245
|
G | A | 1 | a0002c0001t0002g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2830-706C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261245 | ||||||
| chr1:47261258
|
C | G | 2 | a0001c0003t0001g0102a0001c0003t0001g0189 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2830-719G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261258 | ||||||
| chr1:47261261
|
A | G | 8 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2830-722T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261261 | ||||||
| chr1:47261272
|
C | T | 1 | a0001c0003t0001g0192 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2830-733G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261272 | ||||||
| chr1:47261343
|
G | C | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2830-804C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261343 | ||||||
| chr1:47261344
|
C | T | 5 | a0001c0002t0004g0211a0001c0002t0004g0229a0001c0002t0004g0230others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2830-805G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261344 | ||||||
| chr1:47261466
|
C | T | 1 | a0001c0002t0001g0072 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2830-927G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261466 | ||||||
| chr1:47261604
|
G | A | 8 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2830-1065C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261604 | ||||||
| chr1:47261745
|
C | CA | 27 | a0001c0002t0001g0148a0001c0002t0001g0149a0001c0002t0001g0168others(24): Show | 28 | HG00639.hp2 HG01934.hp2 HG02572.hp2 others(25): Show |
intron_variant | MODIFIER | c.2829+1157dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261745 | ||||||
| chr1:47261745
|
CA | C | 94 | a0001c0002t0001g0067a0001c0002t0003g0006a0001c0002t0003g0007others(91): Show | 95 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.2829+1157delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261745 | ||||||
| chr1:47261763
|
T | A | 129 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.2829+1140A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261763 | ||||||
| chr1:47261882
|
A | C | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2829+1021T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261882 | ||||||
| chr1:47261907
|
C | CA | 15 | a0001c0002t0001g0145a0001c0002t0001g0170a0001c0002t0004g0229others(12): Show | 15 | HG01258.hp2 HG01884.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.2829+995dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261907 | ||||||
| chr1:47261907
|
CA | C | 6 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0169others(3): Show | 6 | NA18941.hp1 NA18951.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.2829+995delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261907 | ||||||
| chr1:47261962
|
T | C | 1 | a0001c0003t0006g0026 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2829+941A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261962 | ||||||
| chr1:47262232
|
G | A | 2 | a0002c0001t0002g0041a0002c0001t0002g0050 | 2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2829+671C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262232 | ||||||
| chr1:47262251
|
G | A | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2829+652C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262251 | ||||||
| chr1:47262275
|
C | G | 56 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(53): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2829+628G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262275 | ||||||
| chr1:47262385
|
A | T | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2829+518T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262385 | ||||||
| chr1:47262426
|
C | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2829+477G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262426 | ||||||
| chr1:47262481
|
T | G | 1 | a0001c0003t0001g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2829+422A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262481 | ||||||
| chr1:47262488
|
T | G | 3 | a0001c0003t0001g0097a0001c0003t0001g0125a0001c0003t0001g0126 | 3 | HG01891.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2829+415A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262488 | ||||||
| chr1:47262506
|
C | T | 1 | a0001c0002t0001g0153 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2829+397G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262506 | ||||||
| chr1:47262553
|
C | A | 13 | a0001c0003t0001g0001a0001c0003t0001g0079a0001c0003t0001g0100others(10): Show | 14 | HG00621.hp1 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2829+350G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262553 | ||||||
| chr1:47262766
|
A | G | 1 | a0002c0001t0002g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2829+137T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262766 | ||||||
| chr1:47262787
|
A | G | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2829+116T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262787 | ||||||
| chr1:47262818
|
C | T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2829+85G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262818 | ||||||
| chr1:47263354
|
G | T | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-238C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263354 | ||||||
| chr1:47263362
|
T | A | 32 | a0002c0001t0002g0033a0002c0001t0002g0034a0002c0001t0002g0035others(29): Show | 32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2616-246A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263362 | ||||||
| chr1:47263362
|
T | G | 208 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2616-246A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263362 | ||||||
| chr1:47263626
|
A | G | 1 | a0002c0001t0002g0265 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2616-510T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263626 | ||||||
| chr1:47263744
|
G | GT | 43 | a0001c0002t0001g0070a0001c0002t0001g0073a0001c0002t0001g0091others(40): Show | 44 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2616-629dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
G | GTT | 10 | a0001c0002t0003g0227a0001c0002t0003g0327a0001c0002t0003g0330others(7): Show | 10 | HG01978.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2616-630_2616-629d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
G | GTTT | 7 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0328others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2616-631_2616-629d others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
G | GTTTTT | 9 | a0003c0004t0001g0023a0003c0004t0001g0335a0003c0004t0001g0364others(6): Show | 9 | HG01517.hp2 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2616-633_2616-629d others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
G | GTTTTTT | 22 | a0001c0003t0006g0027a0003c0004t0001g0004a0003c0004t0001g0022others(19): Show | 23 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2616-634_2616-629d others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
G | GTTTTTTT | 19 | a0001c0003t0006g0026a0003c0004t0001g0332a0003c0004t0001g0333others(16): Show | 19 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2616-635_2616-629d others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
G | GTTTTTTT others(1): Show |
7 | a0003c0004t0001g0347a0003c0004t0001g0354a0003c0004t0001g0360others(4): Show | 7 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-636_2616-629d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
G | GTTTTTTT others(4): Show |
1 | a0003c0004t0001g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2616-639_2616-629d others(13): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
G | GTTTTTTT others(5): Show |
1 | a0003c0004t0001g0358 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2616-640_2616-629d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
GTTTTTTT | G | 25 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(22): Show | 25 | HG01069.hp2 HG01175.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.2616-635_2616-629d others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263744
|
GTTTTTTT others(1): Show |
G | 123 | a0001c0002t0003g0028a0001c0002t0003g0030a0002c0001t0002g0032others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.2616-636_2616-629d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | ||||||
| chr1:47263814
|
G | A | 1 | a0003c0004t0001g0023 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2616-698C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263814 | ||||||
| chr1:47263897
|
C | T | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2616-781G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263897 | ||||||
| chr1:47263965
|
C | G | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2616-849G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263965 | ||||||
| chr1:47264000
|
G | A | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-884C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264000 | ||||||
| chr1:47264016
|
G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2616-900C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264016 | ||||||
| chr1:47264040
|
A | C | 1 | a0003c0004t0001g0372 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2616-924T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264040 | ||||||
| chr1:47264213
|
C | T | 131 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2616-1097G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264213 | ||||||
| chr1:47264425
|
A | T | 1 | a0003c0004t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2616-1309T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264425 | ||||||
| chr1:47264473
|
C | T | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2616-1357G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264473 | ||||||
| chr1:47264505
|
A | T | 1 | a0002c0001t0002g0051 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2616-1389T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264505 | ||||||
| chr1:47264512
|
A | C | 69 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(66): Show | 70 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.2616-1396T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264512 | ||||||
| chr1:47264650
|
G | A | 34 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(31): Show | 34 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.2616-1534C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264650 | ||||||
| chr1:47264743
|
G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2616-1627C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264743 | ||||||
| chr1:47264786
|
T | C | 1 | a0001c0003t0001g0117 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2616-1670A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264786 | ||||||
| chr1:47264786
|
T | TAATCCAA others(6): Show |
2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2616-1683_2616-167 others(17): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264786 | ||||||
| chr1:47264930
|
T | TA | 103 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(100): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.2616-1815dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264930 | ||||||
| chr1:47264930
|
T | TAA | 117 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.2616-1816_2616-181 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264930 | ||||||
| chr1:47264930
|
TA | T | 66 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(63): Show | 67 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.2616-1815delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264930 | ||||||
| chr1:47264951
|
A | G | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616-1835T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264951 | ||||||
| chr1:47265002
|
G | A | 5 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(2): Show | 5 | HG02622.hp2 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2616-1886C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265002 | ||||||
| chr1:47265104
|
C | T | 34 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(31): Show | 34 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.2616-1988G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265104 | ||||||
| chr1:47265158
|
C | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2616-2042G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265158 | ||||||
| chr1:47265237
|
C | CA | 45 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(42): Show | 45 | HG00621.hp1 HG00639.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2616-2122dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAA | 11 | a0001c0002t0003g0017a0001c0002t0003g0227a0001c0002t0004g0211others(8): Show | 11 | HG01358.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2616-2123_2616-212 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAA | 25 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0010others(22): Show | 25 | HG00597.hp2 HG00738.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2616-2124_2616-212 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAA | 35 | a0001c0002t0003g0009a0001c0002t0003g0011a0001c0002t0003g0013others(32): Show | 36 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2616-2125_2616-212 others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAA | 7 | a0003c0004t0001g0334a0003c0004t0001g0338a0003c0004t0001g0343others(4): Show | 7 | HG00735.hp2 HG01106.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-2126_2616-212 others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA | 45 | a0002c0001t0002g0233a0002c0001t0002g0234a0002c0001t0002g0236others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.2616-2128_2616-212 others(11): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA others(1): Show |
37 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.2616-2129_2616-212 others(12): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA others(2): Show |
7 | a0002c0001t0002g0237a0002c0001t0002g0238a0002c0001t0002g0249others(4): Show | 7 | HG01192.hp1 HG01346.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-2130_2616-212 others(13): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA others(4): Show |
2 | a0004c0005t0002g0063a0004c0005t0002g0064 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2616-2132_2616-212 others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA others(5): Show |
5 | a0002c0001t0002g0035a0002c0001t0002g0037a0002c0001t0002g0046others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616-2133_2616-212 others(16): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA others(6): Show |
10 | a0002c0001t0002g0034a0002c0001t0002g0036a0002c0001t0002g0040others(7): Show | 10 | HG00673.hp2 HG02040.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.2616-2134_2616-212 others(17): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA others(7): Show |
7 | a0002c0001t0002g0041a0002c0001t0002g0043a0002c0001t0002g0048others(4): Show | 7 | HG01257.hp2 HG02056.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-2135_2616-212 others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA others(8): Show |
7 | a0002c0001t0002g0033a0002c0001t0002g0042a0002c0001t0002g0049others(4): Show | 7 | HG00280.hp2 HG00609.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2616-2136_2616-212 others(19): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265237
|
C | CAAAAAAA others(9): Show |
1 | a0002c0001t0002g0039 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2616-2137_2616-212 others(20): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | ||||||
| chr1:47265250
|
A | AC | 5 | a0001c0002t0001g0072a0001c0002t0001g0094a0001c0002t0001g0148others(2): Show | 5 | NA18947.hp2 NA18960.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616-2135_2616-213 others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265250 | ||||||
| chr1:47265250
|
A | C | 63 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(60): Show | 64 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.2616-2134T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265250 | ||||||
| chr1:47265252
|
A | AAAAAAAA others(3): Show |
1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2616-2137_2616-213 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265252 | ||||||
| chr1:47265257
|
A | AAAAAAAA others(6): Show |
2 | a0002c0001t0002g0054a0002c0001t0002g0059 | 2 | NA18944.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2616-2142_2616-214 others(17): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265257 | ||||||
| chr1:47265261
|
C | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2616-2145G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265261 | ||||||
| chr1:47265263
|
C | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2616-2147G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265263 | ||||||
| chr1:47265264
|
A | AAAAAAAA others(8): Show |
1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2616-2149_2616-214 others(19): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265264 | ||||||
| chr1:47265427
|
G | A | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-2311C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265427 | ||||||
| chr1:47265466
|
G | GT | 6 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2616-2351dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265466 | ||||||
| chr1:47265481
|
T | C | 1 | a0001c0002t0001g0165 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2616-2365A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265481 | ||||||
| chr1:47265637
|
C | T | 1 | a0001c0002t0001g0171 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2616-2521G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265637 | ||||||
| chr1:47265655
|
C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0095 | 2 | NA18992.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2616-2539G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265655 | ||||||
| chr1:47265716
|
G | T | 1 | a0002c0001t0002g0280 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2616-2600C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265716 | ||||||
| chr1:47265717
|
G | A | 1 | a0001c0002t0001g0172 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2616-2601C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265717 | ||||||
| chr1:47265783
|
C | CA | 39 | a0001c0002t0001g0067a0001c0002t0001g0078a0001c0002t0003g0013others(36): Show | 40 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2616-2668dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265783 | ||||||
| chr1:47265783
|
C | CAA | 122 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0071others(119): Show | 124 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.2616-2669_2616-266 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265783 | ||||||
| chr1:47265783
|
C | CAAA | 26 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0088others(23): Show | 26 | HG01109.hp2 HG02027.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.2616-2670_2616-266 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265783 | ||||||
| chr1:47265783
|
CA | C | 55 | a0001c0002t0003g0007a0001c0002t0004g0211a0001c0003t0006g0026others(52): Show | 56 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2616-2668delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265783 | ||||||
| chr1:47265786
|
A | G | 2 | a0003c0004t0001g0365a0003c0004t0001g0366 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2616-2670T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265786 | ||||||
| chr1:47265815
|
C | T | 4 | a0003c0004t0001g0375a0003c0004t0001g0376a0003c0004t0001g0377others(1): Show | 4 | HG02896.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616-2699G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265815 | ||||||
| chr1:47265829
|
C | T | 3 | a0001c0003t0001g0322a0001c0003t0001g0323a0001c0003t0001g0324 | 3 | HG02976.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2616-2713G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265829 | ||||||
| chr1:47265881
|
G | A | 3 | a0003c0004t0001g0354a0003c0004t0001g0357a0003c0004t0001g0358 | 3 | HG02109.hp2 HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2616-2765C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265881 | ||||||
| chr1:47265882
|
G | C | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-2766C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265882 | ||||||
| chr1:47266004
|
G | A | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2616-2888C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266004 | ||||||
| chr1:47266010
|
G | A | 19 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(16): Show | 19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2616-2894C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266010 | ||||||
| chr1:47266025
|
C | T | 2 | a0003c0004t0001g0024a0003c0004t0001g0025 | 2 | HG00642.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2616-2909G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266025 | ||||||
| chr1:47266462
|
G | C | 33 | a0002c0001t0002g0033a0002c0001t0002g0034a0002c0001t0002g0035others(30): Show | 33 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2615+3173C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266462 | ||||||
| chr1:47266495
|
A | G | 1 | a0001c0002t0001g0187 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2615+3140T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266495 | ||||||
| chr1:47266512
|
C | A | 11 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(8): Show | 11 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2615+3123G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266512 | ||||||
| chr1:47266529
|
G | A | 1 | a0001c0002t0003g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2615+3106C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266529 | ||||||
| chr1:47266590
|
C | G | 1 | a0001c0003t0001g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2615+3045G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266590 | ||||||
| chr1:47266617
|
G | T | 4 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2615+3018C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266617 | ||||||
| chr1:47266706
|
G | T | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2615+2929C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266706 | ||||||
| chr1:47266717
|
C | A | 1 | a0003c0004t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2615+2918G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266717 | ||||||
| chr1:47266753
|
A | T | 2 | a0001c0003t0001g0322a0001c0003t0001g0323 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2615+2882T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266753 | ||||||
| chr1:47266886
|
A | G | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2615+2749T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266886 | ||||||
| chr1:47267064
|
T | A | 11 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(8): Show | 11 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2615+2571A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267064 | ||||||
| chr1:47267116
|
G | T | 1 | a0001c0003t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2615+2519C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267116 | ||||||
| chr1:47267266
|
T | C | 26 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(23): Show | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.2615+2369A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267266 | ||||||
| chr1:47267358
|
C | T | 2 | a0001c0003t0001g0204a0001c0003t0001g0209 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2615+2277G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267358 | ||||||
| chr1:47267489
|
G | A | 1 | a0002c0001t0002g0282 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2615+2146C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267489 | ||||||
| chr1:47267522
|
T | G | 3 | a0001c0003t0001g0086a0001c0003t0001g0133a0001c0003t0001g0143 | 3 | NA18939.hp1 NA18961.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2615+2113A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267522 | ||||||
| chr1:47267565
|
T | A | 3 | a0001c0003t0001g0121a0001c0003t0001g0131a0001c0003t0001g0142 | 3 | NA18963.hp1 NA18977.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2615+2070A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267565 | ||||||
| chr1:47267583
|
T | G | 1 | a0001c0003t0001g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2615+2052A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267583 | ||||||
| chr1:47267617
|
G | A | 1 | a0001c0003t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2615+2018C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267617 | ||||||
| chr1:47267630
|
G | A | 64 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(61): Show | 64 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.2615+2005C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267630 | ||||||
| chr1:47267667
|
T | TA | 9 | a0001c0002t0001g0067a0001c0002t0001g0147a0001c0002t0001g0150others(6): Show | 9 | HG03516.hp1 HG03704.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.2615+1967dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267667 | ||||||
| chr1:47267667
|
T | TAA | 58 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0069others(55): Show | 59 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.2615+1966_2615+196 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267667 | ||||||
| chr1:47267667
|
TA | T | 206 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.2615+1967delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267667 | ||||||
| chr1:47267667
|
TAA | T | 14 | a0001c0002t0003g0006a0001c0002t0003g0014a0001c0002t0003g0015others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2615+1966_2615+196 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267667 | ||||||
| chr1:47267702
|
A | G | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2615+1933T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267702 | ||||||
| chr1:47267706
|
G | T | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2615+1929C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267706 | ||||||
| chr1:47267708
|
T | TTTTTG | 239 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(236): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2615+1922_2615+192 others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267708 | ||||||
| chr1:47267779
|
G | A | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2615+1856C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267779 | ||||||
| chr1:47267823
|
C | A | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2615+1812G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267823 | ||||||
| chr1:47267891
|
G | A | 32 | a0002c0001t0002g0033a0002c0001t0002g0034a0002c0001t0002g0035others(29): Show | 32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2615+1744C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267891 | ||||||
| chr1:47267919
|
G | GAAAATTT others(3): Show |
1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2615+1706_2615+171 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267919 | ||||||
| chr1:47268218
|
A | G | 1 | a0001c0002t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2615+1417T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268218 | ||||||
| chr1:47268267
|
G | A | 1 | a0001c0003t0001g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2615+1368C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268267 | ||||||
| chr1:47268476
|
T | C | 131 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2615+1159A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268476 | ||||||
| chr1:47268502
|
T | C | 224 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2615+1133A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268502 | ||||||
| chr1:47268512
|
T | C | 1 | a0001c0002t0001g0157 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2615+1123A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268512 | ||||||
| chr1:47268534
|
C | T | 1 | a0001c0002t0004g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2615+1101G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268534 | ||||||
| chr1:47268554
|
C | T | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2615+1081G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268554 | ||||||
| chr1:47268572
|
C | T | 224 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2615+1063G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268572 | ||||||
| chr1:47268713
|
G | A | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2615+922C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268713 | ||||||
| chr1:47268740
|
AAGAG | A | 5 | a0002c0001t0013g0062a0004c0005t0002g0063a0004c0005t0002g0064others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2615+891_2615+894d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268740 | ||||||
| chr1:47268755
|
T | C | 8 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2615+880A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268755 | ||||||
| chr1:47268758
|
C | CATAA | 12 | a0001c0002t0001g0072a0001c0002t0001g0090a0001c0002t0001g0149others(9): Show | 12 | HG01891.hp2 HG02040.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.2615+873_2615+876d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268758 | ||||||
| chr1:47268758
|
CATAA | C | 219 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.2615+873_2615+876d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268758 | ||||||
| chr1:47268758
|
CATAAATA others(1): Show |
C | 5 | a0001c0003t0001g0193a0001c0003t0001g0194a0001c0003t0001g0195others(2): Show | 5 | NA18942.hp2 NA18949.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2615+869_2615+876d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268758 | ||||||
| chr1:47268758
|
CATAAATA others(9): Show |
C | 1 | a0002c0001t0002g0243 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2615+861_2615+876d others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268758 | ||||||
| chr1:47268773
|
A | T | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2615+862T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268773 | ||||||
| chr1:47268777
|
A | T | 7 | a0001c0002t0003g0006a0001c0002t0003g0014a0001c0002t0003g0015others(4): Show | 7 | HG01069.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2615+858T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268777 | ||||||
| chr1:47268781
|
A | T | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(29): Show | 32 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.2615+854T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268781 | ||||||
| chr1:47268782
|
A | G | 12 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0115others(9): Show | 12 | HG03491.hp1 HG03492.hp2 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.2615+853T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268782 | ||||||
| chr1:47268785
|
A | T | 70 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(67): Show | 70 | HG00597.hp2 HG00735.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.2615+850T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268785 | ||||||
| chr1:47268789
|
A | T | 94 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(91): Show | 95 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.2615+846T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268789 | ||||||
| chr1:47268890
|
G | A | 1 | a0002c0001t0002g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2615+745C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268890 | ||||||
| chr1:47268991
|
G | GGAGGCT | 131 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2615+643_2615+644i others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268991 | ||||||
| chr1:47269013
|
C | T | 2 | a0002c0001t0002g0040a0002c0001t0002g0046 | 2 | HG00673.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2615+622G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269013 | ||||||
| chr1:47269078
|
G | A | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2615+557C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269078 | ||||||
| chr1:47269088
|
C | CA | 29 | a0001c0002t0001g0069a0001c0002t0001g0158a0001c0002t0001g0159others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.2615+546dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269088 | ||||||
| chr1:47269088
|
CA | C | 16 | a0001c0002t0001g0067a0001c0002t0001g0188a0001c0003t0001g0003others(13): Show | 17 | HG00597.hp1 HG00639.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2615+546delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269088 | ||||||
| chr1:47269111
|
C | T | 1 | a0002c0001t0002g0236 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2615+524G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269111 | ||||||
| chr1:47269175
|
T | G | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2615+460A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269175 | ||||||
| chr1:47269183
|
T | A | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2615+452A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269183 | ||||||
| chr1:47269370
|
C | CA | 6 | a0001c0002t0001g0073a0003c0004t0001g0354a0003c0004t0001g0355others(3): Show | 6 | HG00597.hp2 HG02109.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.2615+264dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269370 | ||||||
| chr1:47269589
|
A | T | 1 | a0001c0003t0001g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2615+46T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269589 | ||||||
| chr1:47269590
|
T | A | 1 | a0003c0004t0001g0373 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2615+45A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269590 | ||||||
| chr1:47269608
|
T | C | 131 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2615+27A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269608 | ||||||
| chr1:47269879
|
T | C | 7 | a0002c0001t0002g0052a0002c0001t0002g0060a0002c0001t0002g0383others(4): Show | 7 | HG00280.hp2 HG02132.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.2384-13A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47269879 | ||||||
| chr1:47270062
|
T | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2384-196A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270062 | ||||||
| chr1:47270063
|
C | T | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2384-197G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270063 | ||||||
| chr1:47270101
|
T | G | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2384-235A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270101 | ||||||
| chr1:47270102
|
G | T | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2384-236C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270102 | ||||||
| chr1:47270227
|
CA | C | 60 | a0001c0002t0003g0014a0002c0001t0002g0033a0002c0001t0002g0034others(57): Show | 60 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2384-362delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270227 | ||||||
| chr1:47270227
|
CAA | C | 36 | a0003c0004t0001g0004a0003c0004t0001g0023a0003c0004t0001g0024others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.2384-363_2384-362d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270227 | ||||||
| chr1:47270227
|
CAAA | C | 11 | a0001c0002t0003g0021a0002c0001t0002g0032a0002c0001t0002g0060others(8): Show | 11 | HG00099.hp2 HG03130.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.2384-364_2384-362d others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270227 | ||||||
| chr1:47270233
|
A | AAT | 8 | a0001c0003t0001g0003a0001c0003t0001g0217a0001c0003t0001g0219others(5): Show | 9 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2384-368_2384-367i others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270233 | ||||||
| chr1:47270235
|
A | T | 13 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(10): Show | 14 | HG00639.hp2 HG01891.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2384-369T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270235 | ||||||
| chr1:47270237
|
A | T | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2384-371T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270237 | ||||||
| chr1:47270239
|
A | AT | 33 | a0002c0001t0002g0238a0002c0001t0002g0239a0002c0001t0002g0244others(30): Show | 33 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.2384-374_2384-373i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270239 | ||||||
| chr1:47270239
|
A | ATAT | 14 | a0002c0001t0002g0236a0002c0001t0002g0240a0002c0001t0002g0247others(11): Show | 14 | HG00597.hp1 HG01074.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2384-374_2384-373i others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270239 | ||||||
| chr1:47270239
|
A | T | 25 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(22): Show | 26 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2384-373T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270239 | ||||||
| chr1:47270240
|
AAATAT | A | 11 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(8): Show | 11 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2384-379_2384-375d others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270240 | ||||||
| chr1:47270241
|
A | AT | 8 | a0001c0002t0001g0149a0001c0002t0001g0180a0001c0002t0003g0015others(5): Show | 8 | HG02083.hp2 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384-376_2384-375i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270241 | ||||||
| chr1:47270241
|
A | ATAT | 4 | a0001c0002t0001g0093a0001c0003t0001g0189a0001c0003t0001g0194others(1): Show | 4 | HG01346.hp2 HG01515.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2384-376_2384-375i others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270241 | ||||||
| chr1:47270241
|
A | T | 131 | a0001c0002t0001g0099a0001c0002t0001g0166a0001c0002t0001g0179others(128): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.2384-375T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270241 | ||||||
| chr1:47270243
|
T | A | 3 | a0001c0002t0001g0091a0005c0007t0004g0213a0005c0007t0004g0214 | 3 | HG00673.hp1 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2384-377A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270243 | ||||||
| chr1:47270247
|
T | C | 14 | a0001c0002t0003g0015a0001c0002t0003g0016a0002c0001t0002g0236others(11): Show | 14 | HG00597.hp1 HG01074.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2384-381A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270247 | ||||||
| chr1:47270247
|
T | TACAC | 3 | a0002c0001t0002g0280a0002c0001t0002g0299a0002c0001t0002g0305 | 3 | HG01496.hp1 HG03710.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.2384-382_2384-381i others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270247 | ||||||
| chr1:47270247
|
TATATATA others(9): Show |
T | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2384-397_2384-382d others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270247 | ||||||
| chr1:47270249
|
T | C | 54 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.2384-383A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270249 | ||||||
| chr1:47270249
|
T | TACACAC | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2384-384_2384-383i others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270249 | ||||||
| chr1:47270251
|
T | C | 108 | a0001c0002t0001g0076a0001c0002t0003g0007a0001c0002t0003g0008others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.2384-385A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270251 | ||||||
| chr1:47270251
|
TATATACA others(5): Show |
T | 1 | a0001c0003t0001g0109 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2384-397_2384-386d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270251 | ||||||
| chr1:47270253
|
T | C | 158 | a0001c0002t0001g0071a0001c0002t0001g0073a0001c0002t0001g0076others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2384-387A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270253 | ||||||
| chr1:47270253
|
T | TAC | 41 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(38): Show | 42 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.2384-388_2384-387i others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270253 | ||||||
| chr1:47270253
|
T | TACAC | 7 | a0001c0002t0001g0088a0001c0002t0001g0150a0001c0002t0001g0166others(4): Show | 7 | HG01109.hp2 HG02004.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.2384-388_2384-387i others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270253 | ||||||
| chr1:47270253
|
TATACACA others(5): Show |
T | 3 | a0001c0003t0001g0080a0001c0003t0001g0081a0001c0003t0001g0082 | 3 | HG01109.hp1 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2384-399_2384-388d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270253 | ||||||
| chr1:47270255
|
T | C | 219 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.2384-389A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270255
|
T | TAC | 15 | a0001c0002t0001g0152a0001c0003t0001g0105a0001c0003t0001g0112others(12): Show | 15 | HG00735.hp1 HG01167.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2384-391_2384-390d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270255
|
T | TACAC | 46 | a0001c0003t0001g0074a0001c0003t0001g0079a0001c0003t0001g0084others(43): Show | 46 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.2384-393_2384-390d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270255
|
T | TACACAC | 10 | a0001c0002t0004g0228a0001c0003t0001g0001a0001c0003t0001g0086others(7): Show | 11 | HG02027.hp1 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2384-395_2384-390d others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270255
|
T | TACACACA others(1): Show |
6 | a0001c0003t0001g0139a0001c0003t0001g0140a0001c0003t0001g0322others(3): Show | 6 | HG02735.hp2 HG02976.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384-397_2384-390d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270255
|
TAC | T | 7 | a0001c0003t0001g0331a0003c0004t0001g0022a0003c0004t0001g0031others(4): Show | 7 | HG00597.hp2 HG01175.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2384-391_2384-390d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270255
|
TACAC | T | 6 | a0003c0004t0001g0332a0003c0004t0001g0335a0003c0004t0001g0337others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384-393_2384-390d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270255
|
TACACACA others(3): Show |
T | 1 | a0002c0001t0002g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2384-399_2384-390d others(12): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270255
|
TACACACA others(5): Show |
T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2384-401_2384-390d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | ||||||
| chr1:47270257
|
C | T | 43 | a0001c0002t0004g0211a0001c0002t0004g0229a0001c0002t0004g0230others(40): Show | 44 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2384-391G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270257 | ||||||
| chr1:47270259
|
C | T | 3 | a0003c0004t0001g0336a0003c0004t0001g0343a0003c0004t0001g0372 | 3 | HG01516.hp1 HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2384-393G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270259 | ||||||
| chr1:47270263
|
C | T | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2384-397G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270263 | ||||||
| chr1:47270388
|
C | A | 9 | a0001c0002t0001g0070a0001c0002t0001g0156a0001c0002t0001g0157others(6): Show | 9 | NA18960.hp1 NA18964.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2384-522G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270388 | ||||||
| chr1:47270389
|
G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2384-523C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270389 | ||||||
| chr1:47270478
|
C | T | 1 | a0002c0001t0015g0388 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2384-612G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270478 | ||||||
| chr1:47270644
|
T | C | 2 | a0001c0002t0001g0002a0001c0002t0001g0094 | 3 | NA18950.hp1 NA19010.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2384-778A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270644 | ||||||
| chr1:47270668
|
A | C | 1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2384-802T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270668 | ||||||
| chr1:47270670
|
C | CT | 44 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0093others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2384-805dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | ||||||
| chr1:47270670
|
C | CTT | 81 | a0002c0001t0002g0032a0002c0001t0002g0051a0002c0001t0002g0061others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.2384-806_2384-805d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | ||||||
| chr1:47270670
|
C | CTTT | 13 | a0001c0003t0001g0120a0001c0003t0001g0123a0001c0003t0001g0124others(10): Show | 13 | HG00621.hp2 HG01175.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.2384-807_2384-805d others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | ||||||
| chr1:47270670
|
C | T | 1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2384-804G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | ||||||
| chr1:47270670
|
CT | C | 36 | a0001c0002t0001g0070a0001c0002t0001g0072a0001c0002t0001g0076others(33): Show | 36 | HG01069.hp2 HG01167.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.2384-805delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | ||||||
| chr1:47270670
|
CTT | C | 7 | a0001c0002t0003g0227a0001c0002t0003g0325a0001c0002t0003g0326others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2384-806_2384-805d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | ||||||
| chr1:47270670
|
CTTTTT | C | 57 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(54): Show | 58 | HG00099.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.2384-809_2384-805d others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | ||||||
| chr1:47270747
|
A | G | 240 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.2384-881T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270747 | ||||||
| chr1:47270775
|
C | T | 19 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(16): Show | 19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2384-909G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270775 | ||||||
| chr1:47270816
|
C | T | 69 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(66): Show | 70 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.2384-950G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270816 | ||||||
| chr1:47270823
|
T | A | 1 | a0002c0001t0002g0312 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2384-957A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270823 | ||||||
| chr1:47270827
|
C | G | 1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2384-961G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270827 | ||||||
| chr1:47270828
|
G | C | 1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2384-962C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270828 | ||||||
| chr1:47270898
|
C | T | 3 | a0001c0002t0003g0011a0001c0003t0006g0026a0001c0003t0006g0027 | 3 | HG02486.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2384-1032G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270898 | ||||||
| chr1:47271060
|
A | T | 9 | a0001c0002t0001g0070a0001c0002t0001g0156a0001c0002t0001g0157others(6): Show | 9 | NA18960.hp1 NA18964.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2383+1016T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271060 | ||||||
| chr1:47271141
|
T | C | 1 | a0003c0004t0001g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2383+935A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271141 | ||||||
| chr1:47271290
|
T | G | 1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2383+786A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271290 | ||||||
| chr1:47271311
|
G | A | 67 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(64): Show | 68 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.2383+765C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271311 | ||||||
| chr1:47271317
|
C | T | 224 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2383+759G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271317 | ||||||
| chr1:47271432
|
T | G | 1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2383+644A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271432 | ||||||
| chr1:47271434
|
T | A | 1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2383+642A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271434 | ||||||
| chr1:47271490
|
C | T | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2383+586G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271490 | ||||||
| chr1:47271541
|
G | A | 1 | a0002c0001t0002g0037 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2383+535C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271541 | ||||||
| chr1:47271546
|
G | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2383+530C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271546 | ||||||
| chr1:47271558
|
C | CA | 10 | a0001c0002t0001g0073a0001c0002t0001g0203a0001c0002t0003g0013others(7): Show | 10 | HG00738.hp2 HG02486.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2383+517dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271558 | ||||||
| chr1:47271558
|
CA | C | 134 | a0001c0002t0001g0202a0001c0003t0001g0111a0001c0003t0001g0116others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.2383+517delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271558 | ||||||
| chr1:47271574
|
A | G | 1 | a0002c0001t0002g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2383+502T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271574 | ||||||
| chr1:47271701
|
G | C | 1 | a0003c0004t0001g0345 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2383+375C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271701 | ||||||
| chr1:47271802
|
C | T | 19 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(16): Show | 19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2383+274G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271802 | ||||||
| chr1:47271813
|
A | C | 64 | a0001c0003t0006g0026a0001c0003t0006g0027a0002c0001t0013g0062others(61): Show | 65 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2383+263T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271813 | ||||||
| chr1:47271819
|
A | C | 3 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016 | 3 | HG01069.hp2 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2383+257T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271819 | ||||||
| chr1:47271820
|
C | A | 1 | a0002c0001t0002g0261 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2383+256G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271820 | ||||||
| chr1:47271821
|
A | C | 1 | a0002c0001t0002g0261 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2383+255T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271821 | ||||||
| chr1:47271838
|
C | A | 4 | a0001c0002t0003g0017a0001c0002t0004g0229a0001c0002t0004g0230others(1): Show | 4 | HG01884.hp1 HG02145.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2383+238G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271838 | ||||||
| chr1:47271965
|
T | C | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2383+111A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271965 | ||||||
| chr1:47272258
|
C | T | 32 | a0002c0001t0002g0033a0002c0001t0002g0034a0002c0001t0002g0035others(29): Show | 32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2218-17G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272258 | ||||||
| chr1:47272390
|
A | G | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2218-149T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272390 | ||||||
| chr1:47272448
|
AT | A | 166 | a0001c0002t0003g0227a0002c0001t0002g0032a0002c0001t0002g0033others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.2218-208delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272448 | ||||||
| chr1:47272448
|
ATT | A | 21 | a0003c0004t0001g0004a0003c0004t0001g0031a0003c0004t0001g0332others(18): Show | 22 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.2218-209_2218-208d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272448 | ||||||
| chr1:47272524
|
T | C | 1 | a0001c0003t0001g0190 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2218-283A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272524 | ||||||
| chr1:47272551
|
C | T | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2218-310G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272551 | ||||||
| chr1:47272598
|
C | CACCACCA others(48): Show |
1 | a0002c0001t0002g0043 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2218-412_2218-358d others(57): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272598 | ||||||
| chr1:47272978
|
C | T | 4 | a0003c0004t0001g0375a0003c0004t0001g0376a0003c0004t0001g0377others(1): Show | 4 | HG02896.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2218-737G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272978 | ||||||
| chr1:47272979
|
A | G | 56 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(53): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2218-738T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272979 | ||||||
| chr1:47273025
|
T | C | 1 | a0001c0003t0010g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2218-784A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273025 | ||||||
| chr1:47273102
|
G | A | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2218-861C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273102 | ||||||
| chr1:47273269
|
G | A | 1 | a0001c0003t0001g0190 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2218-1028C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273269 | ||||||
| chr1:47273285
|
T | C | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2218-1044A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273285 | ||||||
| chr1:47273408
|
C | T | 1 | a0001c0003t0001g0126 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2218-1167G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273408 | ||||||
| chr1:47273569
|
G | T | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2218-1328C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273569 | ||||||
| chr1:47273640
|
G | A | 2 | a0003c0004t0001g0347a0003c0004t0001g0348 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2218-1399C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273640 | ||||||
| chr1:47273705
|
G | A | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2218-1464C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273705 | ||||||
| chr1:47273761
|
C | T | 19 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0108others(16): Show | 19 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.2218-1520G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273761 | ||||||
| chr1:47273789
|
A | G | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2218-1548T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273789 | ||||||
| chr1:47273793
|
T | A | 1 | a0001c0003t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2218-1552A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273793 | ||||||
| chr1:47273989
|
T | C | 6 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2218-1748A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273989 | ||||||
| chr1:47274030
|
T | C | 1 | a0001c0002t0001g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2218-1789A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274030 | ||||||
| chr1:47274095
|
TAC | T | 240 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.2218-1856_2218-185 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274095 | ||||||
| chr1:47274105
|
C | G | 2 | a0001c0002t0001g0069a0001c0002t0001g0173 | 2 | NA18974.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2218-1864G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274105 | ||||||
| chr1:47274120
|
T | C | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2218-1879A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274120 | ||||||
| chr1:47274220
|
A | G | 1 | a0003c0004t0001g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2218-1979T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274220 | ||||||
| chr1:47274371
|
G | A | 1 | a0002c0001t0002g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2218-2130C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274371 | ||||||
| chr1:47274455
|
C | T | 35 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(32): Show | 35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2218-2214G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274455 | ||||||
| chr1:47274471
|
C | T | 1 | a0001c0003t0001g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2218-2230G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274471 | ||||||
| chr1:47274613
|
A | G | 228 | a0001c0002t0001g0067a0001c0002t0001g0167a0001c0002t0001g0168others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2218-2372T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274613 | ||||||
| chr1:47274730
|
A | C | 1 | a0011c0018t0008g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2218-2489T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274730 | ||||||
| chr1:47274766
|
T | C | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2218-2525A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274766 | ||||||
| chr1:47274777
|
G | C | 2 | a0001c0002t0001g0071a0001c0002t0001g0200 | 2 | NA18995.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2218-2536C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274777 | ||||||
| chr1:47274807
|
CT | C | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2218-2567delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274807 | ||||||
| chr1:47274851
|
C | T | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2218-2610G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274851 | ||||||
| chr1:47274975
|
A | C | 1 | a0002c0001t0002g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2218-2734T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274975 | ||||||
| chr1:47275009
|
G | A | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2218-2768C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275009 | ||||||
| chr1:47275076
|
T | C | 310 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2218-2835A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275076 | ||||||
| chr1:47275147
|
T | TCAA | 238 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.2218-2909_2218-290 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275147 | ||||||
| chr1:47275189
|
G | A | 2 | a0001c0002t0004g0228a0003c0004t0001g0359 | 2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2218-2948C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275189 | ||||||
| chr1:47275201
|
G | A | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2218-2960C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275201 | ||||||
| chr1:47275240
|
T | A | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2218-2999A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275240 | ||||||
| chr1:47275292
|
G | A | 8 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(5): Show | 8 | HG00642.hp1 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2218-3051C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275292 | ||||||
| chr1:47275292
|
G | T | 1 | a0001c0003t0001g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2218-3051C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275292 | ||||||
| chr1:47275351
|
G | C | 1 | a0003c0004t0001g0022 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2218-3110C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275351 | ||||||
| chr1:47275400
|
A | T | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2218-3159T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275400 | ||||||
| chr1:47275466
|
G | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2218-3225C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275466 | ||||||
| chr1:47275485
|
G | A | 35 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(32): Show | 35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2218-3244C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275485 | ||||||
| chr1:47275630
|
A | AT | 17 | a0001c0003t0001g0003a0001c0003t0001g0131a0001c0003t0001g0216others(14): Show | 18 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2218-3390dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275630 | ||||||
| chr1:47275661
|
G | C | 7 | a0001c0002t0003g0227a0001c0002t0003g0325a0001c0002t0003g0326others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2218-3420C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275661 | ||||||
| chr1:47275664
|
G | A | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2218-3423C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275664 | ||||||
| chr1:47275676
|
G | C | 56 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(53): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2218-3435C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275676 | ||||||
| chr1:47275687
|
C | T | 1 | a0001c0002t0003g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2218-3446G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275687 | ||||||
| chr1:47275760
|
G | A | 1 | a0001c0003t0010g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2218-3519C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275760 | ||||||
| chr1:47275848
|
T | A | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2218-3607A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275848 | ||||||
| chr1:47275920
|
C | A | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2218-3679G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275920 | ||||||
| chr1:47276001
|
A | G | 8 | a0003c0004t0001g0369a0003c0004t0001g0371a0003c0004t0001g0372others(5): Show | 8 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.2218-3760T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276001 | ||||||
| chr1:47276002
|
C | CT | 215 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2218-3762dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276002 | ||||||
| chr1:47276027
|
G | A | 35 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(32): Show | 35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2218-3786C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276027 | ||||||
| chr1:47276051
|
G | A | 1 | a0001c0002t0001g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3810C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276051 | ||||||
| chr1:47276052
|
G | C | 1 | a0001c0002t0001g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3811C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276052 | ||||||
| chr1:47276054
|
G | C | 1 | a0001c0002t0001g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3813C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276054 | ||||||
| chr1:47276056
|
G | A | 1 | a0001c0002t0001g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3815C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276056 | ||||||
| chr1:47276057
|
C | G | 1 | a0001c0002t0001g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3816G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276057 | ||||||
| chr1:47276061
|
G | C | 1 | a0001c0002t0001g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3820C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276061 | ||||||
| chr1:47276063
|
T | C | 1 | a0001c0002t0001g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3822A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276063 | ||||||
| chr1:47276066
|
G | T | 1 | a0001c0003t0001g0192 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2218-3825C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276066 | ||||||
| chr1:47276067
|
A | T | 1 | a0001c0002t0001g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3826T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276067 | ||||||
| chr1:47276097
|
G | A | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2218-3856C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276097 | ||||||
| chr1:47276183
|
G | A | 1 | a0002c0001t0002g0033 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2218-3942C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276183 | ||||||
| chr1:47276249
|
G | A | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2217+3992C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276249 | ||||||
| chr1:47276307
|
T | G | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2217+3934A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276307 | ||||||
| chr1:47276396
|
G | A | 1 | a0003c0004t0001g0374 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2217+3845C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276396 | ||||||
| chr1:47276415
|
C | CAT | 3 | a0001c0002t0001g0179a0001c0003t0001g0128a0010c0019t0001g0177 | 3 | HG02602.hp1 HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2217+3824_2217+382 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276415 | ||||||
| chr1:47276415
|
CAT | C | 3 | a0003c0004t0001g0380a0003c0004t0001g0381a0003c0004t0001g0382 | 3 | HG02922.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2217+3824_2217+382 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276415 | ||||||
| chr1:47276431
|
A | C | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2217+3810T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276431 | ||||||
| chr1:47276584
|
G | T | 2 | a0002c0001t0002g0238a0002c0001t0002g0280 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2217+3657C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276584 | ||||||
| chr1:47276589
|
C | T | 56 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(53): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2217+3652G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276589 | ||||||
| chr1:47276600
|
G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2217+3641C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276600 | ||||||
| chr1:47276735
|
G | A | 1 | a0008c0012t0002g0297 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2217+3506C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276735 | ||||||
| chr1:47276744
|
A | G | 310 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2217+3497T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276744 | ||||||
| chr1:47276812
|
T | TA | 54 | a0001c0002t0001g0068a0001c0002t0001g0071a0001c0002t0001g0076others(51): Show | 54 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.2217+3428dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | ||||||
| chr1:47276812
|
TA | T | 46 | a0001c0002t0001g0077a0001c0002t0001g0148a0001c0002t0004g0231others(43): Show | 46 | HG00408.hp1 HG00738.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2217+3428delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | ||||||
| chr1:47276812
|
TAA | T | 73 | a0001c0002t0004g0211a0001c0002t0004g0229a0001c0003t0001g0216others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.2217+3427_2217+342 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | ||||||
| chr1:47276812
|
TAAA | T | 64 | a0001c0002t0003g0010a0001c0002t0003g0016a0001c0002t0003g0019others(61): Show | 65 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2217+3426_2217+342 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | ||||||
| chr1:47276812
|
TAAAA | T | 59 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2217+3425_2217+342 others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | ||||||
| chr1:47276814
|
A | T | 2 | a0002c0001t0002g0240a0002c0001t0002g0257 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2217+3427T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276814 | ||||||
| chr1:47276828
|
A | C | 1 | a0001c0003t0001g0115 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2217+3413T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276828 | ||||||
| chr1:47277036
|
T | C | 3 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030 | 3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2217+3205A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277036 | ||||||
| chr1:47277054
|
T | C | 130 | a0002c0001t0002g0032a0002c0001t0002g0033a0002c0001t0002g0034others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2217+3187A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277054 | ||||||
| chr1:47277241
|
G | C | 3 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030 | 3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2217+3000C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277241 | ||||||
| chr1:47277480
|
C | T | 4 | a0002c0001t0002g0259a0002c0001t0002g0265a0002c0001t0002g0266others(1): Show | 4 | HG00738.hp1 HG01433.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217+2761G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277480 | ||||||
| chr1:47277491
|
G | A | 9 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2217+2750C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277491 | ||||||
| chr1:47277506
|
A | C | 2 | a0003c0004t0001g0355a0003c0004t0001g0356 | 2 | HG00597.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2217+2735T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277506 | ||||||
| chr1:47277517
|
C | A | 32 | a0002c0001t0002g0033a0002c0001t0002g0034a0002c0001t0002g0035others(29): Show | 32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2217+2724G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277517 | ||||||
| chr1:47277712
|
A | C | 1 | a0001c0002t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2217+2529T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277712 | ||||||
| chr1:47277818
|
C | T | 29 | a0002c0001t0002g0233a0002c0001t0002g0234a0002c0001t0002g0235others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.2217+2423G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277818 | ||||||
| chr1:47277987
|
C | T | 3 | a0005c0007t0004g0213a0005c0007t0004g0214a0005c0017t0004g0215 | 3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2217+2254G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277987 | ||||||
| chr1:47278153
|
T | C | 147 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2217+2088A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278153 | ||||||
| chr1:47278222
|
T | C | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2217+2019A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278222 | ||||||
| chr1:47278247
|
T | C | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2217+1994A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278247 | ||||||
| chr1:47278286
|
C | A | 1 | a0002c0001t0002g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2217+1955G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278286 | ||||||
| chr1:47278302
|
T | G | 387 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(384): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.2217+1939A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278302 | ||||||
| chr1:47278375
|
T | C | 1 | a0001c0002t0003g0015 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2217+1866A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278375 | ||||||
| chr1:47278541
|
G | A | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.2217+1700C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278541 | ||||||
| chr1:47278645
|
A | T | 1 | a0002c0001t0002g0043 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2217+1596T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278645 | ||||||
| chr1:47278648
|
G | A | 4 | a0003c0004t0001g0371a0003c0004t0001g0372a0003c0015t0001g0367others(1): Show | 4 | HG00738.hp2 HG03710.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217+1593C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278648 | ||||||
| chr1:47278742
|
G | A | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2217+1499C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278742 | ||||||
| chr1:47278752
|
G | A | 1 | a0002c0001t0002g0386 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2217+1489C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278752 | ||||||
| chr1:47278785
|
G | A | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2217+1456C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278785 | ||||||
| chr1:47278821
|
T | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2217+1420A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278821 | ||||||
| chr1:47278822
|
A | T | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2217+1419T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278822 | ||||||
| chr1:47278881
|
CTAAATTT others(128): Show |
C | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1225_2217+135 others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278881 | ||||||
| chr1:47278991
|
A | G | 2 | a0001c0003t0001g0111a0001c0003t0001g0114 | 2 | HG01168.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2217+1250T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278991 | ||||||
| chr1:47279028
|
A | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1213T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279028 | ||||||
| chr1:47279049
|
A | G | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1192T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279049 | ||||||
| chr1:47279060
|
G | A | 5 | a0002c0001t0013g0062a0004c0005t0002g0063a0004c0005t0002g0064others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2217+1181C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279060 | ||||||
| chr1:47279068
|
T | C | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1173A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279068 | ||||||
| chr1:47279072
|
A | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1169T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279072 | ||||||
| chr1:47279079
|
C | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1162G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279079 | ||||||
| chr1:47279080
|
A | G | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1161T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279080 | ||||||
| chr1:47279093
|
C | G | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2217+1148G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279093 | ||||||
| chr1:47279118
|
A | C | 26 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(23): Show | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.2217+1123T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279118 | ||||||
| chr1:47279199
|
C | T | 4 | a0002c0001t0002g0237a0002c0001t0002g0261a0002c0001t0002g0267others(1): Show | 4 | HG01361.hp2 HG02683.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217+1042G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279199 | ||||||
| chr1:47279278
|
G | A | 1 | a0001c0002t0003g0011 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2217+963C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279278 | ||||||
| chr1:47279282
|
C | CA | 8 | a0001c0002t0001g0166a0001c0003t0001g0106a0001c0003t0001g0135others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.2217+958dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279282 | ||||||
| chr1:47279282
|
CA | C | 120 | a0001c0002t0001g0099a0001c0002t0001g0179a0001c0003t0001g0003others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.2217+958delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279282 | ||||||
| chr1:47279299
|
AAT | A | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(29): Show | 32 | HG01069.hp2 HG01884.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.2217+940_2217+941d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279299 | ||||||
| chr1:47279301
|
T | A | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2217+940A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279301 | ||||||
| chr1:47279418
|
T | C | 1 | a0001c0002t0003g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2217+823A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279418 | ||||||
| chr1:47279706
|
G | A | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2217+535C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279706 | ||||||
| chr1:47279726
|
T | A | 1 | a0001c0002t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2217+515A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279726 | ||||||
| chr1:47279727
|
C | A | 1 | a0001c0002t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2217+514G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279727 | ||||||
| chr1:47279727
|
C | CA | 102 | a0001c0002t0001g0072a0001c0002t0001g0089a0001c0002t0001g0179others(99): Show | 103 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.2217+513dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279727 | ||||||
| chr1:47279727
|
C | CAA | 28 | a0001c0002t0003g0006a0001c0002t0003g0013a0001c0002t0003g0016others(25): Show | 29 | HG00639.hp2 HG01891.hp1 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.2217+512_2217+513d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279727 | ||||||
| chr1:47279727
|
CA | C | 6 | a0001c0002t0001g0149a0001c0002t0001g0150a0001c0002t0001g0172others(3): Show | 6 | HG01168.hp1 NA18947.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2217+513delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279727 | ||||||
| chr1:47279740
|
A | C | 1 | a0002c0001t0002g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2217+501T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279740 | ||||||
| chr1:47279746
|
C | A | 11 | a0001c0002t0003g0012a0001c0002t0003g0013a0001c0002t0004g0211others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2217+495G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279746 | ||||||
| chr1:47279749
|
C | A | 1 | a0001c0002t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2217+492G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279749 | ||||||
| chr1:47279834
|
T | C | 147 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2217+407A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279834 | ||||||
| chr1:47279836
|
C | T | 1 | a0002c0001t0005g0273 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2217+405G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279836 | ||||||
| chr1:47279972
|
A | C | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2217+269T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279972 | ||||||
| chr1:47280088
|
G | A | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2217+153C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47280088 | ||||||
| chr1:47281321
|
G | A | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1249-112C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47281321 | ||||||
| chr1:47281418
|
T | C | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1249-209A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47281418 | ||||||
| chr1:47281483
|
A | G | 1 | a0002c0001t0002g0305 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1249-274T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47281483 | ||||||
| chr1:47281773
|
G | A | 256 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(253): Show | 260 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.1249-564C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47281773 | ||||||
| chr1:47282239
|
T | C | 1 | a0001c0003t0010g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1248+106A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47282239 | ||||||
| chr1:47282480
|
C | G | 1 | a0001c0003t0001g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1134-21G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47282480 | ||||||
| chr1:47282571
|
T | A | 7 | a0002c0001t0002g0256a0002c0001t0002g0271a0002c0001t0002g0290others(4): Show | 7 | NA18939.hp2 NA18955.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134-112A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47282571 | ||||||
| chr1:47282892
|
A | G | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134-433T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47282892 | ||||||
| chr1:47282958
|
A | G | 1 | a0002c0001t0002g0249 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1134-499T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47282958 | ||||||
| chr1:47283180
|
G | C | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1134-721C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283180 | ||||||
| chr1:47283279
|
T | C | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1134-820A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283279 | ||||||
| chr1:47283581
|
T | C | 1 | a0002c0001t0002g0272 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1134-1122A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283581 | ||||||
| chr1:47283729
|
C | T | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.1134-1270G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283729 | ||||||
| chr1:47283921
|
T | C | 2 | a0001c0002t0001g0077a0001c0002t0001g0078 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1134-1462A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283921 | ||||||
| chr1:47283922
|
A | G | 26 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(23): Show | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1134-1463T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283922 | ||||||
| chr1:47283972
|
C | T | 1 | a0001c0003t0001g0110 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1134-1513G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283972 | ||||||
| chr1:47283981
|
C | T | 1 | a0001c0002t0001g0171 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1134-1522G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283981 | ||||||
| chr1:47283985
|
G | A | 1 | a0002c0001t0002g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1134-1526C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283985 | ||||||
| chr1:47284061
|
C | A | 1 | a0001c0002t0003g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1134-1602G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284061 | ||||||
| chr1:47284259
|
T | C | 147 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1134-1800A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284259 | ||||||
| chr1:47284514
|
T | C | 2 | a0001c0002t0004g0229a0001c0002t0004g0230 | 2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1134-2055A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284514 | ||||||
| chr1:47284596
|
A | G | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.1134-2137T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284596 | ||||||
| chr1:47284608
|
G | C | 16 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(13): Show | 16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1134-2149C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284608 | ||||||
| chr1:47284640
|
A | T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1134-2181T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284640 | ||||||
| chr1:47284713
|
A | G | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134-2254T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284713 | ||||||
| chr1:47284879
|
G | GA | 19 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(16): Show | 19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1134-2421dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284879 | ||||||
| chr1:47284889
|
C | CA | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(29): Show | 32 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.1134-2431dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284889 | ||||||
| chr1:47285020
|
C | CT | 98 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(95): Show | 100 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1133+2530dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285020 | ||||||
| chr1:47285020
|
C | CTTT | 147 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0069others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1133+2528_1133+253 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285020 | ||||||
| chr1:47285087
|
G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1133+2464C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285087 | ||||||
| chr1:47285256
|
T | G | 1 | a0003c0004t0001g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1133+2295A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285256 | ||||||
| chr1:47285340
|
T | A | 21 | a0003c0004t0001g0004a0003c0004t0001g0031a0003c0004t0001g0332others(18): Show | 22 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1133+2211A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285340 | ||||||
| chr1:47285448
|
A | T | 11 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(8): Show | 11 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1133+2103T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285448 | ||||||
| chr1:47285618
|
C | T | 5 | a0002c0001t0013g0062a0004c0005t0002g0063a0004c0005t0002g0064others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1133+1933G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285618 | ||||||
| chr1:47285647
|
G | A | 3 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030 | 3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1133+1904C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285647 | ||||||
| chr1:47285919
|
G | A | 19 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(16): Show | 19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1133+1632C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285919 | ||||||
| chr1:47286143
|
A | G | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.1133+1408T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286143 | ||||||
| chr1:47286277
|
C | T | 2 | a0001c0003t0001g0083a0001c0003t0001g0184 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1133+1274G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286277 | ||||||
| chr1:47286278
|
G | A | 28 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(25): Show | 28 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1133+1273C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286278 | ||||||
| chr1:47286292
|
C | T | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1133+1259G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286292 | ||||||
| chr1:47286323
|
C | T | 37 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(34): Show | 37 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1133+1228G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286323 | ||||||
| chr1:47286396
|
G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1133+1155C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286396 | ||||||
| chr1:47286407
|
C | T | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+1144G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286407 | ||||||
| chr1:47286428
|
G | A | 44 | a0003c0004t0001g0004a0003c0004t0001g0031a0003c0004t0001g0332others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1133+1123C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286428 | ||||||
| chr1:47286447
|
G | A | 1 | a0001c0003t0001g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1133+1104C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286447 | ||||||
| chr1:47286572
|
G | A | 1 | a0002c0001t0002g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1133+979C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286572 | ||||||
| chr1:47286588
|
G | A | 35 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(32): Show | 35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1133+963C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286588 | ||||||
| chr1:47286648
|
T | C | 1 | a0002c0001t0002g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1133+903A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286648 | ||||||
| chr1:47286651
|
G | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+900C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286651 | ||||||
| chr1:47286660
|
C | T | 3 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016 | 3 | HG01069.hp2 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1133+891G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286660 | ||||||
| chr1:47286794
|
G | A | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1133+757C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286794 | ||||||
| chr1:47286829
|
C | T | 2 | a0001c0002t0001g0077a0001c0002t0001g0078 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1133+722G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286829 | ||||||
| chr1:47286835
|
C | T | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.1133+716G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286835 | ||||||
| chr1:47286924
|
T | A | 2 | a0001c0002t0004g0211a0011c0018t0008g0212 | 2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1133+627A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286924 | ||||||
| chr1:47286928
|
G | C | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1133+623C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286928 | ||||||
| chr1:47286963
|
T | C | 4 | a0002c0001t0002g0259a0002c0001t0002g0265a0002c0001t0002g0266others(1): Show | 4 | HG00738.hp1 HG01433.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133+588A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286963 | ||||||
| chr1:47286964
|
C | T | 1 | a0002c0001t0002g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1133+587G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286964 | ||||||
| chr1:47287060
|
A | C | 59 | a0001c0003t0006g0026a0001c0003t0006g0027a0003c0004t0001g0004others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1133+491T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287060 | ||||||
| chr1:47287085
|
G | A | 56 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(53): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1133+466C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287085 | ||||||
| chr1:47287275
|
T | G | 1 | a0002c0001t0002g0304 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1133+276A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287275 | ||||||
| chr1:47287293
|
T | C | 1 | a0015c0016t0001g0368 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1133+258A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287293 | ||||||
| chr1:47287324
|
T | C | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.1133+227A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287324 | ||||||
| chr1:47287379
|
A | C | 1 | a0002c0001t0002g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1133+172T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287379 | ||||||
| chr1:47287407
|
G | C | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+144C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287407 | ||||||
| chr1:47287489
|
C | T | 3 | a0001c0002t0001g0149a0001c0002t0001g0150a0001c0002t0001g0208 | 3 | NA18959.hp1 NA18989.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1133+62G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287489 | ||||||
| chr1:47287733
|
G | A | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1024-73C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287733 | ||||||
| chr1:47287752
|
T | A | 19 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(16): Show | 19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1024-92A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287752 | ||||||
| chr1:47287885
|
C | T | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-225G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287885 | ||||||
| chr1:47287993
|
A | G | 1 | a0001c0003t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1024-333T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287993 | ||||||
| chr1:47287997
|
T | C | 6 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-337A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287997 | ||||||
| chr1:47288074
|
A | T | 1 | a0001c0002t0003g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1024-414T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288074 | ||||||
| chr1:47288104
|
G | A | 5 | a0001c0002t0001g0148a0001c0002t0001g0162a0001c0002t0001g0163others(2): Show | 5 | HG00408.hp2 HG02056.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-444C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288104 | ||||||
| chr1:47288152
|
G | C | 34 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(31): Show | 34 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1024-492C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288152 | ||||||
| chr1:47288278
|
C | A | 26 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(23): Show | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1024-618G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288278 | ||||||
| chr1:47288312
|
T | C | 1 | a0002c0001t0002g0315 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1024-652A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288312 | ||||||
| chr1:47288405
|
T | G | 1 | a0002c0001t0002g0040 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1024-745A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288405 | ||||||
| chr1:47288423
|
A | G | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-763T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288423 | ||||||
| chr1:47288548
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1023+887G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288548 | ||||||
| chr1:47288572
|
G | A | 1 | a0001c0003t0001g0226 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1023+863C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288572 | ||||||
| chr1:47288597
|
T | A | 1 | a0001c0002t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1023+838A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288597 | ||||||
| chr1:47288792
|
A | C | 1 | a0003c0004t0001g0373 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1023+643T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288792 | ||||||
| chr1:47288892
|
C | CA | 8 | a0002c0001t0002g0036a0002c0001t0002g0043a0002c0001t0002g0246others(5): Show | 8 | HG01433.hp1 HG01978.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+542dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288892 | ||||||
| chr1:47288892
|
CA | C | 81 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(78): Show | 83 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1023+542delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288892 | ||||||
| chr1:47288892
|
CAA | C | 144 | a0001c0002t0001g0088a0001c0002t0001g0147a0001c0002t0001g0148others(141): Show | 146 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.1023+541_1023+542d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288892 | ||||||
| chr1:47288912
|
A | G | 1 | a0001c0002t0001g0147 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1023+523T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288912 | ||||||
| chr1:47288913
|
A | T | 253 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(250): Show | 257 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.1023+522T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288913 | ||||||
| chr1:47288927
|
T | C | 7 | a0002c0001t0002g0052a0002c0001t0002g0060a0002c0001t0002g0383others(4): Show | 7 | HG00280.hp2 HG02132.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+508A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288927 | ||||||
| chr1:47288957
|
G | T | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1023+478C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288957 | ||||||
| chr1:47288958
|
A | C | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1023+477T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288958 | ||||||
| chr1:47289028
|
C | G | 32 | a0002c0001t0002g0033a0002c0001t0002g0034a0002c0001t0002g0035others(29): Show | 32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1023+407G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289028 | ||||||
| chr1:47289049
|
G | A | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1023+386C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289049 | ||||||
| chr1:47289061
|
C | CAA | 72 | a0001c0002t0001g0070a0001c0002t0001g0187a0001c0002t0001g0188others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.1023+372_1023+373d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289061 | ||||||
| chr1:47289061
|
C | CAAA | 19 | a0002c0001t0002g0032a0002c0001t0002g0237a0002c0001t0002g0238others(16): Show | 19 | HG00621.hp2 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1023+371_1023+373d others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289061 | ||||||
| chr1:47289061
|
CA | C | 101 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(98): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1023+373delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289061 | ||||||
| chr1:47289073
|
A | AC | 4 | a0001c0002t0001g0073a0001c0002t0001g0095a0001c0002t0001g0181others(1): Show | 4 | HG02056.hp2 NA18985.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+361_1023+362i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289073 | ||||||
| chr1:47289073
|
A | C | 140 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(137): Show | 142 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1023+362T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289073 | ||||||
| chr1:47289078
|
A | C | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1023+357T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289078 | ||||||
| chr1:47289080
|
A | AC | 12 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(9): Show | 13 | HG00639.hp2 HG01891.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1023+354_1023+355i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289080 | ||||||
| chr1:47289080
|
A | C | 226 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(223): Show | 229 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.1023+355T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289080 | ||||||
| chr1:47289318
|
TAAAC | T | 34 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(31): Show | 34 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1023+113_1023+116d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289318 | ||||||
| chr1:47289362
|
G | A | 1 | a0002c0001t0002g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1023+73C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289362 | ||||||
| chr1:47289644
|
T | C | 32 | a0002c0001t0002g0033a0002c0001t0002g0034a0002c0001t0002g0035others(29): Show | 32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.873-59A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289644 | ||||||
| chr1:47289653
|
G | A | 3 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020 | 3 | HG02257.hp1 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.873-68C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289653 | ||||||
| chr1:47289749
|
C | T | 1 | a0002c0001t0002g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.873-164G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289749 | ||||||
| chr1:47289787
|
T | C | 1 | a0001c0003t0001g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.873-202A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289787 | ||||||
| chr1:47289803
|
C | T | 1 | a0003c0004t0001g0382 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.873-218G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289803 | ||||||
| chr1:47289916
|
C | T | 2 | a0002c0001t0002g0037a0002c0001t0002g0045 | 2 | HG02155.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.873-331G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289916 | ||||||
| chr1:47289938
|
C | CA | 9 | a0002c0001t0002g0043a0002c0001t0002g0247a0002c0001t0002g0298others(6): Show | 9 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.873-354dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289938 | ||||||
| chr1:47289938
|
CA | C | 169 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(166): Show | 172 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-354delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289938 | ||||||
| chr1:47289938
|
CAA | C | 66 | a0001c0002t0001g0146a0001c0002t0003g0007a0001c0002t0003g0008others(63): Show | 67 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.873-355_873-354del others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289938 | ||||||
| chr1:47289955
|
A | C | 24 | a0001c0002t0001g0070a0001c0002t0001g0187a0001c0002t0001g0188others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.873-370T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289955 | ||||||
| chr1:47289995
|
G | A | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.873-410C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289995 | ||||||
| chr1:47290068
|
A | G | 26 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(23): Show | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.873-483T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290068 | ||||||
| chr1:47290161
|
G | C | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.873-576C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290161 | ||||||
| chr1:47290378
|
T | G | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.873-793A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290378 | ||||||
| chr1:47290380
|
T | G | 253 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(250): Show | 257 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.873-795A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290380 | ||||||
| chr1:47290576
|
A | ACCTGTAG others(10): Show |
1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.873-1008_873-992du others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290576 | ||||||
| chr1:47290596
|
GGGAGGCT others(651): Show |
G | 1 | a0004c0005t0002g0063 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.873-1669_873-1012d others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290596 | ||||||
| chr1:47290604
|
G | A | 1 | a0002c0001t0002g0057 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.873-1019C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290604 | ||||||
| chr1:47290654
|
G | A | 1 | a0002c0001t0002g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.873-1069C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290654 | ||||||
| chr1:47290791
|
T | G | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.873-1206A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290791 | ||||||
| chr1:47291083
|
G | A | 1 | a0002c0001t0002g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.873-1498C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291083 | ||||||
| chr1:47291222
|
A | G | 259 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(256): Show | 263 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.873-1637T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291222 | ||||||
| chr1:47291246
|
A | G | 50 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(47): Show | 51 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.873-1661T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291246 | ||||||
| chr1:47291263
|
A | G | 1 | a0002c0001t0002g0044 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.873-1678T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291263 | ||||||
| chr1:47291276
|
G | A | 1 | a0002c0001t0015g0388 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.873-1691C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291276 | ||||||
| chr1:47291412
|
TTAAA | T | 10 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(7): Show | 10 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-1831_873-1828d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291412 | ||||||
| chr1:47291537
|
A | G | 1 | a0001c0002t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.872+1921T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291537 | ||||||
| chr1:47291579
|
T | A | 4 | a0001c0002t0001g0067a0001c0002t0001g0167a0001c0002t0001g0168others(1): Show | 4 | NA18948.hp1 NA18951.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1879A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291579 | ||||||
| chr1:47291579
|
T | TA | 4 | a0003c0004t0001g0375a0003c0004t0001g0376a0003c0004t0001g0377others(1): Show | 4 | HG02896.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1878_872+1879i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291579 | ||||||
| chr1:47291679
|
C | T | 2 | a0002c0001t0002g0239a0002c0001t0002g0258 | 2 | NA18949.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.872+1779G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291679 | ||||||
| chr1:47291812
|
C | T | 31 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(28): Show | 31 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.872+1646G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291812 | ||||||
| chr1:47291899
|
T | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1559A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291899 | ||||||
| chr1:47291905
|
T | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1553A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291905 | ||||||
| chr1:47291906
|
G | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1552C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291906 | ||||||
| chr1:47291907
|
G | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1551C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291907 | ||||||
| chr1:47291908
|
A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1550T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291908 | ||||||
| chr1:47291923
|
T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1535A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291923 | ||||||
| chr1:47291933
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1525G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291933 | ||||||
| chr1:47291934
|
T | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1524A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291934 | ||||||
| chr1:47291935
|
G | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1523C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291935 | ||||||
| chr1:47291939
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1519G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291939 | ||||||
| chr1:47291944
|
A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1514T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291944 | ||||||
| chr1:47291947
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1511G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291947 | ||||||
| chr1:47291955
|
C | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1503G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291955 | ||||||
| chr1:47291956
|
A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1502T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291956 | ||||||
| chr1:47291957
|
A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1501T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291957 | ||||||
| chr1:47291959
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1499G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291959 | ||||||
| chr1:47291960
|
G | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1498C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291960 | ||||||
| chr1:47291963
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1495G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291963 | ||||||
| chr1:47292029
|
G | GT | 19 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(16): Show | 19 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.872+1428dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292029 | ||||||
| chr1:47292093
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1365G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292093 | ||||||
| chr1:47292095
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1363G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292095 | ||||||
| chr1:47292096
|
A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1362T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292096 | ||||||
| chr1:47292099
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1359G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292099 | ||||||
| chr1:47292100
|
G | T | 1 | a0001c0002t0001g0076 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.872+1358C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292100 | ||||||
| chr1:47292103
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1355G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292103 | ||||||
| chr1:47292104
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1354G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292104 | ||||||
| chr1:47292105
|
T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1353A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292105 | ||||||
| chr1:47292106
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1352G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292106 | ||||||
| chr1:47292107
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1351G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292107 | ||||||
| chr1:47292110
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1348G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292110 | ||||||
| chr1:47292111
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1347G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292111 | ||||||
| chr1:47292113
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1345G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292113 | ||||||
| chr1:47292114
|
A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1344T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292114 | ||||||
| chr1:47292116
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1342G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292116 | ||||||
| chr1:47292117
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1341G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292117 | ||||||
| chr1:47292119
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1339G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292119 | ||||||
| chr1:47292120
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1338G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292120 | ||||||
| chr1:47292121
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1337G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292121 | ||||||
| chr1:47292122
|
A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1336T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292122 | ||||||
| chr1:47292123
|
A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1335T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292123 | ||||||
| chr1:47292129
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1329G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292129 | ||||||
| chr1:47292130
|
A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1328T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292130 | ||||||
| chr1:47292136
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1322G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292136 | ||||||
| chr1:47292138
|
G | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1320C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292138 | ||||||
| chr1:47292149
|
C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1309G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292149 | ||||||
| chr1:47292150
|
A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1308T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292150 | ||||||
| chr1:47292152
|
A | G | 354 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(351): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.872+1306T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292152 | ||||||
| chr1:47292152
|
A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1306T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292152 | ||||||
| chr1:47292164
|
C | G | 5 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(2): Show | 5 | HG00642.hp1 HG02572.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1294G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292164 | ||||||
| chr1:47292194
|
T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1264A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292194 | ||||||
| chr1:47292200
|
C | CAGGGGGG others(3): Show |
1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1257_872+1258i others(12): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292200 | ||||||
| chr1:47292201
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1257G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292201 | ||||||
| chr1:47292202
|
A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1256T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292202 | ||||||
| chr1:47292204
|
T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1254A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292204 | ||||||
| chr1:47292205
|
A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1253T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292205 | ||||||
| chr1:47292206
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1252G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292206 | ||||||
| chr1:47292207
|
T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1251A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292207 | ||||||
| chr1:47292209
|
T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1249A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292209 | ||||||
| chr1:47292211
|
A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1247T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292211 | ||||||
| chr1:47292212
|
A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1246T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292212 | ||||||
| chr1:47292213
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1245G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292213 | ||||||
| chr1:47292214
|
A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1244T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292214 | ||||||
| chr1:47292217
|
A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1241T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292217 | ||||||
| chr1:47292299
|
G | A | 30 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(27): Show | 30 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.872+1159C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292299 | ||||||
| chr1:47292311
|
A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1147T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292311 | ||||||
| chr1:47292320
|
A | AATTGAGT others(6): Show |
1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1137_872+1138i others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292320 | ||||||
| chr1:47292347
|
A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1111T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292347 | ||||||
| chr1:47292426
|
T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1032A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292426 | ||||||
| chr1:47292442
|
C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1016G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292442 | ||||||
| chr1:47292486
|
A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+972T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292486 | ||||||
| chr1:47292512
|
CAG | C | 17 | a0001c0002t0001g0068a0001c0002t0001g0069a0001c0002t0001g0071others(14): Show | 17 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.872+944_872+945del others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292512 | ||||||
| chr1:47292513
|
A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+945T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292513 | ||||||
| chr1:47292519
|
T | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+939A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292519 | ||||||
| chr1:47292526
|
A | T | 387 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(384): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.872+932T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292526 | ||||||
| chr1:47292542
|
A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+916T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292542 | ||||||
| chr1:47292558
|
C | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+900G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292558 | ||||||
| chr1:47292571
|
GAGGTAAT others(36): Show |
G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+844_872+886del others(43): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292571 | ||||||
| chr1:47292589
|
G | A | 1 | a0003c0004t0001g0359 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.872+869C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292589 | ||||||
| chr1:47292614
|
C | A | 1 | a0001c0002t0001g0183 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.872+844G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292614 | ||||||
| chr1:47292709
|
G | A | 1 | a0001c0002t0004g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.872+749C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292709 | ||||||
| chr1:47293206
|
T | C | 4 | a0001c0002t0001g0176a0001c0002t0001g0178a0001c0002t0001g0179others(1): Show | 4 | HG02602.hp1 HG03654.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+252A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47293206 | ||||||
| chr1:47293276
|
C | A | 1 | a0002c0001t0002g0383 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.872+182G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47293276 | ||||||
| chr1:47293560
|
A | T | 1 | a0002c0001t0002g0238 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.786-16T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47293560 | ||||||
| chr1:47294224
|
A | G | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.786-680T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294224 | ||||||
| chr1:47294347
|
C | A | 2 | a0001c0003t0001g0135a0001c0003t0001g0136 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.786-803G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294347 | ||||||
| chr1:47294387
|
C | T | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.786-843G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294387 | ||||||
| chr1:47294554
|
C | T | 11 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(8): Show | 11 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.786-1010G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294554 | ||||||
| chr1:47294591
|
G | A | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.786-1047C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294591 | ||||||
| chr1:47294699
|
T | A | 56 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(53): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.785+1066A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294699 | ||||||
| chr1:47294864
|
G | A | 5 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+901C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294864 | ||||||
| chr1:47294929
|
A | AT | 7 | a0001c0002t0004g0228a0001c0002t0004g0229a0001c0002t0004g0230others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.785+835dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294929 | ||||||
| chr1:47294954
|
T | C | 1 | a0001c0002t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.785+811A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294954 | ||||||
| chr1:47294986
|
A | G | 3 | a0002c0001t0002g0253a0002c0001t0002g0254a0002c0001t0011g0306 | 3 | HG00099.hp2 HG00140.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.785+779T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294986 | ||||||
| chr1:47295112
|
G | A | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.785+653C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295112 | ||||||
| chr1:47295116
|
T | C | 1 | a0001c0002t0001g0180 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.785+649A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295116 | ||||||
| chr1:47295120
|
A | G | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.785+645T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295120 | ||||||
| chr1:47295142
|
T | TGAACTCC others(7): Show |
1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.785+609_785+622dup others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295142 | ||||||
| chr1:47295143
|
G | C | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.785+622C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295143 | ||||||
| chr1:47295230
|
C | A | 3 | a0002c0001t0002g0248a0002c0001t0002g0300a0002c0001t0002g0320 | 3 | HG02083.hp1 NA18995.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.785+535G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295230 | ||||||
| chr1:47295297
|
T | C | 147 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.785+468A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295297 | ||||||
| chr1:47295984
|
CAG | C | 4 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(1): Show | 4 | HG00323.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.702-138_702-137del others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47295984 | ||||||
| chr1:47296050
|
C | A | 2 | a0001c0002t0003g0012a0001c0002t0003g0013 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.702-202G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296050 | ||||||
| chr1:47296137
|
C | T | 1 | a0002c0001t0002g0043 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.702-289G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296137 | ||||||
| chr1:47296219
|
A | G | 256 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(253): Show | 260 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.702-371T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296219 | ||||||
| chr1:47296303
|
T | G | 2 | a0003c0004t0001g0365a0003c0004t0001g0366 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.702-455A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296303 | ||||||
| chr1:47296421
|
A | T | 7 | a0001c0003t0001g0218a0001c0003t0001g0219a0001c0003t0001g0220others(4): Show | 7 | HG00639.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.702-573T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296421 | ||||||
| chr1:47296703
|
G | A | 1 | a0001c0003t0001g0137 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.702-855C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296703 | ||||||
| chr1:47296836
|
G | A | 1 | a0003c0004t0001g0381 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.702-988C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296836 | ||||||
| chr1:47296922
|
G | T | 1 | a0002c0001t0002g0060 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.702-1074C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296922 | ||||||
| chr1:47297219
|
G | A | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.702-1371C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297219 | ||||||
| chr1:47297231
|
A | C | 5 | a0002c0001t0013g0062a0004c0005t0002g0063a0004c0005t0002g0064others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.702-1383T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297231 | ||||||
| chr1:47297304
|
C | G | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.702-1456G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297304 | ||||||
| chr1:47297343
|
C | CA | 156 | a0002c0001t0002g0032a0002c0001t0002g0042a0002c0001t0002g0056others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.702-1496dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297343 | ||||||
| chr1:47297343
|
CA | C | 6 | a0001c0003t0001g0080a0001c0003t0001g0081a0001c0003t0001g0082others(3): Show | 6 | HG01109.hp1 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.702-1496delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297343 | ||||||
| chr1:47297480
|
A | T | 13 | a0001c0003t0001g0001a0001c0003t0001g0079a0001c0003t0001g0100others(10): Show | 14 | HG00621.hp1 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.702-1632T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297480 | ||||||
| chr1:47297535
|
C | T | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.702-1687G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297535 | ||||||
| chr1:47297602
|
G | C | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.702-1754C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297602 | ||||||
| chr1:47297661
|
T | C | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.702-1813A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297661 | ||||||
| chr1:47297829
|
A | G | 1 | a0001c0002t0001g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.702-1981T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297829 | ||||||
| chr1:47297922
|
G | A | 1 | a0001c0003t0001g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.701+1983C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297922 | ||||||
| chr1:47297985
|
G | A | 4 | a0004c0005t0002g0063a0004c0005t0002g0064a0004c0005t0002g0065others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+1920C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297985 | ||||||
| chr1:47297986
|
AAGTACTT others(1): Show |
A | 3 | a0001c0002t0003g0014a0001c0002t0003g0015a0001c0002t0003g0016 | 3 | HG01069.hp2 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.701+1911_701+1918d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297986 | ||||||
| chr1:47298027
|
T | C | 2 | a0001c0002t0004g0211a0011c0018t0008g0212 | 2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.701+1878A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298027 | ||||||
| chr1:47298041
|
C | T | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.701+1864G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298041 | ||||||
| chr1:47298299
|
T | C | 2 | a0001c0002t0001g0002a0001c0002t0001g0094 | 3 | NA18950.hp1 NA19010.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.701+1606A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298299 | ||||||
| chr1:47298471
|
C | T | 147 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.701+1434G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298471 | ||||||
| chr1:47298626
|
G | GA | 7 | a0001c0002t0001g0073a0001c0002t0003g0325a0001c0002t0003g0326others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.701+1278dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298626 | ||||||
| chr1:47298636
|
A | G | 1 | a0001c0002t0001g0188 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.701+1269T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298636 | ||||||
| chr1:47298736
|
G | GT | 15 | a0001c0003t0001g0001a0001c0003t0001g0079a0001c0003t0001g0100others(12): Show | 16 | HG00621.hp1 HG01515.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.701+1168dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298736 | ||||||
| chr1:47298783
|
G | A | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.701+1122C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298783 | ||||||
| chr1:47298815
|
C | T | 11 | a0001c0003t0001g0003a0001c0003t0001g0217a0001c0003t0001g0218others(8): Show | 12 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.701+1090G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298815 | ||||||
| chr1:47298978
|
T | A | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | NA18951.hp1 NA18960.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+927A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298978 | ||||||
| chr1:47299033
|
C | CT | 245 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(242): Show | 249 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.701+871dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299033 | ||||||
| chr1:47299116
|
G | A | 8 | a0002c0001t0002g0235a0002c0001t0002g0249a0002c0001t0002g0302others(5): Show | 8 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+789C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299116 | ||||||
| chr1:47299134
|
A | G | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.701+771T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299134 | ||||||
| chr1:47299305
|
C | A | 1 | a0002c0001t0002g0305 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.701+600G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299305 | ||||||
| chr1:47299396
|
T | G | 1 | a0001c0003t0001g0143 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.701+509A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299396 | ||||||
| chr1:47299400
|
C | CT | 256 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(253): Show | 260 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.701+504dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299400 | ||||||
| chr1:47299455
|
C | T | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.701+450G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299455 | ||||||
| chr1:47299466
|
C | T | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.701+439G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299466 | ||||||
| chr1:47299509
|
C | T | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.701+396G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299509 | ||||||
| chr1:47299550
|
G | A | 1 | a0002c0001t0002g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.701+355C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299550 | ||||||
| chr1:47299717
|
T | C | 77 | a0001c0003t0001g0001a0001c0003t0001g0074a0001c0003t0001g0075others(74): Show | 78 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.701+188A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299717 | ||||||
| chr1:47299758
|
C | A | 4 | a0001c0002t0003g0017a0001c0002t0003g0018a0001c0002t0003g0019others(1): Show | 4 | HG02257.hp1 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+147G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299758 | ||||||
| chr1:47299818
|
T | C | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.701+87A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299818 | ||||||
| chr1:47300383
|
C | A | 4 | a0003c0004t0001g0369a0003c0004t0001g0373a0003c0004t0001g0374others(1): Show | 4 | HG00642.hp2 HG00735.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-231G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300383 | ||||||
| chr1:47300440
|
T | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-288A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300440 | ||||||
| chr1:47300473
|
T | TTC | 240 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(237): Show | 243 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.454-322_454-321ins others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300473 | ||||||
| chr1:47300475
|
T | C | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.454-323A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300475 | ||||||
| chr1:47300543
|
A | T | 3 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030 | 3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.454-391T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300543 | ||||||
| chr1:47300562
|
G | A | 56 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(53): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.454-410C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300562 | ||||||
| chr1:47300752
|
G | A | 1 | a0002c0001t0002g0250 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.454-600C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300752 | ||||||
| chr1:47300932
|
A | G | 355 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(352): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.453+629T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300932 | ||||||
| chr1:47300975
|
C | T | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.453+586G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300975 | ||||||
| chr1:47301171
|
G | A | 1 | a0002c0001t0002g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.453+390C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301171 | ||||||
| chr1:47301198
|
T | C | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.453+363A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301198 | ||||||
| chr1:47301271
|
T | C | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.453+290A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301271 | ||||||
| chr1:47301469
|
C | A | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.453+92G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301469 | ||||||
| chr1:47301543
|
G | A | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.453+18C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301543 | ||||||
| chr1:47301929
|
G | A | 1 | a0001c0003t0001g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.266-181C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 4/16 | chr1 | 47301929 | ||||||
| chr1:47302182
|
A | G | 1 | a0002c0001t0002g0237 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.265+52T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 4/16 | chr1 | 47302182 | ||||||
| chr1:47302401
|
C | A | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.153-55G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302401 | ||||||
| chr1:47302498
|
C | G | 1 | a0003c0004t0001g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.153-152G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302498 | ||||||
| chr1:47302512
|
G | A | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-166C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302512 | ||||||
| chr1:47302541
|
A | C | 1 | a0002c0001t0002g0037 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.153-195T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302541 | ||||||
| chr1:47302563
|
A | G | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153-217T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302563 | ||||||
| chr1:47302611
|
A | G | 2 | a0001c0002t0004g0211a0011c0018t0008g0212 | 2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.153-265T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302611 | ||||||
| chr1:47302729
|
G | T | 1 | a0001c0003t0006g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153-383C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302729 | ||||||
| chr1:47302894
|
G | A | 1 | a0001c0002t0001g0183 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.153-548C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302894 | ||||||
| chr1:47303023
|
G | T | 23 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(20): Show | 23 | HG01069.hp2 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.153-677C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303023 | ||||||
| chr1:47303071
|
T | C | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.153-725A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303071 | ||||||
| chr1:47303248
|
T | C | 16 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(13): Show | 16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.153-902A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303248 | ||||||
| chr1:47303256
|
C | T | 11 | a0001c0003t0001g0003a0001c0003t0001g0217a0001c0003t0001g0218others(8): Show | 12 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-910G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303256 | ||||||
| chr1:47303755
|
T | C | 1 | a0002c0001t0002g0305 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.152+1134A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303755 | ||||||
| chr1:47303805
|
T | C | 66 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(63): Show | 67 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.152+1084A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303805 | ||||||
| chr1:47303928
|
T | C | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+961A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303928 | ||||||
| chr1:47304149
|
G | GT | 9 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(6): Show | 9 | HG01167.hp2 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+739dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304149 | ||||||
| chr1:47304351
|
A | T | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.152+538T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304351 | ||||||
| chr1:47304454
|
T | C | 1 | a0001c0002t0003g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.152+435A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304454 | ||||||
| chr1:47304591
|
G | A | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.152+298C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304591 | ||||||
| chr1:47304724
|
G | A | 3 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030 | 3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.152+165C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304724 | ||||||
| chr1:47304741
|
G | C | 1 | a0001c0003t0006g0026 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.152+148C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304741 | ||||||
| chr1:47304744
|
G | A | 6 | a0001c0002t0004g0211a0001c0002t0004g0228a0001c0002t0004g0229others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+145C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304744 | ||||||
| chr1:47304769
|
A | C | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.152+120T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304769 | ||||||
| chr1:47304794
|
T | C | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.152+95A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304794 | ||||||
| chr1:47305114
|
T | A | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.45-118A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305114 | ||||||
| chr1:47305134
|
T | C | 57 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(54): Show | 58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.45-138A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305134 | ||||||
| chr1:47305137
|
T | A | 9 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-141A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305137 | ||||||
| chr1:47305237
|
T | C | 1 | a0001c0003t0001g0185 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.45-241A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305237 | ||||||
| chr1:47305315
|
G | A | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.45-319C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305315 | ||||||
| chr1:47305369
|
C | G | 1 | a0003c0004t0001g0362 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45-373G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305369 | ||||||
| chr1:47305548
|
C | A | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45-552G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305548 | ||||||
| chr1:47305642
|
G | A | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.45-646C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305642 | ||||||
| chr1:47305711
|
C | G | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45-715G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305711 | ||||||
| chr1:47305717
|
C | T | 1 | a0003c0004t0001g0362 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45-721G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305717 | ||||||
| chr1:47305725
|
C | CT | 105 | a0001c0002t0003g0028a0001c0002t0004g0229a0001c0002t0004g0231others(102): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.45-730dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | ||||||
| chr1:47305725
|
C | CTT | 59 | a0002c0001t0002g0033a0002c0001t0002g0037a0002c0001t0002g0039others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45-731_45-730dupAA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | ||||||
| chr1:47305725
|
C | CTTT | 19 | a0003c0004t0001g0022a0003c0004t0001g0024a0003c0004t0001g0333others(16): Show | 19 | HG00735.hp1 HG00738.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-732_45-730dupAA others(1): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | ||||||
| chr1:47305725
|
CT | C | 139 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(136): Show | 142 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.45-730delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | ||||||
| chr1:47305725
|
CTT | C | 18 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(15): Show | 18 | HG01069.hp2 HG02257.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-731_45-730delAA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | ||||||
| chr1:47305725
|
CTTTTTTT others(4): Show |
C | 2 | a0003c0004t0001g0347a0003c0004t0001g0348 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.45-740_45-730delAA others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | ||||||
| chr1:47305819
|
G | A | 4 | a0001c0003t0001g0322a0001c0003t0001g0323a0001c0003t0001g0324others(1): Show | 4 | HG01167.hp2 HG02976.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-823C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305819 | ||||||
| chr1:47305881
|
G | A | 1 | a0002c0001t0002g0057 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.45-885C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305881 | ||||||
| chr1:47305893
|
A | G | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-897T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305893 | ||||||
| chr1:47305921
|
C | T | 1 | a0002c0001t0002g0037 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.45-925G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305921 | ||||||
| chr1:47306010
|
C | T | 2 | a0001c0002t0004g0211a0011c0018t0008g0212 | 2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.45-1014G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306010 | ||||||
| chr1:47306125
|
T | C | 3 | a0001c0002t0001g0070a0001c0002t0001g0187a0001c0002t0001g0188 | 3 | NA18979.hp1 NA18982.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.45-1129A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306125 | ||||||
| chr1:47306190
|
T | C | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.45-1194A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306190 | ||||||
| chr1:47306264
|
CT | C | 132 | a0001c0002t0001g0076a0001c0002t0004g0231a0001c0003t0001g0075others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.45-1269delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306264 | ||||||
| chr1:47306264
|
CTT | C | 246 | a0001c0002t0001g0002a0001c0002t0001g0068a0001c0002t0001g0069others(243): Show | 250 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.45-1270_45-1269del others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306264 | ||||||
| chr1:47306264
|
CTTT | C | 8 | a0001c0002t0001g0067a0001c0002t0003g0021a0001c0002t0003g0330others(5): Show | 8 | HG01515.hp1 HG02055.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.45-1271_45-1269del others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306264 | ||||||
| chr1:47306282
|
T | A | 1 | a0001c0002t0004g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45-1286A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306282 | ||||||
| chr1:47306408
|
C | T | 1 | a0001c0003t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.45-1412G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306408 | ||||||
| chr1:47306416
|
A | G | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.45-1420T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306416 | ||||||
| chr1:47306435
|
G | A | 3 | a0005c0007t0004g0213a0005c0007t0004g0214a0005c0017t0004g0215 | 3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45-1439C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306435 | ||||||
| chr1:47306550
|
G | A | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.45-1554C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306550 | ||||||
| chr1:47306562
|
G | A | 2 | a0002c0001t0002g0033a0002c0001t0002g0058 | 2 | NA18947.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.45-1566C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306562 | ||||||
| chr1:47306794
|
T | C | 1 | a0002c0001t0002g0318 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.45-1798A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306794 | ||||||
| chr1:47306950
|
G | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-1954C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306950 | ||||||
| chr1:47306981
|
A | G | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.45-1985T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306981 | ||||||
| chr1:47307001
|
A | G | 1 | a0001c0003t0001g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.45-2005T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307001 | ||||||
| chr1:47307044
|
C | G | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.45-2048G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307044 | ||||||
| chr1:47307130
|
G | A | 1 | a0014c0014t0001g0191 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.45-2134C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307130 | ||||||
| chr1:47307354
|
C | T | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45-2358G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307354 | ||||||
| chr1:47307514
|
C | T | 1 | a0001c0003t0001g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.45-2518G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307514 | ||||||
| chr1:47307660
|
C | T | 1 | a0002c0001t0002g0236 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.44+2616G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307660 | ||||||
| chr1:47307828
|
G | A | 4 | a0002c0001t0002g0314a0002c0001t0002g0315a0002c0001t0002g0316others(1): Show | 4 | HG01071.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+2448C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307828 | ||||||
| chr1:47307868
|
C | T | 6 | a0003c0004t0001g0354a0003c0004t0001g0355a0003c0004t0001g0356others(3): Show | 6 | HG00597.hp2 HG02109.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+2408G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307868 | ||||||
| chr1:47308039
|
G | A | 2 | a0003c0004t0001g0024a0003c0004t0001g0025 | 2 | HG00642.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.44+2237C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308039 | ||||||
| chr1:47308162
|
C | T | 1 | a0002c0001t0002g0235 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.44+2114G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308162 | ||||||
| chr1:47308356
|
C | T | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.44+1920G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308356 | ||||||
| chr1:47308376
|
C | T | 147 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.44+1900G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308376 | ||||||
| chr1:47308380
|
G | A | 16 | a0001c0003t0001g0003a0001c0003t0001g0216a0001c0003t0001g0217others(13): Show | 17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.44+1896C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308380 | ||||||
| chr1:47308427
|
G | GA | 354 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(351): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.44+1848dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308427 | ||||||
| chr1:47308594
|
G | A | 147 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.44+1682C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308594 | ||||||
| chr1:47308753
|
T | A | 1 | a0001c0003t0001g0192 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.44+1523A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308753 | ||||||
| chr1:47308764
|
A | G | 1 | a0001c0002t0001g0073 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.44+1512T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308764 | ||||||
| chr1:47308902
|
G | A | 1 | a0002c0001t0002g0318 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.44+1374C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308902 | ||||||
| chr1:47308920
|
C | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.44+1356G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308920 | ||||||
| chr1:47309000
|
C | T | 1 | a0003c0004t0001g0332 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.44+1276G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309000 | ||||||
| chr1:47309016
|
C | A | 5 | a0001c0003t0001g0193a0001c0003t0001g0194a0001c0003t0001g0195others(2): Show | 5 | NA18942.hp2 NA18949.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+1260G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309016 | ||||||
| chr1:47309052
|
C | CA | 7 | a0001c0002t0001g0198a0001c0002t0003g0325a0001c0002t0003g0326others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+1223dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309052 | ||||||
| chr1:47309062
|
A | T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.44+1214T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309062 | ||||||
| chr1:47309065
|
A | T | 104 | a0001c0002t0001g0072a0001c0002t0003g0006a0001c0002t0003g0227others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.44+1211T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309065 | ||||||
| chr1:47309067
|
AT | A | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.44+1208delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309067 | ||||||
| chr1:47309068
|
T | A | 4 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(1): Show | 4 | HG02055.hp2 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+1208A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309068 | ||||||
| chr1:47309172
|
G | A | 1 | a0001c0003t0010g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.44+1104C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309172 | ||||||
| chr1:47309233
|
A | G | 2 | a0002c0001t0002g0233a0002c0001t0002g0234 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.44+1043T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309233 | ||||||
| chr1:47309241
|
T | A | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.44+1035A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309241 | ||||||
| chr1:47309350
|
T | C | 3 | a0001c0002t0001g0071a0001c0002t0001g0200a0001c0002t0001g0201 | 3 | NA18971.hp1 NA18995.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.44+926A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309350 | ||||||
| chr1:47309445
|
T | C | 1 | a0001c0002t0001g0202 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.44+831A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309445 | ||||||
| chr1:47309482
|
T | C | 1 | a0011c0018t0008g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44+794A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309482 | ||||||
| chr1:47309505
|
C | T | 44 | a0003c0004t0001g0004a0003c0004t0001g0031a0003c0004t0001g0332others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.44+771G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309505 | ||||||
| chr1:47309655
|
A | G | 1 | a0003c0004t0001g0352 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44+621T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309655 | ||||||
| chr1:47309679
|
G | A | 8 | a0003c0004t0001g0369a0003c0004t0001g0371a0003c0004t0001g0372others(5): Show | 8 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+597C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309679 | ||||||
| chr1:47309818
|
A | G | 7 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0009others(4): Show | 7 | HG02622.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.44+458T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309818 | ||||||
| chr1:47309975
|
G | T | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.44+301C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309975 | ||||||
| chr1:47309980
|
G | A | 1 | a0003c0004t0001g0382 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+296C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309980 | ||||||
| chr1:47310470
|
T | G | 1 | a0001c0002t0001g0203 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-43-108A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47310470 | ||||||
| chr1:47310524
|
T | C | 1 | a0002c0001t0002g0320 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-43-162A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47310524 | ||||||
| chr1:47310673
|
A | C | 56 | a0003c0004t0001g0004a0003c0004t0001g0022a0003c0004t0001g0023others(53): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-43-311T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47310673 | ||||||
| chr1:47310933
|
C | T | 1 | a0002c0001t0002g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-43-571G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47310933 | ||||||
| chr1:47311095
|
C | A | 5 | a0001c0003t0001g0204a0001c0003t0001g0205a0001c0003t0001g0207others(2): Show | 5 | HG01975.hp2 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-733G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311095 | ||||||
| chr1:47311188
|
C | T | 16 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(13): Show | 16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-826G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311188 | ||||||
| chr1:47311200
|
T | C | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-43-838A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311200 | ||||||
| chr1:47311271
|
TTTTCTTT others(5): Show |
T | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-43-921_-43-910del others(12): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311271 | ||||||
| chr1:47311275
|
CT | C | 60 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(57): Show | 61 | HG00099.hp1 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-43-914delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311275 | ||||||
| chr1:47311282
|
T | C | 1 | a0003c0004t0001g0351 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-43-920A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311282 | ||||||
| chr1:47311283
|
C | CT | 11 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43-922dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311283 | ||||||
| chr1:47311283
|
C | CTT | 16 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(13): Show | 16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-923_-43-922dup others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311283 | ||||||
| chr1:47311283
|
C | T | 2 | a0001c0002t0003g0227a0003c0004t0001g0351 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-43-921G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311283 | ||||||
| chr1:47311283
|
CT | C | 10 | a0001c0002t0001g0208a0001c0003t0001g0209a0002c0001t0002g0059others(7): Show | 10 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-922delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311283 | ||||||
| chr1:47311284
|
T | C | 1 | a0003c0004t0001g0349 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-43-922A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311284 | ||||||
| chr1:47311370
|
C | T | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-43-1008G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311370 | ||||||
| chr1:47311602
|
T | G | 5 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-1240A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311602 | ||||||
| chr1:47311646
|
T | A | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.-43-1284A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311646 | ||||||
| chr1:47311654
|
G | A | 1 | a0001c0002t0001g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-43-1292C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311654 | ||||||
| chr1:47311747
|
G | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-1385C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311747 | ||||||
| chr1:47311803
|
T | C | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-43-1441A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311803 | ||||||
| chr1:47311840
|
A | G | 163 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(160): Show | 166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.-43-1478T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311840 | ||||||
| chr1:47311874
|
C | T | 2 | a0001c0003t0006g0026a0001c0003t0006g0027 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-43-1512G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311874 | ||||||
| chr1:47312180
|
GA | G | 3 | a0005c0007t0004g0213a0005c0007t0004g0214a0005c0017t0004g0215 | 3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-43-1819delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312180 | ||||||
| chr1:47312193
|
C | G | 2 | a0005c0007t0004g0213a0005c0007t0004g0214 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-43-1831G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312193 | ||||||
| chr1:47312196
|
A | G | 1 | a0001c0002t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-43-1834T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312196 | ||||||
| chr1:47312212
|
C | T | 44 | a0003c0004t0001g0004a0003c0004t0001g0031a0003c0004t0001g0332others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.-44+1824G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312212 | ||||||
| chr1:47312358
|
C | T | 2 | a0001c0002t0004g0211a0011c0018t0008g0212 | 2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-44+1678G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312358 | ||||||
| chr1:47312403
|
A | C | 1 | a0001c0002t0001g0067 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-44+1633T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312403 | ||||||
| chr1:47312459
|
A | C | 147 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(144): Show | 149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.-44+1577T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312459 | ||||||
| chr1:47312561
|
G | A | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-44+1475C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312561 | ||||||
| chr1:47312562
|
T | G | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-44+1474A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312562 | ||||||
| chr1:47312594
|
G | A | 16 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(13): Show | 16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-44+1442C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312594 | ||||||
| chr1:47312807
|
A | G | 1 | a0002c0001t0002g0033 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-44+1229T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312807 | ||||||
| chr1:47312848
|
T | C | 257 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(254): Show | 261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.-44+1188A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312848 | ||||||
| chr1:47312905
|
C | A | 1 | a0002c0001t0002g0060 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-44+1131G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312905 | ||||||
| chr1:47313161
|
T | C | 93 | a0002c0001t0002g0032a0002c0001t0002g0061a0002c0001t0002g0232others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-44+875A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313161 | ||||||
| chr1:47313239
|
G | C | 4 | a0001c0003t0001g0322a0001c0003t0001g0323a0001c0003t0001g0324others(1): Show | 4 | HG01167.hp2 HG02976.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+797C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313239 | ||||||
| chr1:47313260
|
G | A | 6 | a0001c0002t0003g0325a0001c0002t0003g0326a0001c0002t0003g0327others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+776C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313260 | ||||||
| chr1:47313344
|
AT | A | 354 | a0001c0002t0001g0002a0001c0002t0001g0067a0001c0002t0001g0068others(351): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-44+691delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313344 | ||||||
| chr1:47313430
|
A | AC | 21 | a0003c0004t0001g0004a0003c0004t0001g0031a0003c0004t0001g0332others(18): Show | 22 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-44+605dupG | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313430 | ||||||
| chr1:47313545
|
C | A | 1 | a0001c0003t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-44+491G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313545 | ||||||
| chr1:47313587
|
CCTT | C | 62 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(59): Show | 63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-44+446_-44+448del others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313587 | ||||||
| chr1:47313692
|
C | T | 1 | a0002c0001t0002g0032 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-44+344G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313692 | ||||||
| chr1:47313720
|
G | A | 5 | a0002c0001t0002g0383a0002c0001t0002g0384a0002c0001t0002g0385others(2): Show | 5 | HG02132.hp2 NA18945.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+316C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313720 | ||||||
| chr1:47313750
|
G | T | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+286C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313750 | ||||||
| chr1:47313784
|
A | C | 1 | a0003c0004t0001g0031 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-44+252T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313784 | ||||||
| chr1:47313951
|
A | C | 5 | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0030others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+85T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313951 | ||||||
| chr1:47314012
|
C | T | 4 | a0003c0004t0001g0022a0003c0004t0001g0023a0003c0004t0001g0024others(1): Show | 4 | HG00642.hp1 HG02572.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+24G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47314012 | ||||||
| chr1:47314021
|
C | T | 16 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0008others(13): Show | 16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-44+15G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47314021 |