| geneid | 166824 |
|---|---|
| ensemblid | ENSG00000169435.14 |
| hgncid | 20796 |
| symbol | RASSF6 |
| name | Ras association domain family member 6 |
| refseq_nuc | NM_177532.5 |
| refseq_prot | NP_803876.1 |
| ensembl_nuc | ENST00000307439.10 |
| ensembl_prot | ENSP00000303877.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 73571550 |
| end | 73620436 |
| strand | - |
| ver | v1.2 |
| region | chr4:73571550-73620436 |
| region5000 | chr4:73566550-73625436 |
| regionname0 | RASSF6_chr4_73571550_73620436 |
| regionname5000 | RASSF6_chr4_73566550_73625436 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 337 | 227 | 50 | 29 | 115 | 10 | 22 | 85 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002 | 0/1 | 337 | 102 | 26 | 36 | 26 | 3 | 10 | 19 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0003 | 0/0 | 337 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0004 | 0/0 | 337 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0005 | 0/0 | 337 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0006 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1014 | 224 | 48 | 29 | 114 | 10 | 22 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0002 | 0/1 | 1014 | 99 | 25 | 36 | 26 | 3 | 8 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0003 | 0/0 | 1014 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0004 | 0/0 | 1014 | 3 | 1 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0005 | 0/0 | 1014 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0006 | 0/0 | 1014 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0007 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0008 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0009 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| c0010 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4869 | 157 | 27 | 24 | 82 | 6 | 18 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0002 | 0/0 | 4869 | 66 | 6 | 30 | 22 | 5 | 3 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0003 | 0/0 | 4869 | 36 | 6 | 2 | 23 | 2 | 3 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0004 | 0/0 | 4869 | 20 | 17 | 3 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0005 | 0/0 | 4869 | 13 | 5 | 0 | 3 | 0 | 5 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0006 | 0/0 | 4869 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0007 | 0/0 | 4869 | 3 | 1 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0008 | 0/0 | 4869 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0009 | 0/0 | 4869 | 3 | 0 | 1 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0010 | 0/0 | 4869 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0011 | 0/0 | 4869 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0012 | 0/0 | 4869 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0013 | 0/0 | 4869 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0014 | 0/0 | 4869 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0015 | 0/0 | 4872 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0016 | 0/0 | 4869 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0017 | 0/0 | 4869 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0018 | 0/0 | 4869 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0019 | 0/0 | 4869 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0020 | 0/0 | 4869 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0021 | 0/0 | 4869 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0022 | 0/1 | 4869 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0023 | 0/0 | 4869 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0024 | 0/0 | 4869 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0025 | 0/0 | 4869 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0026 | 0/0 | 4869 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0027 | 0/0 | 4869 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0028 | 0/0 | 4869 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0029 | 0/0 | 4869 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0030 | 0/0 | 4869 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0031 | 0/0 | 4872 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0032 | 0/0 | 4869 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0033 | 1/0 | 4869 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| t0034 | 0/0 | 4869 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| 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 | 6 | 0 | 5 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0002 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0006 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1014 | 224 | 48 | 29 | 114 | 10 | 22 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0007 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0009 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002 | 0/1 | 1014 | 99 | 25 | 36 | 26 | 3 | 8 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0005 | 0/0 | 1014 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0008 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0003c0003 | 0/0 | 1014 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0004c0004 | 0/0 | 1014 | 3 | 1 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0005c0006 | 0/0 | 1014 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0006c0010 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5882 | 153 | 27 | 23 | 79 | 6 | 18 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0002 | 0/0 | 5882 | 7 | 5 | 0 | 0 | 1 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0003 | 0/0 | 5882 | 35 | 6 | 2 | 23 | 2 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0004 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0007 | 0/0 | 5882 | 3 | 1 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0008 | 0/0 | 5882 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0011 | 0/0 | 5882 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0012 | 0/0 | 5882 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0015 | 0/0 | 5885 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0016 | 0/0 | 5882 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0017 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0018 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0019 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0020 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0021 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0024 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0025 | 0/0 | 5882 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0026 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0028 | 0/0 | 5882 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0029 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0030 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0031 | 0/0 | 5885 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0032 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0001t0033 | 1/0 | 5882 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0007t0014 | 0/0 | 5882 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0001c0009t0001 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0001 | 0/0 | 5882 | 2 | 0 | 1 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0002 | 0/0 | 5882 | 56 | 0 | 29 | 22 | 3 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0003 | 0/0 | 5882 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0004 | 0/0 | 5882 | 18 | 15 | 3 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0005 | 0/0 | 5882 | 10 | 2 | 0 | 3 | 0 | 5 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0006 | 0/0 | 5882 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0009 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0010 | 0/0 | 5882 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0022 | 0/1 | 5882 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0023 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0027 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0002t0034 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0005t0009 | 0/0 | 5882 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0002c0008t0004 | 0/0 | 5882 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0003c0003t0005 | 0/0 | 5882 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0004c0004t0002 | 0/0 | 5882 | 3 | 1 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0005c0006t0013 | 0/0 | 5882 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| a0006c0010t0001 | 0/0 | 5882 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | copy fasta | chr4 | 73566550 | 73625436 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0007g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0011g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0012g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0015g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0016g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0016g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0017g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0018g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0019g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0020g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0021g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0024g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0025g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0026g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0028g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0029g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0030g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0031g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0032g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0001t0033g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0007t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0007t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0001c0009t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0001 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0009g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0022g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0023g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0027g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0002t0034g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0005t0009g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0005t0009g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0002c0008t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0003c0003t0005g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0004c0004t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0004c0004t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0005c0006t0013g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0005c0006t0013g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| a0006c0010t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0181 | EUR | GBR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00140 | hp2 | a0004 | c0004 | t0002 | g0016 | EUR | GBR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | FIN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0255 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00621 | hp1 | a0001 | c0001 | t0030 | g0134 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00639 | hp2 | a0001 | c0001 | t0017 | g0178 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01069 | hp2 | a0002 | c0002 | t0034 | g0274 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01070 | hp1 | a0005 | c0006 | t0013 | g0067 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0021 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0021 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01081 | hp1 | a0005 | c0006 | t0013 | g0068 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01106 | hp2 | a0002 | c0002 | t0023 | g0099 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0004 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01167 | hp2 | a0002 | c0002 | t0004 | g0059 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01243 | hp2 | a0002 | c0002 | t0004 | g0065 | AMR | PUR | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0093 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0199 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0177 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0026 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0168 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01943 | hp2 | a0004 | c0004 | t0002 | g0016 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0082 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02004 | hp2 | a0001 | c0001 | t0019 | g0124 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02027 | hp1 | a0002 | c0002 | t0005 | g0022 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02056 | hp2 | a0002 | c0002 | t0005 | g0022 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | KHV | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02145 | hp1 | a0002 | c0002 | t0006 | g0046 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02148 | hp2 | a0002 | c0002 | t0009 | g0078 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | CDX | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | CDX | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02258 | hp1 | a0002 | c0002 | t0004 | g0015 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02280 | hp2 | a0002 | c0002 | t0004 | g0044 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02615 | hp1 | a0002 | c0002 | t0004 | g0060 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02622 | hp1 | a0002 | c0002 | t0004 | g0004 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02622 | hp2 | a0002 | c0002 | t0005 | g0116 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02630 | hp2 | a0002 | c0002 | t0004 | g0049 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02647 | hp1 | a0001 | c0001 | t0024 | g0224 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02647 | hp2 | a0003 | c0003 | t0005 | g0009 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0204 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0069 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02738 | hp1 | a0002 | c0002 | t0005 | g0119 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02895 | hp1 | a0001 | c0001 | t0015 | g0158 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02895 | hp2 | a0003 | c0003 | t0005 | g0009 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0058 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0157 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0015 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02897 | hp2 | a0003 | c0003 | t0005 | g0009 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02922 | hp2 | a0002 | c0002 | t0004 | g0047 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02976 | hp1 | a0002 | c0002 | t0004 | g0004 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03041 | hp1 | a0002 | c0002 | t0010 | g0123 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03130 | hp2 | a0002 | c0002 | t0006 | g0045 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03139 | hp2 | a0002 | c0002 | t0004 | g0004 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03195 | hp2 | a0001 | c0001 | t0031 | g0156 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03453 | hp1 | a0002 | c0002 | t0004 | g0219 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0206 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0062 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03491 | hp1 | a0002 | c0005 | t0009 | g0083 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03492 | hp2 | a0002 | c0005 | t0009 | g0090 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03516 | hp1 | a0002 | c0002 | t0010 | g0122 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03516 | hp2 | a0002 | c0008 | t0004 | g0048 | AFR | ESN | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0064 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03540 | hp2 | a0002 | c0002 | t0006 | g0057 | AFR | GWD | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03654 | hp2 | a0002 | c0002 | t0005 | g0115 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03688 | hp2 | a0002 | c0002 | t0005 | g0120 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03710 | hp1 | a0001 | c0001 | t0025 | g0267 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0172 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0071 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04199 | hp1 | a0002 | c0002 | t0005 | g0117 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04204 | hp2 | a0002 | c0002 | t0005 | g0118 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18522 | hp2 | a0001 | c0007 | t0014 | g0159 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18612 | hp1 | a0006 | c0010 | t0001 | g0140 | EAS | CHB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | CHB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0247 | EAS | CHB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18906 | hp1 | a0001 | c0001 | t0029 | g0154 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18906 | hp2 | a0001 | c0007 | t0014 | g0160 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18942 | hp1 | a0002 | c0002 | t0005 | g0040 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18944 | hp2 | a0001 | c0001 | t0012 | g0188 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18979 | hp2 | a0001 | c0001 | t0011 | g0187 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18983 | hp1 | a0001 | c0009 | t0001 | g0164 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19004 | hp2 | a0001 | c0001 | t0020 | g0137 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19030 | hp2 | a0002 | c0002 | t0004 | g0055 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19043 | hp1 | a0002 | c0002 | t0027 | g0056 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19060 | hp2 | a0001 | c0001 | t0012 | g0189 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19063 | hp1 | a0001 | c0001 | t0011 | g0245 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19078 | hp1 | a0001 | c0001 | t0016 | g0275 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19081 | hp2 | a0001 | c0001 | t0016 | g0276 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19091 | hp1 | a0001 | c0001 | t0026 | g0233 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA19240 | hp2 | a0002 | c0002 | t0005 | g0121 | AFR | YRI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ASW | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20129 | hp2 | a0002 | c0002 | t0006 | g0050 | AFR | ASW | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0072 | EUR | TSI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20805 | hp1 | a0001 | c0001 | t0028 | g0262 | EUR | TSI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | GIH | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02486 | hp1 | a0002 | c0002 | t0004 | g0053 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG03471 | hp2 | a0002 | c0002 | t0004 | g0061 | AFR | MSL | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG06807 | hp1 | a0001 | c0001 | t0032 | g0273 | AFR | USA | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | USA | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | USA | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | USA | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| NA21309 | hp2 | a0004 | c0004 | t0002 | g0088 | AFR | LWK | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0022 | g0086 | REF | REF | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0033 | g0272 | REF | REF | RASSF6_chr4_73566550_73625436 | RASSF6 | chr4 | 73566550 | 73625436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73576461
|
A | C | 1 | a0003 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.887T>G | p.Leu296Arg | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 10/11 | 1070/5882 | 887/1014 | 296/337 | chr4 | 73576461 | ||
| chr4:73576632
|
G | C | 1 | a0004 | 3 | HG00140.hp2 HG01943.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.821C>G | p.Ala274Gly | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/11 | 1004/5882 | 821/1014 | 274/337 | chr4 | 73576632 | ||
| chr4:73576707
|
T | A | 1 | a0006 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.746A>T | p.Asp249Val | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/11 | 929/5882 | 746/1014 | 249/337 | chr4 | 73576707 | ||
| chr4:73582213
|
T | C | 1 | a0005 | 2 | HG01070.hp1 HG01081.hp1 |
missense_variant | MODERATE | c.645A>G | p.Ile215Met | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/11 | 828/5882 | 645/1014 | 215/337 | chr4 | 73582213 | ||
| chr4:73585356
|
A | G | 4 | a0002a0003a0004others(1): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
missense_variant | MODERATE | c.391T>C | p.Ser131Pro | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/11 | 574/5882 | 391/1014 | 131/337 | chr4 | 73585356 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73576247
|
C | T | 1 | a0001c0009 | 1 | NA18983.hp1 | synonymous_variant | LOW | c.1002G>A | p.Glu334Glu | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1185/5882 | 1002/1014 | 334/337 | chr4 | 73576247 | ||
| chr4:73576469
|
T | C | 1 | a0001c0007 | 2 | NA18522.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.879A>G | p.Glu293Glu | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 10/11 | 1062/5882 | 879/1014 | 293/337 | chr4 | 73576469 | ||
| chr4:73585192
|
G | A | 1 | a0002c0008 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.555C>T | p.Phe185Phe | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/11 | 738/5882 | 555/1014 | 185/337 | chr4 | 73585192 | ||
| chr4:73587868
|
A | G | 1 | a0002c0005 | 2 | HG03491.hp1 HG03492.hp2 |
synonymous_variant | LOW | c.354T>C | p.Pro118Pro | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/11 | 537/5882 | 354/1014 | 118/337 | chr4 | 73587868 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73571914
|
G | T | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*4321C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 4321 | chr4 | 73571914 | |||||
| chr4:73571921
|
A | G | 1 | a0001c0001t0012 | 2 | NA18944.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4314T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 4314 | chr4 | 73571921 | |||||
| chr4:73572090
|
C | T | 1 | a0001c0001t0025 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4145G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 4145 | chr4 | 73572090 | |||||
| chr4:73572223
|
A | G | 2 | a0001c0001t0018a0001c0001t0019 | 2 | HG02004.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4012T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 4012 | chr4 | 73572223 | |||||
| chr4:73572267
|
C | T | 1 | a0002c0002t0023 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3968G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3968 | chr4 | 73572267 | |||||
| chr4:73572281
|
G | A | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(25): Show | 245 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*3954C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3954 | chr4 | 73572281 | |||||
| chr4:73572556
|
G | A | 6 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(3): Show | 43 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3679C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3679 | chr4 | 73572556 | |||||
| chr4:73572861
|
T | G | 7 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(4): Show | 45 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3374A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3374 | chr4 | 73572861 | |||||
| chr4:73573001
|
A | G | 2 | a0001c0001t0015a0001c0001t0031 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3234T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3234 | chr4 | 73573001 | |||||
| chr4:73573022
|
G | A | 1 | a0001c0001t0008 | 3 | HG00438.hp2 NA18747.hp1 NA18954.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3213C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3213 | chr4 | 73573022 | |||||
| chr4:73573057
|
C | T | 1 | a0002c0002t0022 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3178G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3178 | chr4 | 73573057 | |||||
| chr4:73573113
|
A | G | 1 | a0001c0001t0024 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3122T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3122 | chr4 | 73573113 | |||||
| chr4:73573177
|
G | T | 1 | a0001c0001t0011 | 2 | NA18979.hp2 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3058C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3058 | chr4 | 73573177 | |||||
| chr4:73573212
|
C | T | 8 | a0001c0001t0004a0001c0001t0007a0001c0001t0018others(5): Show | 32 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3023G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 3023 | chr4 | 73573212 | |||||
| chr4:73573251
|
C | T | 1 | a0002c0002t0027 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2984G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2984 | chr4 | 73573251 | |||||
| chr4:73573271
|
T | C | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(25): Show | 245 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2964A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2964 | chr4 | 73573271 | |||||
| chr4:73573671
|
T | A | 1 | a0001c0001t0015 | 2 | HG02895.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2564A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2564 | chr4 | 73573671 | |||||
| chr4:73573724
|
G | GTATT | 2 | a0001c0001t0015a0001c0001t0031 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2507_*2510dupAATA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2510 | chr4 | 73573724 | |||||
| chr4:73573807
|
G | A | 2 | a0002c0002t0009a0002c0005t0009 | 3 | HG02148.hp2 HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2428C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2428 | chr4 | 73573807 | |||||
| chr4:73573852
|
T | C | 1 | a0005c0006t0013 | 2 | HG01070.hp1 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2383A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2383 | chr4 | 73573852 | |||||
| chr4:73573940
|
C | A | 1 | a0001c0001t0018 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2295 | chr4 | 73573940 | |||||
| chr4:73573988
|
G | C | 1 | a0001c0001t0026 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2247C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 2247 | chr4 | 73573988 | |||||
| chr4:73574236
|
C | T | 1 | a0001c0001t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1999G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1999 | chr4 | 73574236 | |||||
| chr4:73574237
|
G | A | 1 | a0002c0002t0027 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1998C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1998 | chr4 | 73574237 | |||||
| chr4:73574535
|
T | A | 1 | a0001c0001t0017 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1700A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1700 | chr4 | 73574535 | |||||
| chr4:73574835
|
G | A | 13 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(10): Show | 70 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1400C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1400 | chr4 | 73574835 | |||||
| chr4:73575067
|
T | C | 13 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(10): Show | 70 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1168A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1168 | chr4 | 73575067 | |||||
| chr4:73575143
|
C | T | 3 | a0001c0001t0004a0002c0002t0004a0002c0008t0004 | 20 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1092G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1092 | chr4 | 73575143 | |||||
| chr4:73575180
|
T | G | 1 | a0001c0001t0028 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 1055 | chr4 | 73575180 | |||||
| chr4:73575356
|
A | G | 3 | a0001c0001t0007a0001c0001t0018a0001c0001t0019 | 5 | HG01070.hp2 HG01071.hp2 HG02004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*879T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 879 | chr4 | 73575356 | |||||
| chr4:73575415
|
C | T | 1 | a0001c0001t0020 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*820G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 820 | chr4 | 73575415 | |||||
| chr4:73575473
|
A | G | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*762T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 762 | chr4 | 73575473 | |||||
| chr4:73575502
|
T | C | 2 | a0001c0001t0015a0001c0001t0031 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*733A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 733 | chr4 | 73575502 | |||||
| chr4:73575536
|
A | C | 6 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(3): Show | 43 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*699T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 699 | chr4 | 73575536 | |||||
| chr4:73575586
|
G | C | 1 | a0001c0001t0030 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 649 | chr4 | 73575586 | |||||
| chr4:73575968
|
T | C | 2 | a0001c0001t0015a0001c0001t0031 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*267A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 267 | chr4 | 73575968 | |||||
| chr4:73575989
|
T | A | 1 | a0001c0001t0019 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 246 | chr4 | 73575989 | |||||
| chr4:73576056
|
A | G | 2 | a0001c0001t0015a0001c0001t0031 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*179T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 179 | chr4 | 73576056 | |||||
| chr4:73576069
|
A | G | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(11): Show | 71 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*166T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 166 | chr4 | 73576069 | |||||
| chr4:73576146
|
G | A | 2 | a0001c0001t0015a0001c0001t0031 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*89C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 11/11 | 89 | chr4 | 73576146 | |||||
| chr4:73611812
|
A | G | 3 | a0002c0002t0005a0002c0002t0010a0003c0003t0005 | 15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-17T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/11 | 17 | chr4 | 73611812 | |||||
| chr4:73620335
|
C | A | 1 | a0002c0002t0034 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/11 | 8540 | chr4 | 73620335 | |||||
| chr4:73620335
|
C | G | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
5_prime_UTR_variant | MODIFIER | c.-82G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/11 | 8540 | chr4 | 73620335 | |||||
| chr4:73620422
|
C | A | 1 | a0001c0001t0016 | 2 | NA19078.hp1 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-169G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/11 | 8627 | chr4 | 73620422 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:73576385
|
T | C | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.938+25A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 10/10 | chr4 | 73576385 | ||||||
| chr4:73576511
|
A | T | 1 | a0001c0001t0001g0035 | 2 | HG02135.hp1 NA19003.hp2 |
splice_region_variant&intron_variant | LOW | c.841-4T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/10 | chr4 | 73576511 | ||||||
| chr4:73576528
|
A | G | 1 | a0002c0002t0004g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.841-21T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/10 | chr4 | 73576528 | ||||||
| chr4:73576597
|
G | A | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.840+16C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 9/10 | chr4 | 73576597 | ||||||
| chr4:73576839
|
A | G | 1 | a0001c0001t0019g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.722-108T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73576839 | ||||||
| chr4:73576896
|
G | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-165C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73576896 | ||||||
| chr4:73576950
|
G | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.722-219C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73576950 | ||||||
| chr4:73576984
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.722-253G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73576984 | ||||||
| chr4:73577113
|
T | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.722-382A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577113 | ||||||
| chr4:73577296
|
T | C | 16 | a0001c0001t0004g0203a0002c0002t0004g0004a0002c0002t0004g0015others(13): Show | 20 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.722-565A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577296 | ||||||
| chr4:73577353
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.722-622G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577353 | ||||||
| chr4:73577523
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.722-792A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577523 | ||||||
| chr4:73577572
|
A | G | 1 | a0002c0002t0005g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.722-841T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577572 | ||||||
| chr4:73577574
|
T | C | 4 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0252others(1): Show | 4 | HG00408.hp2 HG02015.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-843A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577574 | ||||||
| chr4:73577586
|
C | T | 2 | a0005c0006t0013g0067a0005c0006t0013g0068 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.722-855G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577586 | ||||||
| chr4:73577606
|
T | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-875A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577606 | ||||||
| chr4:73577710
|
C | T | 5 | a0001c0001t0003g0029a0001c0001t0003g0163a0001c0001t0003g0174others(2): Show | 6 | HG00408.hp1 NA18974.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.722-979G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577710 | ||||||
| chr4:73577753
|
C | T | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1022G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577753 | ||||||
| chr4:73577902
|
T | G | 1 | a0001c0001t0001g0240 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.722-1171A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577902 | ||||||
| chr4:73577996
|
T | C | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.722-1265A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73577996 | ||||||
| chr4:73578020
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0235 | 2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.722-1289C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578020 | ||||||
| chr4:73578024
|
T | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1293A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578024 | ||||||
| chr4:73578029
|
T | TTTTCTTT others(17): Show |
3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1299_722-1298i others(26): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578029 | ||||||
| chr4:73578029
|
T | TTTTCTTT others(18): Show |
270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(267): Show | 332 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.722-1299_722-1298i others(27): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578029 | ||||||
| chr4:73578029
|
T | TTTTCTTT others(19): Show |
1 | a0001c0001t0001g0138 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.722-1299_722-1298i others(28): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578029 | ||||||
| chr4:73578030
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.722-1299C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578030 | ||||||
| chr4:73578031
|
A | AT | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1301_722-1300i others(3): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578031 | ||||||
| chr4:73578031
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.722-1300T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578031 | ||||||
| chr4:73578031
|
A | T | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(267): Show | 332 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.722-1300T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578031 | ||||||
| chr4:73578048
|
T | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1317A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578048 | ||||||
| chr4:73578071
|
T | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1340A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578071 | ||||||
| chr4:73578160
|
C | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 170 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.722-1429G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578160 | ||||||
| chr4:73578175
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0015g0157a0001c0001t0015g0158others(1): Show | 5 | HG01243.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.722-1444G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578175 | ||||||
| chr4:73578294
|
G | A | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1563C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578294 | ||||||
| chr4:73578544
|
G | C | 4 | a0001c0001t0002g0043a0001c0001t0015g0157a0001c0001t0015g0158others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-1813C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578544 | ||||||
| chr4:73578638
|
C | CT | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 166 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.722-1908dupA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578638 | ||||||
| chr4:73578656
|
C | T | 3 | a0001c0001t0008g0247a0001c0001t0008g0255a0001c0001t0008g0258 | 3 | HG00438.hp2 NA18747.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.722-1925G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578656 | ||||||
| chr4:73578694
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.722-1963G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578694 | ||||||
| chr4:73578721
|
G | C | 1 | a0001c0001t0003g0172 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.722-1990C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578721 | ||||||
| chr4:73578724
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.722-1993A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578724 | ||||||
| chr4:73578729
|
T | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-1998A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578729 | ||||||
| chr4:73578757
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0136 | 2 | NA18947.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.722-2026G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578757 | ||||||
| chr4:73578835
|
C | T | 1 | a0001c0001t0019g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.722-2104G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578835 | ||||||
| chr4:73578908
|
G | A | 15 | a0002c0002t0004g0004a0002c0002t0004g0015a0002c0002t0004g0044others(12): Show | 19 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.722-2177C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578908 | ||||||
| chr4:73578917
|
C | T | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-2186G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73578917 | ||||||
| chr4:73579083
|
C | T | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-2352G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579083 | ||||||
| chr4:73579142
|
G | A | 39 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(36): Show | 42 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.722-2411C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579142 | ||||||
| chr4:73579146
|
A | G | 1 | a0001c0001t0003g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.722-2415T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579146 | ||||||
| chr4:73579246
|
T | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-2515A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579246 | ||||||
| chr4:73579250
|
A | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.722-2519T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579250 | ||||||
| chr4:73579316
|
A | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2501T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579316 | ||||||
| chr4:73579376
|
G | A | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2441C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579376 | ||||||
| chr4:73579387
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.721+2430A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579387 | ||||||
| chr4:73579477
|
G | A | 1 | a0001c0001t0001g0030 | 2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.721+2340C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579477 | ||||||
| chr4:73579580
|
T | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2237A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579580 | ||||||
| chr4:73579581
|
G | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.721+2236C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579581 | ||||||
| chr4:73579626
|
C | T | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2191G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579626 | ||||||
| chr4:73579731
|
C | A | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+2086G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579731 | ||||||
| chr4:73579735
|
T | TA | 39 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(36): Show | 42 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.721+2081dupT | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579735 | ||||||
| chr4:73579979
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0167a0001c0001t0001g0242others(3): Show | 7 | NA18947.hp2 NA18970.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.721+1838C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73579979 | ||||||
| chr4:73580059
|
T | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+1758A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580059 | ||||||
| chr4:73580101
|
C | T | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+1716G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580101 | ||||||
| chr4:73580119
|
G | A | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.721+1698C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580119 | ||||||
| chr4:73580135
|
T | C | 1 | a0002c0002t0002g0106 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.721+1682A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580135 | ||||||
| chr4:73580143
|
A | G | 1 | a0002c0002t0027g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.721+1674T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580143 | ||||||
| chr4:73580218
|
A | C | 4 | a0001c0001t0001g0167a0001c0001t0015g0157a0001c0001t0015g0158others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.721+1599T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580218 | ||||||
| chr4:73580236
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.721+1581A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580236 | ||||||
| chr4:73580237
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.721+1580C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580237 | ||||||
| chr4:73580291
|
C | G | 10 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(7): Show | 10 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.721+1526G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580291 | ||||||
| chr4:73580328
|
A | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+1489T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580328 | ||||||
| chr4:73580451
|
G | A | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.721+1366C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580451 | ||||||
| chr4:73580454
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.721+1363A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580454 | ||||||
| chr4:73580518
|
A | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+1299T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580518 | ||||||
| chr4:73580691
|
A | G | 4 | a0001c0001t0007g0021a0001c0001t0007g0109a0001c0001t0018g0204others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.721+1126T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580691 | ||||||
| chr4:73580716
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.721+1101C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580716 | ||||||
| chr4:73580775
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(175): Show | 218 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.721+1042A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580775 | ||||||
| chr4:73580781
|
T | C | 1 | a0001c0001t0028g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.721+1036A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580781 | ||||||
| chr4:73580791
|
A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+1026T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580791 | ||||||
| chr4:73580806
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+1011G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580806 | ||||||
| chr4:73580879
|
G | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+938C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580879 | ||||||
| chr4:73580901
|
G | T | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.721+916C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580901 | ||||||
| chr4:73580908
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.721+909A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580908 | ||||||
| chr4:73580941
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 213 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.721+876G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580941 | ||||||
| chr4:73580970
|
A | T | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.721+847T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73580970 | ||||||
| chr4:73581071
|
A | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+746T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581071 | ||||||
| chr4:73581079
|
A | G | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(178): Show | 220 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.721+738T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581079 | ||||||
| chr4:73581105
|
G | GT | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 226 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.721+711dupA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581105 | ||||||
| chr4:73581166
|
A | G | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.721+651T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581166 | ||||||
| chr4:73581178
|
G | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+639C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581178 | ||||||
| chr4:73581274
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.721+543A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581274 | ||||||
| chr4:73581292
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.721+525A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581292 | ||||||
| chr4:73581305
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.721+512C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581305 | ||||||
| chr4:73581334
|
C | T | 6 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(3): Show | 6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.721+483G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581334 | ||||||
| chr4:73581387
|
C | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(139): Show | 178 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.721+430G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581387 | ||||||
| chr4:73581392
|
G | T | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.721+425C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581392 | ||||||
| chr4:73581700
|
C | G | 64 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0002g0041others(61): Show | 72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.721+117G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581700 | ||||||
| chr4:73581722
|
C | T | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.721+95G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581722 | ||||||
| chr4:73581735
|
C | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(199): Show | 246 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.721+82G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581735 | ||||||
| chr4:73581775
|
G | A | 45 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(42): Show | 48 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.721+42C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581775 | ||||||
| chr4:73581793
|
A | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(203): Show | 250 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.721+24T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 8/10 | chr4 | 73581793 | ||||||
| chr4:73581982
|
A | G | 1 | a0002c0002t0002g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.670-114T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/10 | chr4 | 73581982 | ||||||
| chr4:73581997
|
C | T | 6 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(3): Show | 6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-129G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/10 | chr4 | 73581997 | ||||||
| chr4:73582083
|
A | G | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.669+106T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/10 | chr4 | 73582083 | ||||||
| chr4:73582148
|
TATATA | T | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+36_669+40delTA others(3): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 7/10 | chr4 | 73582148 | ||||||
| chr4:73582361
|
ATCT | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.568-74_568-72delAG others(1): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582361 | ||||||
| chr4:73582417
|
TTTTG | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.568-131_568-128del others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582417 | ||||||
| chr4:73582486
|
A | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 7 | HG00544.hp1 HG02015.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.568-196T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582486 | ||||||
| chr4:73582590
|
T | C | 1 | a0001c0001t0003g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.568-300A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582590 | ||||||
| chr4:73582599
|
A | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.568-309T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582599 | ||||||
| chr4:73582623
|
A | T | 1 | a0002c0002t0034g0274 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.568-333T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582623 | ||||||
| chr4:73582634
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.568-344C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582634 | ||||||
| chr4:73582716
|
T | G | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.568-426A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582716 | ||||||
| chr4:73582839
|
A | AAC | 82 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(79): Show | 104 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.568-551_568-550dup others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582839 | ||||||
| chr4:73582839
|
A | AACAC | 6 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(3): Show | 6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-553_568-550dup others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582839 | ||||||
| chr4:73582843
|
C | A | 1 | a0001c0001t0030g0134 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.568-553G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582843 | ||||||
| chr4:73582844
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.568-554C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582844 | ||||||
| chr4:73582882
|
T | G | 2 | a0001c0001t0002g0041a0001c0001t0002g0054 | 2 | HG00323.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.568-592A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582882 | ||||||
| chr4:73582914
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.568-624C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582914 | ||||||
| chr4:73582921
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.568-631C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73582921 | ||||||
| chr4:73583008
|
G | A | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.568-718C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583008 | ||||||
| chr4:73583064
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.568-774A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583064 | ||||||
| chr4:73583070
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.568-780C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583070 | ||||||
| chr4:73583303
|
A | G | 2 | a0002c0002t0002g0020a0002c0002t0002g0101 | 3 | NA18964.hp1 NA18981.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.568-1013T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583303 | ||||||
| chr4:73583358
|
T | C | 6 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(3): Show | 6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-1068A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583358 | ||||||
| chr4:73583415
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.568-1125T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583415 | ||||||
| chr4:73583436
|
T | G | 3 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199 | 4 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-1146A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583436 | ||||||
| chr4:73583548
|
C | T | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.568-1258G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583548 | ||||||
| chr4:73583574
|
T | C | 3 | a0001c0001t0003g0184a0001c0001t0012g0188a0001c0001t0012g0189 | 3 | HG02135.hp2 NA18944.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.568-1284A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583574 | ||||||
| chr4:73583753
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+1427C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583753 | ||||||
| chr4:73583759
|
G | GTTC | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+1418_567+1420d others(5): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583759 | ||||||
| chr4:73583915
|
T | C | 7 | a0001c0001t0001g0038a0001c0001t0001g0229a0001c0001t0001g0237others(4): Show | 8 | HG00438.hp2 HG00621.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.567+1265A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583915 | ||||||
| chr4:73583976
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+1204G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73583976 | ||||||
| chr4:73584005
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+1175G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584005 | ||||||
| chr4:73584030
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+1150G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584030 | ||||||
| chr4:73584107
|
T | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+1073A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584107 | ||||||
| chr4:73584136
|
T | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+1044A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584136 | ||||||
| chr4:73584172
|
A | G | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+1008T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584172 | ||||||
| chr4:73584205
|
C | T | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.567+975G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584205 | ||||||
| chr4:73584211
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.567+969G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584211 | ||||||
| chr4:73584215
|
C | T | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.567+965G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584215 | ||||||
| chr4:73584334
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0260 | 2 | HG00733.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.567+846A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584334 | ||||||
| chr4:73584350
|
C | T | 38 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(35): Show | 41 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.567+830G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584350 | ||||||
| chr4:73584385
|
T | C | 2 | a0002c0002t0006g0045a0002c0002t0006g0046 | 2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.567+795A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584385 | ||||||
| chr4:73584522
|
A | G | 1 | a0002c0002t0002g0076 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.567+658T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584522 | ||||||
| chr4:73584591
|
T | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+589A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584591 | ||||||
| chr4:73584644
|
C | A | 1 | a0001c0001t0025g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.567+536G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584644 | ||||||
| chr4:73584645
|
G | A | 2 | a0002c0002t0005g0115a0002c0002t0005g0117 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.567+535C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584645 | ||||||
| chr4:73584647
|
T | A | 5 | a0002c0002t0002g0001a0002c0002t0002g0074a0002c0002t0002g0076others(2): Show | 10 | HG00733.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.567+533A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584647 | ||||||
| chr4:73584703
|
T | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+477A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584703 | ||||||
| chr4:73584773
|
T | G | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+407A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584773 | ||||||
| chr4:73584783
|
A | G | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+397T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584783 | ||||||
| chr4:73584849
|
G | A | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+331C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584849 | ||||||
| chr4:73584860
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+320C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584860 | ||||||
| chr4:73584937
|
T | A | 1 | a0002c0002t0027g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.567+243A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584937 | ||||||
| chr4:73584967
|
A | T | 2 | a0002c0002t0006g0045a0002c0002t0006g0046 | 2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.567+213T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73584967 | ||||||
| chr4:73585011
|
A | G | 82 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(79): Show | 104 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.567+169T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73585011 | ||||||
| chr4:73585046
|
G | T | 1 | a0002c0002t0002g0096 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.567+134C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73585046 | ||||||
| chr4:73585101
|
T | G | 1 | a0001c0001t0001g0259 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.567+79A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73585101 | ||||||
| chr4:73585113
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.567+67C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 6/10 | chr4 | 73585113 | ||||||
| chr4:73585375
|
T | G | 44 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0007others(41): Show | 53 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.383-11A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585375 | ||||||
| chr4:73585406
|
GTGTCCTA others(6): Show |
G | 1 | a0001c0001t0001g0234 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.383-55_383-43delGG others(11): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585406 | ||||||
| chr4:73585542
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.383-178G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585542 | ||||||
| chr4:73585638
|
TC | T | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.383-275delG | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585638 | ||||||
| chr4:73585829
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.383-465A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585829 | ||||||
| chr4:73585979
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.383-615G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73585979 | ||||||
| chr4:73586017
|
T | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.383-653A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586017 | ||||||
| chr4:73586200
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.383-836C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586200 | ||||||
| chr4:73586405
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.383-1041G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586405 | ||||||
| chr4:73586471
|
T | C | 82 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(79): Show | 104 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.383-1107A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586471 | ||||||
| chr4:73586500
|
C | T | 1 | a0001c0001t0019g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.383-1136G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586500 | ||||||
| chr4:73586516
|
A | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.383-1152T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586516 | ||||||
| chr4:73586520
|
T | C | 67 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(64): Show | 85 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.383-1156A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586520 | ||||||
| chr4:73586528
|
A | G | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.383-1164T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586528 | ||||||
| chr4:73586620
|
A | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+1220T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586620 | ||||||
| chr4:73586635
|
A | G | 1 | a0002c0002t0002g0072 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.382+1205T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586635 | ||||||
| chr4:73586640
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0021g0206 | 3 | HG02965.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.382+1200T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586640 | ||||||
| chr4:73586752
|
C | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+1088G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586752 | ||||||
| chr4:73586785
|
G | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+1055C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586785 | ||||||
| chr4:73586873
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+967G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586873 | ||||||
| chr4:73586889
|
G | A | 1 | a0002c0002t0004g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.382+951C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586889 | ||||||
| chr4:73586911
|
G | GAA | 78 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0007others(75): Show | 95 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.382+927_382+928dup others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586911 | ||||||
| chr4:73586911
|
G | GAAA | 8 | a0002c0002t0002g0001a0002c0002t0002g0069a0002c0002t0002g0072others(5): Show | 13 | HG00733.hp2 HG01257.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.382+926_382+928dup others(3): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73586911 | ||||||
| chr4:73587116
|
T | G | 1 | a0002c0002t0027g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+724A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587116 | ||||||
| chr4:73587134
|
G | A | 140 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0002g0041others(137): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.382+706C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587134 | ||||||
| chr4:73587137
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382+703G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587137 | ||||||
| chr4:73587142
|
T | G | 1 | a0001c0001t0003g0172 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382+698A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587142 | ||||||
| chr4:73587144
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382+696A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587144 | ||||||
| chr4:73587217
|
C | T | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.382+623G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587217 | ||||||
| chr4:73587234
|
A | G | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.382+606T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587234 | ||||||
| chr4:73587277
|
G | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+563C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587277 | ||||||
| chr4:73587318
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+522G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587318 | ||||||
| chr4:73587347
|
T | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+493A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587347 | ||||||
| chr4:73587394
|
T | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+446A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587394 | ||||||
| chr4:73587428
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+412G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587428 | ||||||
| chr4:73587493
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+347C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587493 | ||||||
| chr4:73587595
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 169 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.382+245C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587595 | ||||||
| chr4:73587687
|
T | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.382+153A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587687 | ||||||
| chr4:73587730
|
G | A | 6 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(3): Show | 6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+110C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587730 | ||||||
| chr4:73587820
|
A | C | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.382+20T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 5/10 | chr4 | 73587820 | ||||||
| chr4:73587939
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
splice_region_variant&intron_variant | LOW | c.288-5C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73587939 | ||||||
| chr4:73587974
|
T | C | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.288-40A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73587974 | ||||||
| chr4:73588010
|
A | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.288-76T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588010 | ||||||
| chr4:73588065
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 169 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.288-131T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588065 | ||||||
| chr4:73588110
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.288-176T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588110 | ||||||
| chr4:73588140
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(128): Show | 167 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.288-206A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588140 | ||||||
| chr4:73588160
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.288-226G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588160 | ||||||
| chr4:73588161
|
G | A | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.288-227C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588161 | ||||||
| chr4:73588271
|
A | G | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.288-337T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588271 | ||||||
| chr4:73588287
|
C | T | 88 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(85): Show | 110 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.288-353G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588287 | ||||||
| chr4:73588379
|
T | C | 1 | a0006c0010t0001g0140 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.288-445A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588379 | ||||||
| chr4:73588649
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 168 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.288-715T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588649 | ||||||
| chr4:73588675
|
T | G | 39 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(36): Show | 42 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.288-741A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588675 | ||||||
| chr4:73588766
|
T | A | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.288-832A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588766 | ||||||
| chr4:73588783
|
G | A | 6 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(3): Show | 6 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.288-849C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | ||||||
| chr4:73588783
|
G | GTCATCA | 52 | a0001c0001t0001g0131a0001c0001t0001g0221a0001c0001t0001g0238others(49): Show | 62 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.288-855_288-850dup others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | ||||||
| chr4:73588783
|
G | GTCATCAT others(2): Show |
160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.288-858_288-850dup others(9): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | ||||||
| chr4:73588783
|
G | GTCATCAT others(5): Show |
18 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0126others(15): Show | 19 | HG00741.hp2 HG01358.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-861_288-850dup others(12): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | ||||||
| chr4:73588783
|
G | GTCATCAT others(8): Show |
29 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(26): Show | 32 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.288-864_288-850dup others(15): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | ||||||
| chr4:73588783
|
G | GTCATCAT others(11): Show |
2 | a0001c0001t0003g0172a0001c0001t0012g0189 | 2 | HG03831.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.288-867_288-850dup others(18): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588783 | ||||||
| chr4:73588913
|
C | G | 1 | a0002c0002t0004g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.288-979G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588913 | ||||||
| chr4:73588996
|
G | A | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1062C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73588996 | ||||||
| chr4:73589053
|
G | A | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1119C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589053 | ||||||
| chr4:73589144
|
T | G | 60 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(57): Show | 67 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.288-1210A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589144 | ||||||
| chr4:73589420
|
A | G | 1 | a0002c0002t0027g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.288-1486T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589420 | ||||||
| chr4:73589500
|
G | A | 7 | a0001c0001t0019g0124a0002c0002t0006g0045a0002c0002t0006g0046others(4): Show | 7 | HG02004.hp2 HG02145.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-1566C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589500 | ||||||
| chr4:73589510
|
G | A | 2 | a0002c0002t0002g0020a0002c0002t0002g0101 | 3 | NA18964.hp1 NA18981.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.288-1576C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589510 | ||||||
| chr4:73589640
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.288-1706C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589640 | ||||||
| chr4:73589664
|
A | G | 54 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(51): Show | 61 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.288-1730T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589664 | ||||||
| chr4:73589757
|
C | A | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1823G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589757 | ||||||
| chr4:73589821
|
T | C | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1887A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589821 | ||||||
| chr4:73589847
|
A | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.288-1913T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589847 | ||||||
| chr4:73589909
|
C | T | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-1975G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589909 | ||||||
| chr4:73589911
|
G | A | 39 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(36): Show | 42 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.288-1977C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589911 | ||||||
| chr4:73589933
|
C | T | 1 | a0001c0001t0031g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.288-1999G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73589933 | ||||||
| chr4:73590003
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.288-2069G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590003 | ||||||
| chr4:73590037
|
T | A | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.288-2103A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590037 | ||||||
| chr4:73590057
|
A | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(127): Show | 166 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.288-2123T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590057 | ||||||
| chr4:73590123
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.288-2189A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590123 | ||||||
| chr4:73590152
|
T | C | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.288-2218A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590152 | ||||||
| chr4:73590232
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.288-2298A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590232 | ||||||
| chr4:73590339
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.288-2405C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590339 | ||||||
| chr4:73590488
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.288-2554A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590488 | ||||||
| chr4:73590655
|
T | C | 2 | a0002c0002t0004g0049a0002c0002t0004g0060 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.288-2721A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590655 | ||||||
| chr4:73590998
|
G | T | 1 | a0001c0001t0032g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287+2453C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73590998 | ||||||
| chr4:73591102
|
C | T | 1 | a0001c0001t0032g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287+2349G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591102 | ||||||
| chr4:73591126
|
A | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 168 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.287+2325T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591126 | ||||||
| chr4:73591127
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+2324C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591127 | ||||||
| chr4:73591143
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 7 | HG00544.hp1 HG02015.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+2308G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591143 | ||||||
| chr4:73591161
|
A | G | 54 | a0001c0001t0001g0025a0001c0001t0001g0171a0001c0001t0003g0028others(51): Show | 61 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.287+2290T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591161 | ||||||
| chr4:73591618
|
AG | A | 5 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(2): Show | 5 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+1832delC | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591618 | ||||||
| chr4:73591723
|
G | A | 1 | a0002c0002t0023g0099 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.287+1728C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591723 | ||||||
| chr4:73591754
|
G | C | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.287+1697C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591754 | ||||||
| chr4:73591779
|
C | T | 2 | a0005c0006t0013g0067a0005c0006t0013g0068 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.287+1672G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591779 | ||||||
| chr4:73591854
|
G | A | 1 | a0002c0002t0027g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.287+1597C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73591854 | ||||||
| chr4:73592313
|
G | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.287+1138C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592313 | ||||||
| chr4:73592410
|
C | T | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.287+1041G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592410 | ||||||
| chr4:73592506
|
T | G | 19 | a0001c0001t0007g0021a0001c0001t0007g0109a0001c0001t0019g0124others(16): Show | 24 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.287+945A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592506 | ||||||
| chr4:73592730
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.287+721T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592730 | ||||||
| chr4:73592824
|
T | C | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.287+627A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592824 | ||||||
| chr4:73592985
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.287+466T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592985 | ||||||
| chr4:73592992
|
G | T | 15 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199others(12): Show | 19 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.287+459C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73592992 | ||||||
| chr4:73593019
|
AT | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(208): Show | 266 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.287+431delA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593019 | ||||||
| chr4:73593019
|
ATT | A | 58 | a0001c0001t0001g0025a0001c0001t0001g0143a0001c0001t0001g0171others(55): Show | 65 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.287+430_287+431del others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593019 | ||||||
| chr4:73593080
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.287+371T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593080 | ||||||
| chr4:73593172
|
C | T | 1 | a0002c0002t0006g0050 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.287+279G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593172 | ||||||
| chr4:73593270
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(55): Show | 77 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.287+181G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593270 | ||||||
| chr4:73593305
|
C | A | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.287+146G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593305 | ||||||
| chr4:73593389
|
C | T | 1 | a0002c0002t0004g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.287+62G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 4/10 | chr4 | 73593389 | ||||||
| chr4:73593945
|
T | C | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.145-352A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73593945 | ||||||
| chr4:73594037
|
A | T | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.145-444T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594037 | ||||||
| chr4:73594072
|
G | A | 1 | a0002c0002t0002g0082 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.145-479C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594072 | ||||||
| chr4:73594185
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.145-592T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594185 | ||||||
| chr4:73594261
|
A | T | 52 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(49): Show | 66 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.145-668T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594261 | ||||||
| chr4:73594302
|
C | G | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | NA18964.hp2 NA18971.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-709G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594302 | ||||||
| chr4:73594435
|
C | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.145-842G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594435 | ||||||
| chr4:73594449
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.145-856T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594449 | ||||||
| chr4:73594571
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(164): Show | 206 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.145-978G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73594571 | ||||||
| chr4:73595027
|
A | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(164): Show | 206 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.145-1434T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595027 | ||||||
| chr4:73595060
|
T | A | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.145-1467A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595060 | ||||||
| chr4:73595110
|
G | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(55): Show | 77 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.145-1517C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595110 | ||||||
| chr4:73595207
|
G | A | 3 | a0001c0001t0001g0231a0001c0001t0001g0249a0001c0001t0024g0224 | 3 | HG02572.hp1 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.145-1614C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595207 | ||||||
| chr4:73595226
|
G | A | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.145-1633C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595226 | ||||||
| chr4:73595236
|
C | T | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.145-1643G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595236 | ||||||
| chr4:73595429
|
T | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.145-1836A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595429 | ||||||
| chr4:73595446
|
G | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.145-1853C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595446 | ||||||
| chr4:73595456
|
C | T | 1 | a0002c0002t0002g0070 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.145-1863G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595456 | ||||||
| chr4:73595462
|
G | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.145-1869C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595462 | ||||||
| chr4:73595468
|
G | C | 2 | a0001c0007t0014g0159a0001c0007t0014g0160 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.145-1875C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595468 | ||||||
| chr4:73595590
|
T | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.145-1997A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595590 | ||||||
| chr4:73595707
|
G | A | 12 | a0002c0002t0005g0022a0002c0002t0005g0040a0002c0002t0005g0115others(9): Show | 15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.145-2114C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595707 | ||||||
| chr4:73595711
|
ATATT | A | 79 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(76): Show | 97 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.145-2122_145-2119d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595711 | ||||||
| chr4:73595729
|
C | T | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.145-2136G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595729 | ||||||
| chr4:73595791
|
A | T | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.145-2198T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595791 | ||||||
| chr4:73595818
|
G | A | 2 | a0001c0001t0019g0124a0001c0001t0029g0154 | 2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.145-2225C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595818 | ||||||
| chr4:73595927
|
G | A | 1 | a0001c0001t0025g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.145-2334C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595927 | ||||||
| chr4:73595993
|
A | C | 1 | a0001c0001t0003g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145-2400T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73595993 | ||||||
| chr4:73596053
|
C | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.145-2460G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596053 | ||||||
| chr4:73596210
|
A | AGATGACA others(315): Show |
1 | a0001c0001t0001g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.144+2429_144+2430i others(324): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596210 | ||||||
| chr4:73596298
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.144+2342A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596298 | ||||||
| chr4:73596550
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(164): Show | 206 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.144+2090G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596550 | ||||||
| chr4:73596694
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.144+1946C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596694 | ||||||
| chr4:73596902
|
G | A | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.144+1738C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73596902 | ||||||
| chr4:73597191
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.144+1449G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597191 | ||||||
| chr4:73597221
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.144+1419G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597221 | ||||||
| chr4:73597362
|
T | G | 4 | a0001c0001t0001g0231a0001c0001t0001g0249a0001c0001t0018g0204others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+1278A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597362 | ||||||
| chr4:73597392
|
T | C | 1 | a0002c0002t0005g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.144+1248A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597392 | ||||||
| chr4:73597667
|
C | A | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.144+973G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597667 | ||||||
| chr4:73597866
|
T | C | 1 | a0001c0001t0003g0190 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.144+774A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597866 | ||||||
| chr4:73597880
|
C | T | 20 | a0001c0001t0007g0021a0001c0001t0007g0109a0001c0001t0019g0124others(17): Show | 25 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.144+760G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597880 | ||||||
| chr4:73597883
|
T | A | 7 | a0001c0001t0003g0029a0001c0001t0003g0163a0001c0001t0003g0174others(4): Show | 8 | HG00408.hp1 NA18974.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.144+757A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73597883 | ||||||
| chr4:73598057
|
AACC | A | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.144+580_144+582del others(3): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598057 | ||||||
| chr4:73598068
|
C | T | 79 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(76): Show | 97 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.144+572G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598068 | ||||||
| chr4:73598405
|
C | A | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0051others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+235G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598405 | ||||||
| chr4:73598405
|
C | T | 4 | a0001c0001t0001g0231a0001c0001t0001g0249a0001c0001t0018g0204others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+235G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598405 | ||||||
| chr4:73598423
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144+217A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598423 | ||||||
| chr4:73598568
|
T | TTG | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(240): Show | 300 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.144+70_144+71dupCA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598568 | ||||||
| chr4:73598568
|
T | TTGTG | 15 | a0002c0002t0002g0026a0002c0002t0002g0199a0002c0002t0005g0022others(12): Show | 19 | HG01123.hp1 HG01433.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.144+68_144+71dupCA others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598568 | ||||||
| chr4:73598568
|
T | TTGTGTG | 4 | a0001c0001t0007g0021a0001c0001t0007g0109a0001c0001t0019g0124others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+66_144+71dupCA others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598568 | ||||||
| chr4:73598585
|
T | C | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0051others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+55A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 3/10 | chr4 | 73598585 | ||||||
| chr4:73598726
|
TA | T | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.66-9delT | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73598726 | ||||||
| chr4:73598839
|
T | C | 1 | a0002c0002t0002g0019 | 2 | HG01099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.66-121A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73598839 | ||||||
| chr4:73599210
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.66-492C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599210 | ||||||
| chr4:73599278
|
C | T | 20 | a0002c0002t0004g0004a0002c0002t0004g0015a0002c0002t0004g0044others(17): Show | 24 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.66-560G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599278 | ||||||
| chr4:73599369
|
C | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.66-651G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599369 | ||||||
| chr4:73599754
|
C | A | 1 | a0001c0001t0001g0036 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.66-1036G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599754 | ||||||
| chr4:73599906
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.66-1188A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73599906 | ||||||
| chr4:73600106
|
C | CTTCTCCC others(12): Show |
1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.66-1407_66-1389dup others(19): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600106 | ||||||
| chr4:73600160
|
A | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.66-1442T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600160 | ||||||
| chr4:73600176
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.66-1458G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600176 | ||||||
| chr4:73600317
|
C | T | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.66-1599G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600317 | ||||||
| chr4:73600415
|
T | C | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.66-1697A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600415 | ||||||
| chr4:73600499
|
G | A | 1 | a0001c0001t0001g0024 | 2 | NA19010.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.66-1781C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600499 | ||||||
| chr4:73600568
|
C | G | 2 | a0001c0007t0014g0159a0001c0007t0014g0160 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.66-1850G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600568 | ||||||
| chr4:73600609
|
T | C | 4 | a0002c0002t0001g0095a0002c0002t0009g0078a0002c0005t0009g0083others(1): Show | 4 | HG02148.hp2 HG02273.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.66-1891A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600609 | ||||||
| chr4:73600692
|
G | A | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.66-1974C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600692 | ||||||
| chr4:73600702
|
A | T | 44 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0007others(41): Show | 53 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.66-1984T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600702 | ||||||
| chr4:73600718
|
C | G | 1 | a0002c0002t0005g0115 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.66-2000G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600718 | ||||||
| chr4:73600727
|
T | TA | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.66-2010dupT | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600727 | ||||||
| chr4:73600803
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.66-2085C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600803 | ||||||
| chr4:73600863
|
A | G | 2 | a0001c0007t0014g0159a0001c0007t0014g0160 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.66-2145T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600863 | ||||||
| chr4:73600918
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66-2200C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600918 | ||||||
| chr4:73600925
|
T | A | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.66-2207A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600925 | ||||||
| chr4:73600941
|
C | T | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.66-2223G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600941 | ||||||
| chr4:73600999
|
T | C | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.66-2281A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73600999 | ||||||
| chr4:73601202
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.66-2484T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73601202 | ||||||
| chr4:73601548
|
A | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0169others(7): Show | 12 | HG01358.hp1 HG01496.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.66-2830T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73601548 | ||||||
| chr4:73601628
|
T | C | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.66-2910A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73601628 | ||||||
| chr4:73601689
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.66-2971G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73601689 | ||||||
| chr4:73602101
|
A | G | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.66-3383T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602101 | ||||||
| chr4:73602204
|
C | T | 12 | a0002c0002t0005g0022a0002c0002t0005g0040a0002c0002t0005g0115others(9): Show | 15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.66-3486G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602204 | ||||||
| chr4:73602569
|
A | G | 1 | a0002c0002t0002g0085 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.66-3851T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602569 | ||||||
| chr4:73602590
|
C | CTAAG | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.66-3873_66-3872ins others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602590 | ||||||
| chr4:73602782
|
C | T | 3 | a0001c0001t0003g0168a0001c0001t0003g0177a0001c0001t0017g0178 | 3 | HG00639.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.66-4064G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602782 | ||||||
| chr4:73602811
|
A | G | 5 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(2): Show | 5 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.66-4093T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73602811 | ||||||
| chr4:73603092
|
G | GAAGA | 12 | a0002c0002t0005g0022a0002c0002t0005g0040a0002c0002t0005g0115others(9): Show | 15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.66-4378_66-4375dup others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603092 | ||||||
| chr4:73603266
|
G | A | 1 | a0001c0001t0003g0198 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.66-4548C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603266 | ||||||
| chr4:73603584
|
C | T | 2 | a0001c0001t0019g0124a0001c0001t0029g0154 | 2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.66-4866G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603584 | ||||||
| chr4:73603804
|
G | C | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.66-5086C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603804 | ||||||
| chr4:73603870
|
A | T | 1 | a0002c0002t0027g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.66-5152T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603870 | ||||||
| chr4:73603936
|
T | C | 2 | a0001c0001t0003g0163a0001c0001t0003g0202 | 2 | NA18983.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.66-5218A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73603936 | ||||||
| chr4:73604240
|
C | A | 1 | a0001c0001t0003g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.66-5522G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604240 | ||||||
| chr4:73604241
|
G | A | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.66-5523C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604241 | ||||||
| chr4:73604276
|
C | T | 1 | a0002c0002t0002g0094 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.66-5558G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604276 | ||||||
| chr4:73604288
|
C | T | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.66-5570G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604288 | ||||||
| chr4:73604461
|
G | A | 4 | a0002c0002t0001g0095a0002c0002t0009g0078a0002c0005t0009g0083others(1): Show | 4 | HG02148.hp2 HG02273.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.66-5743C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604461 | ||||||
| chr4:73604468
|
T | C | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.66-5750A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604468 | ||||||
| chr4:73604474
|
A | AAAAAC | 9 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0196others(6): Show | 11 | HG01243.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.66-5761_66-5757dup others(5): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604474 | ||||||
| chr4:73604490
|
A | C | 5 | a0002c0002t0006g0045a0002c0002t0006g0046a0002c0002t0006g0050others(2): Show | 5 | HG02145.hp1 HG03130.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.66-5772T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604490 | ||||||
| chr4:73604864
|
C | A | 1 | a0002c0002t0027g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.66-6146G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604864 | ||||||
| chr4:73604884
|
C | CT | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(117): Show | 153 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.66-6167dupA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604884 | ||||||
| chr4:73604920
|
G | A | 1 | a0002c0002t0002g0100 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.66-6202C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73604920 | ||||||
| chr4:73605215
|
G | A | 1 | a0002c0002t0002g0093 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.66-6497C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605215 | ||||||
| chr4:73605260
|
C | T | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG00323.hp2 HG02258.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.65+6471G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605260 | ||||||
| chr4:73605608
|
T | G | 2 | a0002c0002t0002g0069a0002c0002t0002g0072 | 2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.65+6123A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605608 | ||||||
| chr4:73605614
|
G | A | 1 | a0002c0002t0004g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.65+6117C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605614 | ||||||
| chr4:73605615
|
A | C | 1 | a0002c0002t0004g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.65+6116T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605615 | ||||||
| chr4:73605881
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(35): Show | 49 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.65+5850T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605881 | ||||||
| chr4:73605998
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.65+5733G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73605998 | ||||||
| chr4:73606021
|
C | G | 4 | a0001c0001t0002g0042a0001c0001t0002g0051a0001c0001t0002g0052others(1): Show | 4 | HG02258.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.65+5710G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606021 | ||||||
| chr4:73606194
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.65+5537T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606194 | ||||||
| chr4:73606227
|
T | C | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+5504A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606227 | ||||||
| chr4:73606280
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0054 | 2 | HG00323.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.65+5451G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606280 | ||||||
| chr4:73606364
|
C | T | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+5367G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606364 | ||||||
| chr4:73606397
|
A | G | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65+5334T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606397 | ||||||
| chr4:73606434
|
C | G | 3 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0107 | 3 | HG02083.hp1 NA18985.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.65+5297G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606434 | ||||||
| chr4:73606496
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.65+5235G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606496 | ||||||
| chr4:73606551
|
G | A | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(131): Show | 163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.65+5180C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606551 | ||||||
| chr4:73606639
|
GT | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(122): Show | 157 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.65+5091delA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606639 | ||||||
| chr4:73606639
|
GTT | G | 7 | a0001c0001t0002g0041a0001c0001t0002g0054a0001c0001t0003g0144others(4): Show | 8 | HG00323.hp2 HG01069.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.65+5090_65+5091del others(2): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606639 | ||||||
| chr4:73606639
|
GTTTTTT | G | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+5086_65+5091del others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73606639 | ||||||
| chr4:73607066
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65+4665A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607066 | ||||||
| chr4:73607089
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65+4642A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607089 | ||||||
| chr4:73607119
|
G | C | 1 | a0001c0001t0003g0192 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.65+4612C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607119 | ||||||
| chr4:73607159
|
A | G | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+4572T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607159 | ||||||
| chr4:73607179
|
A | G | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(133): Show | 165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.65+4552T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607179 | ||||||
| chr4:73607197
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65+4534A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607197 | ||||||
| chr4:73607419
|
C | T | 15 | a0001c0001t0007g0021a0001c0001t0007g0109a0002c0002t0005g0022others(12): Show | 19 | HG01070.hp2 HG01071.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.65+4312G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607419 | ||||||
| chr4:73607598
|
G | A | 12 | a0002c0002t0005g0022a0002c0002t0005g0040a0002c0002t0005g0115others(9): Show | 15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.65+4133C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607598 | ||||||
| chr4:73607722
|
T | C | 1 | a0002c0002t0004g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65+4009A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607722 | ||||||
| chr4:73607729
|
TA | T | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.65+4001delT | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607729 | ||||||
| chr4:73607734
|
AACCCTCC | A | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.65+3990_65+3996del others(7): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607734 | ||||||
| chr4:73607740
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3991G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607740 | ||||||
| chr4:73607741
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3990G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607741 | ||||||
| chr4:73607742
|
A | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.65+3989T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607742 | ||||||
| chr4:73607753
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65+3978G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607753 | ||||||
| chr4:73607757
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.65+3974T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607757 | ||||||
| chr4:73607766
|
T | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3965A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607766 | ||||||
| chr4:73607780
|
T | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3951A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607780 | ||||||
| chr4:73607784
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3947T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607784 | ||||||
| chr4:73607785
|
T | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3946A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607785 | ||||||
| chr4:73607789
|
A | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3942T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607789 | ||||||
| chr4:73607793
|
T | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3938A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607793 | ||||||
| chr4:73607795
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3936G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607795 | ||||||
| chr4:73607801
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3930T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607801 | ||||||
| chr4:73607805
|
G | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3926C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607805 | ||||||
| chr4:73607811
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3920G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607811 | ||||||
| chr4:73607813
|
ACCTCCTC others(22): Show |
A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3889_65+3917del others(29): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607813 | ||||||
| chr4:73607814
|
C | A | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.65+3917G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607814 | ||||||
| chr4:73607843
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3888G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607843 | ||||||
| chr4:73607845
|
T | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3886A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607845 | ||||||
| chr4:73607846
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3885T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607846 | ||||||
| chr4:73607848
|
C | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3883G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607848 | ||||||
| chr4:73607849
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3882G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607849 | ||||||
| chr4:73607850
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.65+3881G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607850 | ||||||
| chr4:73607858
|
T | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3873A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607858 | ||||||
| chr4:73607861
|
T | C | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3870A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607861 | ||||||
| chr4:73607862
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3869G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607862 | ||||||
| chr4:73607863
|
T | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3868A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607863 | ||||||
| chr4:73607864
|
T | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3867A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607864 | ||||||
| chr4:73607866
|
T | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3865A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607866 | ||||||
| chr4:73607868
|
C | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3863G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607868 | ||||||
| chr4:73607869
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3862G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607869 | ||||||
| chr4:73607879
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3852G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607879 | ||||||
| chr4:73607880
|
T | C | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3851A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607880 | ||||||
| chr4:73607889
|
ACCCCTCC others(61): Show |
A | 1 | a0002c0002t0002g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.65+3774_65+3841del others(68): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607889 | ||||||
| chr4:73607895
|
C | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3836G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607895 | ||||||
| chr4:73607899
|
T | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3832A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607899 | ||||||
| chr4:73607902
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3829G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607902 | ||||||
| chr4:73607904
|
T | C | 3 | a0001c0001t0003g0163a0001c0001t0003g0175a0001c0001t0003g0193 | 3 | NA18960.hp2 NA18983.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.65+3827A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607904 | ||||||
| chr4:73607905
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3826G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607905 | ||||||
| chr4:73607907
|
T | G | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3824A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607907 | ||||||
| chr4:73607974
|
CTCTCTAC others(6): Show |
C | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3744_65+3756del others(13): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607974 | ||||||
| chr4:73607987
|
TTCCTCTC others(8): Show |
T | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(268): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.65+3729_65+3743del others(15): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607987 | ||||||
| chr4:73607994
|
C | A | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3737G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607994 | ||||||
| chr4:73607996
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3735G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73607996 | ||||||
| chr4:73608015
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3716G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608015 | ||||||
| chr4:73608016
|
T | C | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3715A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608016 | ||||||
| chr4:73608017
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65+3714G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608017 | ||||||
| chr4:73608143
|
G | A | 48 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(45): Show | 54 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.65+3588C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608143 | ||||||
| chr4:73608144
|
C | A | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.65+3587G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608144 | ||||||
| chr4:73608409
|
A | G | 2 | a0001c0001t0019g0124a0001c0001t0029g0154 | 2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.65+3322T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608409 | ||||||
| chr4:73608547
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(35): Show | 49 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.65+3184T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608547 | ||||||
| chr4:73608760
|
T | C | 1 | a0002c0002t0004g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65+2971A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608760 | ||||||
| chr4:73608780
|
G | A | 1 | a0002c0002t0002g0066 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.65+2951C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608780 | ||||||
| chr4:73608836
|
T | C | 12 | a0002c0002t0005g0022a0002c0002t0005g0040a0002c0002t0005g0115others(9): Show | 15 | HG02027.hp1 HG02056.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.65+2895A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73608836 | ||||||
| chr4:73609152
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.65+2579T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609152 | ||||||
| chr4:73609168
|
T | C | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.65+2563A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609168 | ||||||
| chr4:73609377
|
A | T | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65+2354T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609377 | ||||||
| chr4:73609534
|
A | T | 2 | a0001c0001t0019g0124a0001c0001t0029g0154 | 2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.65+2197T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609534 | ||||||
| chr4:73609542
|
C | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.65+2189G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609542 | ||||||
| chr4:73609703
|
G | A | 1 | a0002c0002t0004g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65+2028C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609703 | ||||||
| chr4:73609752
|
C | T | 2 | a0001c0001t0019g0124a0001c0001t0029g0154 | 2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.65+1979G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609752 | ||||||
| chr4:73609792
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0264 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.65+1939G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609792 | ||||||
| chr4:73609897
|
T | C | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.65+1834A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73609897 | ||||||
| chr4:73610077
|
C | T | 52 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(49): Show | 66 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.65+1654G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610077 | ||||||
| chr4:73610078
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.65+1653C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610078 | ||||||
| chr4:73610149
|
C | A | 1 | a0001c0001t0003g0176 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.65+1582G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610149 | ||||||
| chr4:73610203
|
C | A | 2 | a0002c0002t0010g0122a0002c0002t0010g0123 | 2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.65+1528G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610203 | ||||||
| chr4:73610689
|
C | T | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65+1042G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610689 | ||||||
| chr4:73610809
|
T | C | 1 | a0001c0001t0028g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.65+922A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610809 | ||||||
| chr4:73610948
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65+783G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610948 | ||||||
| chr4:73610986
|
C | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.65+745G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73610986 | ||||||
| chr4:73611110
|
T | A | 1 | a0001c0001t0002g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.65+621A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611110 | ||||||
| chr4:73611165
|
C | T | 1 | a0001c0001t0001g0024 | 2 | NA19010.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.65+566G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611165 | ||||||
| chr4:73611207
|
A | G | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(134): Show | 167 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.65+524T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611207 | ||||||
| chr4:73611276
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65+455G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611276 | ||||||
| chr4:73611306
|
A | G | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.65+425T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611306 | ||||||
| chr4:73611418
|
T | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(132): Show | 164 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.65+313A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611418 | ||||||
| chr4:73611475
|
T | G | 19 | a0002c0002t0004g0004a0002c0002t0004g0015a0002c0002t0004g0044others(16): Show | 23 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.65+256A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611475 | ||||||
| chr4:73611663
|
A | C | 1 | a0002c0002t0002g0091 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.65+68T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611663 | ||||||
| chr4:73611703
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0270 | 2 | NA18964.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.65+28G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 2/10 | chr4 | 73611703 | ||||||
| chr4:73612100
|
T | G | 2 | a0001c0001t0019g0124a0001c0001t0029g0154 | 2 | HG02004.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-34-271A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612100 | ||||||
| chr4:73612122
|
G | T | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-34-293C>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612122 | ||||||
| chr4:73612184
|
G | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-34-355C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612184 | ||||||
| chr4:73612358
|
A | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-34-529T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612358 | ||||||
| chr4:73612377
|
C | A | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-34-548G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612377 | ||||||
| chr4:73612483
|
T | TC | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(157): Show | 203 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.-34-655_-34-654ins others(1): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612483 | ||||||
| chr4:73612484
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(103): Show | 125 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-34-655A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612484 | ||||||
| chr4:73612492
|
TTTTAAAA | T | 48 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(45): Show | 54 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-34-670_-34-664del others(7): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612492 | ||||||
| chr4:73612496
|
A | T | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(222): Show | 281 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.-34-667T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612496 | ||||||
| chr4:73612497
|
A | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(221): Show | 280 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.-34-668T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612497 | ||||||
| chr4:73612498
|
A | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(221): Show | 280 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.-34-669T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612498 | ||||||
| chr4:73612499
|
A | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(195): Show | 249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.-34-670T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612499 | ||||||
| chr4:73612634
|
A | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0265 | 5 | HG01257.hp2 HG02735.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-805T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612634 | ||||||
| chr4:73612685
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(36): Show | 50 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-34-856T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612685 | ||||||
| chr4:73612831
|
A | C | 1 | a0001c0001t0001g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34-1002T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612831 | ||||||
| chr4:73612908
|
C | G | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-34-1079G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73612908 | ||||||
| chr4:73613004
|
G | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-34-1175C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613004 | ||||||
| chr4:73613170
|
T | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-34-1341A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613170 | ||||||
| chr4:73613464
|
T | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(252): Show | 313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.-34-1635A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613464 | ||||||
| chr4:73613532
|
G | A | 5 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0051others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-1703C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613532 | ||||||
| chr4:73613663
|
C | A | 1 | a0001c0001t0003g0194 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-34-1834G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613663 | ||||||
| chr4:73613997
|
C | T | 1 | a0002c0002t0002g0106 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-34-2168G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73613997 | ||||||
| chr4:73614237
|
T | C | 1 | a0001c0001t0032g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-34-2408A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614237 | ||||||
| chr4:73614302
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-34-2473G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614302 | ||||||
| chr4:73614725
|
G | A | 1 | a0002c0002t0002g0081 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-34-2896C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614725 | ||||||
| chr4:73614783
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-34-2954G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614783 | ||||||
| chr4:73614817
|
A | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-34-2988T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614817 | ||||||
| chr4:73614997
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-34-3168A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73614997 | ||||||
| chr4:73615066
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34-3237G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615066 | ||||||
| chr4:73615117
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-34-3288A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615117 | ||||||
| chr4:73615125
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-34-3296C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615125 | ||||||
| chr4:73615178
|
C | CAA | 7 | a0001c0001t0001g0035a0001c0001t0001g0232a0001c0001t0007g0109others(4): Show | 8 | HG00609.hp1 HG02135.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-3351_-34-3350d others(4): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615178 | ||||||
| chr4:73615178
|
C | CAAA | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(192): Show | 240 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.-34-3352_-34-3350d others(5): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615178 | ||||||
| chr4:73615178
|
C | CAAAA | 67 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0152others(64): Show | 83 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-34-3353_-34-3350d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615178 | ||||||
| chr4:73615198
|
G | A | 2 | a0002c0002t0002g0069a0002c0002t0002g0072 | 2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-34-3369C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615198 | ||||||
| chr4:73615242
|
A | G | 1 | a0002c0002t0004g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-34-3413T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615242 | ||||||
| chr4:73615358
|
G | GTAGA | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-34-3533_-34-3530d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615358 | ||||||
| chr4:73615366
|
A | C | 1 | a0001c0001t0032g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-34-3537T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615366 | ||||||
| chr4:73615430
|
C | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-34-3601G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615430 | ||||||
| chr4:73615509
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-34-3680A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615509 | ||||||
| chr4:73615560
|
C | A | 14 | a0001c0001t0007g0021a0001c0001t0007g0109a0002c0002t0005g0022others(11): Show | 18 | HG01070.hp2 HG01071.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-34-3731G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615560 | ||||||
| chr4:73615562
|
A | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(36): Show | 50 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-34-3733T>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615562 | ||||||
| chr4:73615737
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-34-3908T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615737 | ||||||
| chr4:73615790
|
G | A | 1 | a0002c0002t0002g0082 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-34-3961C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73615790 | ||||||
| chr4:73616096
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0054 | 2 | HG00323.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-35+4192G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616096 | ||||||
| chr4:73616221
|
A | ATATC | 24 | a0001c0001t0001g0033a0001c0001t0001g0112a0001c0001t0001g0113others(21): Show | 25 | HG00639.hp1 HG00741.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-35+4063_-35+4066d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | ||||||
| chr4:73616221
|
A | ATATCTAT others(1): Show |
3 | a0001c0001t0001g0025a0001c0001t0001g0136a0001c0001t0031g0156 | 4 | HG03195.hp2 HG03927.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+4059_-35+4066d others(10): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | ||||||
| chr4:73616221
|
ATATC | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0030others(68): Show | 82 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-35+4063_-35+4066d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | ||||||
| chr4:73616221
|
ATATCTAT others(1): Show |
A | 13 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0036others(10): Show | 16 | HG00733.hp1 HG02071.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.-35+4059_-35+4066d others(10): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | ||||||
| chr4:73616221
|
ATATCTAT others(5): Show |
A | 1 | a0001c0001t0003g0198 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-35+4055_-35+4066d others(14): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616221 | ||||||
| chr4:73616247
|
A | G | 1 | a0002c0002t0004g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-35+4041T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616247 | ||||||
| chr4:73616600
|
T | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-35+3688A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616600 | ||||||
| chr4:73616668
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(36): Show | 50 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-35+3620G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616668 | ||||||
| chr4:73616679
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-35+3609C>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616679 | ||||||
| chr4:73616952
|
C | G | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-35+3336G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616952 | ||||||
| chr4:73616989
|
T | A | 1 | a0002c0002t0002g0091 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-35+3299A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73616989 | ||||||
| chr4:73617337
|
C | T | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-35+2951G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617337 | ||||||
| chr4:73617360
|
C | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(76): Show | 102 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-35+2928G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617360 | ||||||
| chr4:73617793
|
A | C | 1 | a0001c0001t0003g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-35+2495T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617793 | ||||||
| chr4:73617853
|
T | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-35+2435A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617853 | ||||||
| chr4:73617891
|
C | A | 3 | a0002c0002t0002g0026a0002c0002t0002g0181a0002c0002t0002g0199 | 4 | HG00140.hp1 HG01123.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+2397G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617891 | ||||||
| chr4:73617937
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-35+2351G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73617937 | ||||||
| chr4:73618022
|
T | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(36): Show | 50 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-35+2266A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618022 | ||||||
| chr4:73618252
|
G | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-35+2036C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618252 | ||||||
| chr4:73618300
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-35+1988C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618300 | ||||||
| chr4:73618301
|
T | TCTATCTA others(14): Show |
1 | a0001c0001t0001g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-35+1986_-35+1987i others(23): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618301
|
T | TTATC | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+1983_-35+1986d others(6): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618301
|
T | TTATCTAT others(1): Show |
17 | a0001c0001t0001g0030a0001c0001t0001g0209a0001c0001t0001g0210others(14): Show | 21 | HG01243.hp1 HG02027.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.-35+1979_-35+1986d others(10): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618301
|
T | TTATCTAT others(5): Show |
1 | a0002c0002t0002g0066 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-35+1975_-35+1986d others(14): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618301
|
T | TTATCTAT others(9): Show |
39 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(36): Show | 49 | HG00544.hp2 HG01070.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-35+1971_-35+1986d others(18): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618301
|
T | TTATCTAT others(13): Show |
99 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(96): Show | 120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-35+1967_-35+1986d others(22): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618301
|
T | TTATCTAT others(17): Show |
97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0014others(94): Show | 122 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.-35+1986_-35+1987i others(26): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618301
|
T | TTATCTAT others(21): Show |
16 | a0001c0001t0001g0038a0001c0001t0001g0149a0001c0001t0001g0150others(13): Show | 17 | HG00438.hp1 HG00741.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+1986_-35+1987i others(30): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618301
|
T | TTATCTAT others(25): Show |
2 | a0001c0001t0025g0267a0002c0002t0002g0108 | 2 | HG01952.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-35+1986_-35+1987i others(34): Show |
RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618301 | ||||||
| chr4:73618327
|
A | G | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+1961T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618327 | ||||||
| chr4:73618412
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG02572.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+1876G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618412 | ||||||
| chr4:73618629
|
C | T | 1 | a0001c0001t0018g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-35+1659G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618629 | ||||||
| chr4:73618927
|
C | G | 1 | a0001c0001t0029g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35+1361G>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618927 | ||||||
| chr4:73618971
|
T | C | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | NA18964.hp2 NA18971.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+1317A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618971 | ||||||
| chr4:73618982
|
A | C | 2 | a0001c0007t0014g0159a0001c0007t0014g0160 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-35+1306T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73618982 | ||||||
| chr4:73619066
|
C | A | 1 | a0001c0001t0029g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35+1222G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619066 | ||||||
| chr4:73619090
|
A | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-35+1198T>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619090 | ||||||
| chr4:73619108
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-35+1180A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619108 | ||||||
| chr4:73619131
|
A | G | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+1157T>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619131 | ||||||
| chr4:73619170
|
C | T | 1 | a0001c0001t0004g0203 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-35+1118G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619170 | ||||||
| chr4:73619255
|
T | G | 1 | a0001c0001t0003g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35+1033A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619255 | ||||||
| chr4:73619408
|
G | A | 3 | a0001c0001t0015g0157a0001c0001t0015g0158a0001c0001t0031g0156 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-35+880C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619408 | ||||||
| chr4:73619773
|
G | A | 2 | a0001c0007t0014g0159a0001c0007t0014g0160 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-35+515C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619773 | ||||||
| chr4:73619790
|
A | AT | 54 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(51): Show | 60 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-35+497dupA | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619790 | ||||||
| chr4:73619792
|
T | G | 2 | a0001c0007t0014g0159a0001c0007t0014g0160 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-35+496A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619792 | ||||||
| chr4:73619867
|
T | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-35+421A>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619867 | ||||||
| chr4:73619928
|
T | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.-35+360A>C | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619928 | ||||||
| chr4:73619947
|
G | A | 52 | a0002c0002t0001g0089a0002c0002t0001g0095a0002c0002t0002g0001others(49): Show | 66 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-35+341C>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73619947 | ||||||
| chr4:73620059
|
C | T | 2 | a0001c0001t0007g0021a0001c0001t0007g0109 | 3 | HG01070.hp2 HG01071.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+229G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620059 | ||||||
| chr4:73620151
|
C | T | 80 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(77): Show | 98 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-35+137G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620151 | ||||||
| chr4:73620179
|
C | A | 1 | a0001c0001t0001g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-35+109G>T | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620179 | ||||||
| chr4:73620197
|
T | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-35+91A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620197 | ||||||
| chr4:73620268
|
T | C | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(131): Show | 163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-35+20A>G | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620268 | ||||||
| chr4:73620278
|
C | T | 1 | a0001c0001t0003g0039 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-35+10G>A | RASSF6 | ENSG00000169435.14 | transcript | ENST00000307439.10 | protein_coding | 1/10 | chr4 | 73620278 |