Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 85021 |
|---|---|
| ensemblid | ENSG00000135597.19 |
| hgncid | 15578 |
| symbol | REPS1 |
| name | RALBP1 associated Eps domain containing 1 |
| refseq_nuc | NM_001286611.2 |
| refseq_prot | NP_001273540.1 |
| ensembl_nuc | ENST00000450536.7 |
| ensembl_prot | ENSP00000392065.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 138903493 |
| end | 138988253 |
| strand | - |
| ver | v1.2 |
| region | chr6:138903493-138988253 |
| region5000 | chr6:138898493-138993253 |
| regionname0 | REPS1_chr6_138903493_138988253 |
| regionname5000 | REPS1_chr6_138898493_138993253 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 796 | 348 | 73 | 54 | 172 | 12 | 35 | 143 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0002 | 0/0 | 796 | 28 | 14 | 3 | 10 | 0 | 1 | 8 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0003 | 0/0 | 796 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0004 | 0/0 | 796 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0005 | 0/0 | 796 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0006 | 0/0 | 796 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0007 | 0/0 | 796 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0008 | 0/0 | 796 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0009 | 0/0 | 796 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0010 | 0/0 | 796 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0011 | 0/0 | 796 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0012 | 0/0 | 796 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2391 | 266 | 46 | 52 | 122 | 12 | 32 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0002 | 0/0 | 2391 | 80 | 26 | 1 | 50 | 0 | 3 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0003 | 0/0 | 2391 | 28 | 14 | 3 | 10 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0004 | 0/0 | 2391 | 3 | 2 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0005 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0006 | 0/0 | 2391 | 2 | 1 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0007 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0008 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0009 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0010 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0011 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0012 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0013 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0014 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| c0015 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2143 | 189 | 34 | 29 | 98 | 5 | 22 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0002 | 0/1 | 2143 | 69 | 6 | 25 | 25 | 3 | 9 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0003 | 0/0 | 2131 | 64 | 26 | 2 | 34 | 0 | 2 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0004 | 0/0 | 2138 | 26 | 13 | 2 | 10 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0005 | 0/0 | 2137 | 5 | 0 | 0 | 5 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0006 | 0/0 | 2149 | 3 | 3 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0007 | 0/0 | 2143 | 3 | 0 | 1 | 0 | 2 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0008 | 0/0 | 2141 | 3 | 0 | 0 | 3 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0009 | 0/0 | 2143 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0010 | 0/0 | 2155 | 2 | 0 | 0 | 0 | 2 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0011 | 0/0 | 2141 | 2 | 0 | 0 | 1 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0012 | 0/0 | 2138 | 2 | 1 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0013 | 0/0 | 2143 | 2 | 0 | 0 | 2 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0014 | 0/0 | 2131 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0015 | 0/0 | 2131 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0016 | 0/0 | 2143 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0017 | 0/0 | 2155 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0018 | 0/0 | 2149 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0019 | 0/0 | 2149 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0020 | 0/0 | 2143 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0021 | 0/0 | 2143 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0022 | 0/0 | 2143 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0023 | 0/0 | 2143 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0024 | 0/0 | 2143 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0025 | 0/0 | 2143 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0026 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0027 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0028 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| t0029 | 0/0 | 2143 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2391 | 266 | 46 | 52 | 122 | 12 | 32 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002 | 0/0 | 2391 | 80 | 26 | 1 | 50 | 0 | 3 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0007 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0013 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0002c0003 | 0/0 | 2391 | 28 | 14 | 3 | 10 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0003c0004 | 0/0 | 2391 | 3 | 2 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0004c0006 | 0/0 | 2391 | 2 | 1 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0005c0005 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0006c0011 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0007c0009 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0008c0010 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0009c0008 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0010c0012 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0011c0014 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0012c0015 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4533 | 180 | 32 | 25 | 95 | 5 | 22 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0002 | 0/1 | 4533 | 59 | 6 | 24 | 16 | 3 | 9 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0003 | 0/0 | 4521 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0006 | 0/0 | 4539 | 3 | 3 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0007 | 0/0 | 4533 | 3 | 0 | 1 | 0 | 2 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0008 | 0/0 | 4531 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0009 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0010 | 0/0 | 4545 | 2 | 0 | 0 | 0 | 2 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0011 | 0/0 | 4531 | 2 | 0 | 0 | 1 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0013 | 0/0 | 4533 | 2 | 0 | 0 | 2 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0016 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0018 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0019 | 0/0 | 4539 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0020 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0021 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0022 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0023 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0024 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0025 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0026 | 0/0 | 4521 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0001t0029 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0002 | 0/0 | 4533 | 9 | 0 | 0 | 9 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0003 | 0/0 | 4521 | 58 | 21 | 1 | 34 | 0 | 2 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0005 | 0/0 | 4527 | 4 | 0 | 0 | 4 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0008 | 0/0 | 4531 | 2 | 0 | 0 | 2 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0014 | 0/0 | 4521 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0015 | 0/0 | 4521 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0017 | 0/0 | 4545 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0027 | 0/0 | 4521 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0002t0028 | 0/0 | 4521 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0007t0001 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0001c0013t0001 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0002c0003t0004 | 0/0 | 4528 | 26 | 13 | 2 | 10 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0002c0003t0012 | 0/0 | 4528 | 2 | 1 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0003c0004t0003 | 0/0 | 4521 | 3 | 2 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0004c0006t0001 | 0/0 | 4533 | 2 | 1 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0005c0005t0003 | 0/0 | 4521 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0006c0011t0001 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0007c0009t0001 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0008c0010t0001 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0009c0008t0001 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0010c0012t0002 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0011c0014t0001 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| a0012c0015t0005 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | copy fasta | chr6 | 138898493 | 138993253 |
| 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 | 2 | 1 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0011g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0013g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0013g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0016g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0018g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0019g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0020g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0021g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0022g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0023g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0024g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0025g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0026g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0001t0029g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0003g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0008g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0014g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0014g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0015g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0015g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0017g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0027g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0002t0028g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0007t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0001c0013t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0012g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0002c0003t0012g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0003c0004t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0003c0004t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0003c0004t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0004c0006t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0004c0006t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0005c0005t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0005c0005t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0006c0011t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0007c0009t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0008c0010t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0009c0008t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0010c0012t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0011c0014t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| a0012c0015t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0053 | EUR | FIN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0062 | EUR | FIN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0376 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0373 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00609 | hp2 | a0006 | c0011 | t0001 | g0298 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00621 | hp2 | a0001 | c0001 | t0029 | g0382 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00738 | hp2 | a0003 | c0004 | t0003 | g0316 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0359 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01069 | hp1 | a0002 | c0003 | t0012 | g0307 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01074 | hp2 | a0001 | c0001 | t0025 | g0217 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01081 | hp2 | a0001 | c0007 | t0001 | g0158 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01106 | hp1 | a0010 | c0012 | t0002 | g0061 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01192 | hp1 | a0002 | c0003 | t0004 | g0037 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01243 | hp2 | a0004 | c0006 | t0001 | g0290 | AMR | PUR | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0085 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01256 | hp2 | a0007 | c0009 | t0001 | g0303 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01346 | hp1 | a0009 | c0008 | t0001 | g0138 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01433 | hp2 | a0002 | c0003 | t0004 | g0040 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0008 | EUR | IBS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01516 | hp2 | a0001 | c0001 | t0010 | g0007 | EUR | IBS | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01884 | hp1 | a0002 | c0003 | t0012 | g0308 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0350 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02004 | hp1 | a0001 | c0001 | t0021 | g0015 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02015 | hp2 | a0002 | c0003 | t0004 | g0041 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0369 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0318 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02056 | hp1 | a0002 | c0003 | t0004 | g0030 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02129 | hp2 | a0001 | c0001 | t0011 | g0259 | EAS | KHV | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0379 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0335 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02165 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | CDX | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02165 | hp2 | a0001 | c0001 | t0016 | g0005 | EAS | CDX | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02257 | hp1 | a0002 | c0003 | t0004 | g0031 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0348 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02258 | hp2 | a0002 | c0003 | t0004 | g0017 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02451 | hp1 | a0002 | c0003 | t0004 | g0023 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0378 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02572 | hp1 | a0003 | c0004 | t0003 | g0317 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02572 | hp2 | a0002 | c0003 | t0004 | g0020 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0327 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02615 | hp2 | a0004 | c0006 | t0001 | g0134 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02622 | hp1 | a0002 | c0003 | t0004 | g0036 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02630 | hp1 | a0001 | c0002 | t0014 | g0385 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02647 | hp1 | a0003 | c0004 | t0003 | g0315 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02647 | hp2 | a0002 | c0003 | t0004 | g0024 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02717 | hp2 | a0001 | c0002 | t0015 | g0384 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02723 | hp2 | a0001 | c0002 | t0015 | g0383 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02809 | hp1 | a0002 | c0003 | t0004 | g0018 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0320 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02895 | hp1 | a0001 | c0002 | t0003 | g0352 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02895 | hp2 | a0005 | c0005 | t0003 | g0323 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02896 | hp1 | a0005 | c0005 | t0003 | g0322 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0353 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0099 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0347 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0326 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0325 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0319 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02976 | hp1 | a0001 | c0002 | t0028 | g0351 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0330 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03486 | hp1 | a0001 | c0002 | t0014 | g0386 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0329 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03516 | hp1 | a0001 | c0013 | t0001 | g0130 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03516 | hp2 | a0002 | c0003 | t0004 | g0038 | AFR | ESN | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0349 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03540 | hp2 | a0002 | c0003 | t0004 | g0019 | AFR | GWD | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0161 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0375 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03704 | hp2 | a0001 | c0002 | t0017 | g0006 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03831 | hp2 | a0002 | c0003 | t0004 | g0027 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0332 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0361 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0216 | SAS | STU | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | STU | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0374 | AFR | YRI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0370 | EAS | CHB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | YRI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0328 | AFR | YRI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18940 | hp2 | a0001 | c0002 | t0008 | g0119 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18941 | hp2 | a0001 | c0001 | t0018 | g0012 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0362 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0340 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18948 | hp1 | a0001 | c0001 | t0020 | g0014 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18949 | hp2 | a0012 | c0015 | t0005 | g0314 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0339 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18956 | hp1 | a0002 | c0003 | t0004 | g0029 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18957 | hp2 | a0002 | c0003 | t0004 | g0026 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0366 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18964 | hp1 | a0001 | c0001 | t0024 | g0262 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18965 | hp2 | a0001 | c0001 | t0026 | g0306 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18966 | hp1 | a0002 | c0003 | t0004 | g0032 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18968 | hp2 | a0002 | c0003 | t0004 | g0033 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0377 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18970 | hp1 | a0001 | c0001 | t0013 | g0380 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18970 | hp2 | a0001 | c0002 | t0005 | g0313 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18974 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0371 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0365 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18979 | hp2 | a0011 | c0014 | t0001 | g0271 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0338 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0337 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18982 | hp2 | a0001 | c0002 | t0005 | g0312 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0357 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0342 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0363 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18989 | hp1 | a0001 | c0002 | t0008 | g0117 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18989 | hp2 | a0001 | c0002 | t0027 | g0309 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0333 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0311 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0372 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0358 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19005 | hp1 | a0001 | c0002 | t0003 | g0356 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19005 | hp2 | a0002 | c0003 | t0004 | g0039 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0331 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0346 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19011 | hp2 | a0001 | c0002 | t0003 | g0364 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19012 | hp1 | a0001 | c0002 | t0003 | g0360 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19043 | hp1 | a0002 | c0003 | t0004 | g0021 | AFR | LWK | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19056 | hp1 | a0002 | c0003 | t0004 | g0034 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19056 | hp2 | a0001 | c0001 | t0019 | g0013 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19057 | hp1 | a0001 | c0002 | t0003 | g0367 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0354 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0334 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0355 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19070 | hp2 | a0002 | c0003 | t0004 | g0028 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0336 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19080 | hp1 | a0001 | c0001 | t0013 | g0381 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19081 | hp1 | a0001 | c0002 | t0005 | g0310 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19082 | hp1 | a0001 | c0002 | t0003 | g0368 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19082 | hp2 | a0002 | c0003 | t0004 | g0035 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19084 | hp2 | a0008 | c0010 | t0001 | g0171 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0344 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0321 | AFR | YRI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | YRI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0050 | EUR | TSI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | TSI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0105 | EUR | TSI | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | GIH | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0025 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02559 | hp1 | a0002 | c0003 | t0004 | g0016 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | USA | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| HG06807 | hp2 | a0002 | c0003 | t0004 | g0022 | AFR | USA | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0341 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | USA | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA20300 | hp2 | a0001 | c0001 | t0023 | g0098 | AFR | USA | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | LWK | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | LWK | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0051 | REF | REF | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | REPS1_chr6_138898493_138993253 | REPS1 | chr6 | 138898493 | 138993253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:138908735
|
C | T | 1 | a0002 | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
missense_variant | MODERATE | c.2149G>A | p.Val717Ile | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/20 | 2720/4533 | 2149/2391 | 717/796 | chr6 | 138908735 | ||
| chr6:138911287
|
G | A | 1 | a0007 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.2056C>T | p.Pro686Ser | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/20 | 2627/4533 | 2056/2391 | 686/796 | chr6 | 138911287 | ||
| chr6:138911306
|
T | G | 1 | a0005 | 2 | HG02895.hp2 HG02896.hp1 |
missense_variant | MODERATE | c.2037A>C | p.Glu679Asp | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/20 | 2608/4533 | 2037/2391 | 679/796 | chr6 | 138911306 | ||
| chr6:138912766
|
G | A | 1 | a0004 | 2 | HG01243.hp2 HG02615.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1970C>T | p.Pro657Leu | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/20 | 2541/4533 | 1970/2391 | 657/796 | chr6 | 138912766 | ||
| chr6:138912775
|
T | C | 1 | a0008 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.1961A>G | p.Glu654Gly | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/20 | 2532/4533 | 1961/2391 | 654/796 | chr6 | 138912775 | ||
| chr6:138912809
|
C | T | 1 | a0009 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1927G>A | p.Asp643Asn | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/20 | 2498/4533 | 1927/2391 | 643/796 | chr6 | 138912809 | ||
| chr6:138912893
|
T | C | 1 | a0006 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1843A>G | p.Ser615Gly | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/20 | 2414/4533 | 1843/2391 | 615/796 | chr6 | 138912893 | ||
| chr6:138912905
|
T | C | 1 | a0010 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1831A>G | p.Ile611Val | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/20 | 2402/4533 | 1831/2391 | 611/796 | chr6 | 138912905 | ||
| chr6:138912947
|
G | A | 1 | a0003 | 3 | HG00738.hp2 HG02572.hp1 HG02647.hp1 |
missense_variant | MODERATE | c.1789C>T | p.Pro597Ser | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/20 | 2360/4533 | 1789/2391 | 597/796 | chr6 | 138912947 | ||
| chr6:138944514
|
T | C | 1 | a0011 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.737A>G | p.His246Arg | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 5/20 | 1308/4533 | 737/2391 | 246/796 | chr6 | 138944514 | ||
| chr6:138987651
|
T | C | 1 | a0012 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.32A>G | p.Gln11Arg | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 603/4533 | 32/2391 | 11/796 | chr6 | 138987651 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:138920234
|
G | A | 1 | a0001c0013 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1509C>T | p.Phe503Phe | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/20 | 2080/4533 | 1509/2391 | 503/796 | chr6 | 138920234 | ||
| chr6:138945265
|
G | A | 3 | a0001c0002a0003c0004a0012c0015 | 84 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(81): Show |
synonymous_variant | LOW | c.582C>T | p.Leu194Leu | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 4/20 | 1153/4533 | 582/2391 | 194/796 | chr6 | 138945265 | ||
| chr6:138945531
|
C | T | 1 | a0001c0007 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.444G>A | p.Thr148Thr | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 3/20 | 1015/4533 | 444/2391 | 148/796 | chr6 | 138945531 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:138903510
|
G | A | 1 | a0001c0002t0028 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1554C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 1554 | chr6 | 138903510 | |||||
| chr6:138903549
|
C | A | 20 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(17): Show | 154 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1515G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 1515 | chr6 | 138903549 | |||||
| chr6:138903608
|
C | T | 1 | a0001c0001t0022 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1456G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 1456 | chr6 | 138903608 | |||||
| chr6:138903766
|
A | G | 2 | a0002c0003t0004a0002c0003t0012 | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1298T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 1298 | chr6 | 138903766 | |||||
| chr6:138903925
|
T | C | 1 | a0001c0002t0015 | 2 | HG02717.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 1139 | chr6 | 138903925 | |||||
| chr6:138904036
|
T | C | 1 | a0001c0001t0024 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1028A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 1028 | chr6 | 138904036 | |||||
| chr6:138904420
|
T | C | 1 | a0001c0001t0025 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 644 | chr6 | 138904420 | |||||
| chr6:138904493
|
CAT | C | 3 | a0001c0001t0008a0001c0001t0011a0001c0002t0008 | 5 | HG02129.hp2 HG02165.hp1 HG04115.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*569_*570delAT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 569 | chr6 | 138904493 | |||||
| chr6:138904654
|
A | G | 1 | a0001c0001t0007 | 3 | HG00280.hp1 HG00323.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 410 | chr6 | 138904654 | |||||
| chr6:138904663
|
TATAGA | T | 2 | a0002c0003t0004a0002c0003t0012 | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*396_*400delTCTAT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 396 | chr6 | 138904663 | |||||
| chr6:138904788
|
G | T | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(20): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*276C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 276 | chr6 | 138904788 | |||||
| chr6:138904800
|
T | C | 2 | a0001c0002t0014a0001c0002t0015 | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*264A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 20/20 | 264 | chr6 | 138904800 | |||||
| chr6:138987776
|
C | T | 1 | a0001c0001t0021 | 1 | HG02004.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 94 | chr6 | 138987776 | |||||
| chr6:138987841
|
G | A | 2 | a0001c0002t0014a0001c0002t0015 | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-159C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | chr6 | 138987841 | ||||||
| chr6:138987901
|
C | T | 1 | a0001c0001t0020 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-219G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 219 | chr6 | 138987901 | |||||
| chr6:138987915
|
C | G | 10 | a0001c0001t0003a0001c0002t0003a0001c0002t0005others(7): Show | 75 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(72): Show |
5_prime_UTR_variant | MODIFIER | c.-233G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 233 | chr6 | 138987915 | |||||
| chr6:138987932
|
A | ACGGCTC | 3 | a0001c0001t0006a0001c0001t0018a0001c0001t0019 | 5 | HG02717.hp1 HG03139.hp2 HG03453.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-256_-251dupGAGCCG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 251 | chr6 | 138987932 | |||||
| chr6:138987932
|
A | ACGGCTCC others(5): Show |
2 | a0001c0001t0010a0001c0002t0017 | 3 | HG01515.hp1 HG01516.hp2 HG03704.hp2 |
5_prime_UTR_variant | MODIFIER | c.-262_-251dupGAGCCG others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 251 | chr6 | 138987932 | |||||
| chr6:138987932
|
ACGGCTC | A | 2 | a0001c0002t0005a0012c0015t0005 | 5 | NA18949.hp2 NA18970.hp2 NA18982.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-256_-251delGAGCCG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 251 | chr6 | 138987932 | |||||
| chr6:138987932
|
ACGGCTCC others(5): Show |
A | 9 | a0001c0001t0003a0001c0001t0026a0001c0002t0003others(6): Show | 71 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(68): Show |
5_prime_UTR_variant | MODIFIER | c.-262_-251delGAGCCG others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 251 | chr6 | 138987932 | |||||
| chr6:138988026
|
C | T | 1 | a0001c0002t0027 | 1 | NA18989.hp2 | 5_prime_UTR_variant | MODIFIER | c.-344G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 344 | chr6 | 138988026 | |||||
| chr6:138988031
|
G | A | 1 | a0002c0003t0012 | 2 | HG01069.hp1 HG01884.hp1 |
5_prime_UTR_variant | MODIFIER | c.-349C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 349 | chr6 | 138988031 | |||||
| chr6:138988034
|
G | A | 8 | a0001c0001t0003a0001c0002t0003a0001c0002t0005others(5): Show | 71 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(68): Show |
5_prime_UTR_variant | MODIFIER | c.-352C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 352 | chr6 | 138988034 | |||||
| chr6:138988132
|
T | C | 1 | a0001c0001t0013 | 2 | NA18970.hp1 NA19080.hp1 |
5_prime_UTR_variant | MODIFIER | c.-450A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 450 | chr6 | 138988132 | |||||
| chr6:138988181
|
C | A | 1 | a0001c0001t0029 | 1 | HG00621.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-499G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | chr6 | 138988181 | ||||||
| chr6:138988224
|
C | T | 1 | a0001c0001t0016 | 1 | HG02165.hp2 | 5_prime_UTR_variant | MODIFIER | c.-542G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 542 | chr6 | 138988224 | |||||
| chr6:138988240
|
G | A | 2 | a0001c0002t0014a0001c0002t0015 | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-558C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 558 | chr6 | 138988240 | |||||
| chr6:138988253
|
C | T | 1 | a0001c0001t0009 | 2 | HG03579.hp1 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-571G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/20 | 571 | chr6 | 138988253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:138905352
|
C | A | 4 | a0001c0002t0003g0325a0001c0002t0003g0352a0001c0002t0003g0353others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2323-220G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905352 | ||||||
| chr6:138905352
|
C | T | 18 | a0002c0003t0004g0026a0002c0003t0004g0027a0002c0003t0004g0028others(15): Show | 18 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.2323-220G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905352 | ||||||
| chr6:138905384
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2323-252G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905384 | ||||||
| chr6:138905457
|
A | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0220 | 2 | NA19063.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2323-325T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905457 | ||||||
| chr6:138905493
|
T | G | 158 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(155): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.2323-361A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905493 | ||||||
| chr6:138905495
|
G | T | 158 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(155): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.2323-363C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905495 | ||||||
| chr6:138905502
|
A | G | 158 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(155): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.2323-370T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905502 | ||||||
| chr6:138905580
|
CG | C | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.2323-449delC | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905580 | ||||||
| chr6:138905582
|
C | T | 158 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(155): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.2323-450G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905582 | ||||||
| chr6:138905601
|
C | T | 158 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(155): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.2323-469G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905601 | ||||||
| chr6:138905752
|
CT | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2323-621delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905752 | ||||||
| chr6:138905846
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02074.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2323-714T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905846 | ||||||
| chr6:138905885
|
T | C | 2 | a0001c0001t0001g0139a0009c0008t0001g0138 | 2 | HG00639.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2323-753A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905885 | ||||||
| chr6:138905962
|
T | C | 67 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(64): Show | 67 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.2323-830A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138905962 | ||||||
| chr6:138906064
|
T | C | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.2323-932A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906064 | ||||||
| chr6:138906167
|
C | T | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2323-1035G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906167 | ||||||
| chr6:138906248
|
G | A | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 314 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(311): Show |
intron_variant | MODIFIER | c.2323-1116C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906248 | ||||||
| chr6:138906342
|
A | C | 187 | a0001c0001t0001g0110a0001c0001t0002g0042a0001c0001t0002g0043others(184): Show | 188 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.2322+1153T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906342 | ||||||
| chr6:138906351
|
A | G | 3 | a0001c0002t0003g0347a0001c0002t0003g0348a0001c0002t0003g0350 | 3 | HG01891.hp1 HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2322+1144T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906351 | ||||||
| chr6:138906393
|
T | G | 73 | a0001c0001t0001g0110a0001c0001t0002g0042a0001c0001t0002g0043others(70): Show | 73 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.2322+1102A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906393 | ||||||
| chr6:138906438
|
G | A | 158 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(155): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.2322+1057C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906438 | ||||||
| chr6:138906480
|
G | A | 79 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(76): Show | 80 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.2322+1015C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906480 | ||||||
| chr6:138906498
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2322+997G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906498 | ||||||
| chr6:138906566
|
C | T | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2322+929G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906566 | ||||||
| chr6:138906669
|
T | C | 21 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(18): Show | 21 | HG00639.hp1 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2322+826A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138906669 | ||||||
| chr6:138907129
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2322+366T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907129 | ||||||
| chr6:138907297
|
T | TA | 6 | a0001c0002t0003g0325a0001c0002t0003g0331a0001c0002t0003g0354others(3): Show | 6 | HG02965.hp2 HG03704.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.2322+197dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907297 | ||||||
| chr6:138907312
|
AAGT | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0173a0001c0001t0001g0178others(3): Show | 6 | HG01074.hp2 HG01516.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2322+180_2322+182d others(5): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907312 | ||||||
| chr6:138907313
|
A | AAGTGTGT others(4): Show |
2 | a0001c0001t0002g0060a0002c0003t0004g0018 | 2 | HG00738.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2322+181_2322+182i others(13): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AAGTGTGT others(6): Show |
56 | a0001c0001t0002g0044a0001c0001t0002g0046a0001c0001t0002g0047others(53): Show | 56 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.2322+181_2322+182i others(15): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AAGTGTGT others(8): Show |
17 | a0001c0001t0002g0050a0001c0001t0002g0066a0001c0001t0002g0070others(14): Show | 17 | HG00741.hp2 HG01515.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.2322+181_2322+182i others(17): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AAGTGTGT others(10): Show |
9 | a0001c0001t0002g0075a0001c0001t0002g0100a0002c0003t0004g0019others(6): Show | 9 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2322+181_2322+182i others(19): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AAGTGTGT others(12): Show |
3 | a0001c0001t0002g0042a0001c0001t0002g0076a0002c0003t0004g0020 | 3 | HG01081.hp1 HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2322+181_2322+182i others(21): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AAGTGTGT others(14): Show |
1 | a0001c0001t0007g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2322+181_2322+182i others(23): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AAGTGTGT others(16): Show |
2 | a0001c0001t0021g0015a0002c0003t0004g0036 | 2 | HG02004.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2322+181_2322+182i others(25): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AATGTGTG others(7): Show |
1 | a0001c0001t0002g0092 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2322+181_2322+182i others(16): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AGT | 7 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG00597.hp1 HG02735.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.2322+180_2322+181d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AGTGTGTG others(5): Show |
3 | a0001c0001t0007g0062a0001c0001t0020g0014a0002c0003t0004g0041 | 3 | HG00323.hp1 HG02015.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.2322+170_2322+181d others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
A | AGTGTGTG others(9): Show |
1 | a0002c0003t0004g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2322+166_2322+181d others(18): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
AG | A | 70 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(67): Show | 71 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.2322+181delC | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
AGT | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 114 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.2322+180_2322+181d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907313
|
AGTG | A | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2322+179_2322+181d others(5): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907313 | ||||||
| chr6:138907315
|
T | A | 70 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(67): Show | 71 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.2322+180A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907315 | ||||||
| chr6:138907317
|
T | A | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2322+178A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907317 | ||||||
| chr6:138907376
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2322+119A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907376 | ||||||
| chr6:138907446
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2322+49A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907446 | ||||||
| chr6:138907479
|
T | A | 1 | a0010c0012t0002g0061 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2322+16A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907479 | ||||||
| chr6:138907480
|
C | T | 1 | a0010c0012t0002g0061 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2322+15G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 19/19 | chr6 | 138907480 | ||||||
| chr6:138907741
|
C | T | 7 | a0001c0002t0003g0336a0001c0002t0003g0343a0001c0002t0003g0344others(4): Show | 7 | NA18939.hp1 NA18974.hp1 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.2217-141G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138907741 | ||||||
| chr6:138907895
|
T | C | 4 | a0001c0002t0003g0325a0001c0002t0003g0352a0001c0002t0003g0353others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217-295A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138907895 | ||||||
| chr6:138908055
|
C | A | 1 | a0001c0001t0001g0272 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2217-455G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908055 | ||||||
| chr6:138908055
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2217-455G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908055 | ||||||
| chr6:138908075
|
T | C | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217-475A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908075 | ||||||
| chr6:138908225
|
A | AC | 85 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(82): Show | 86 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.2216+442dupG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908225 | ||||||
| chr6:138908267
|
G | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2216+401C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908267 | ||||||
| chr6:138908360
|
C | T | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.2216+308G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908360 | ||||||
| chr6:138908419
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2216+249G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908419 | ||||||
| chr6:138908456
|
G | A | 1 | a0001c0002t0014g0386 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2216+212C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908456 | ||||||
| chr6:138908492
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2216+176A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908492 | ||||||
| chr6:138908558
|
A | G | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 299 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(296): Show |
intron_variant | MODIFIER | c.2216+110T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908558 | ||||||
| chr6:138908606
|
C | T | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(303): Show | 310 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(307): Show |
intron_variant | MODIFIER | c.2216+62G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908606 | ||||||
| chr6:138908618
|
G | A | 2 | a0001c0001t0022g0099a0001c0001t0023g0098 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2216+50C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 18/19 | chr6 | 138908618 | ||||||
| chr6:138908823
|
G | A | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2068-7C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138908823 | ||||||
| chr6:138908950
|
T | C | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2068-134A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138908950 | ||||||
| chr6:138909053
|
A | T | 1 | a0001c0002t0005g0312 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2068-237T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909053 | ||||||
| chr6:138909207
|
G | A | 190 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(187): Show | 191 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.2068-391C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909207 | ||||||
| chr6:138909286
|
A | T | 153 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(150): Show | 154 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.2068-470T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909286 | ||||||
| chr6:138909368
|
G | A | 4 | a0002c0003t0004g0032a0002c0003t0004g0033a0002c0003t0004g0034others(1): Show | 4 | NA18966.hp1 NA18968.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068-552C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909368 | ||||||
| chr6:138909458
|
C | G | 1 | a0002c0003t0004g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2068-642G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909458 | ||||||
| chr6:138909523
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2068-707A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909523 | ||||||
| chr6:138909542
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(10): Show | 14 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2068-726C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909542 | ||||||
| chr6:138909548
|
C | T | 60 | a0001c0002t0003g0318a0001c0002t0003g0319a0001c0002t0003g0320others(57): Show | 60 | HG00423.hp2 HG00438.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.2068-732G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909548 | ||||||
| chr6:138909552
|
G | T | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.2068-736C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909552 | ||||||
| chr6:138909740
|
G | A | 67 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(64): Show | 67 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.2068-924C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909740 | ||||||
| chr6:138909802
|
CTT | C | 153 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(150): Show | 154 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.2068-988_2068-987d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909802 | ||||||
| chr6:138909817
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2068-1001A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909817 | ||||||
| chr6:138909832
|
T | C | 66 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.2068-1016A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138909832 | ||||||
| chr6:138910030
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2068-1214A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910030 | ||||||
| chr6:138910033
|
T | C | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2068-1217A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910033 | ||||||
| chr6:138910395
|
C | A | 62 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(59): Show | 62 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2067+881G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910395 | ||||||
| chr6:138910432
|
C | T | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2067+844G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910432 | ||||||
| chr6:138910439
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.2067+837G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910439 | ||||||
| chr6:138910465
|
C | A | 1 | a0001c0007t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2067+811G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910465 | ||||||
| chr6:138910499
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.2067+777C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910499 | ||||||
| chr6:138910500
|
C | T | 1 | a0001c0001t0002g0075 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2067+776G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910500 | ||||||
| chr6:138910597
|
G | A | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.2067+679C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910597 | ||||||
| chr6:138910733
|
A | G | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2067+543T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910733 | ||||||
| chr6:138910800
|
T | C | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2067+476A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910800 | ||||||
| chr6:138910866
|
A | T | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2067+410T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910866 | ||||||
| chr6:138910905
|
C | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.2067+371G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138910905 | ||||||
| chr6:138911002
|
G | T | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2067+274C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 17/19 | chr6 | 138911002 | ||||||
| chr6:138911442
|
C | A | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.1972-71G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138911442 | ||||||
| chr6:138911572
|
G | A | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1972-201C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138911572 | ||||||
| chr6:138911653
|
CAGATGTG others(36): Show |
C | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1972-325_1972-283d others(45): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138911653 | ||||||
| chr6:138911715
|
A | G | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972-344T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138911715 | ||||||
| chr6:138911838
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1972-467C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138911838 | ||||||
| chr6:138912123
|
A | G | 26 | a0001c0001t0001g0276a0002c0003t0004g0019a0002c0003t0004g0020others(23): Show | 26 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.1971+642T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138912123 | ||||||
| chr6:138912158
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1971+607G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138912158 | ||||||
| chr6:138912216
|
T | A | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1971+549A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138912216 | ||||||
| chr6:138912426
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1971+339C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138912426 | ||||||
| chr6:138912468
|
A | G | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1971+297T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138912468 | ||||||
| chr6:138912488
|
T | C | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1971+277A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138912488 | ||||||
| chr6:138912730
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1971+35G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 16/19 | chr6 | 138912730 | ||||||
| chr6:138912957
|
A | G | 1 | a0001c0002t0003g0375 | 1 | HG03579.hp2 | splice_region_variant&intron_variant | LOW | c.1786-7T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138912957 | ||||||
| chr6:138913026
|
C | T | 185 | a0001c0001t0001g0110a0001c0001t0002g0042a0001c0001t0002g0043others(182): Show | 186 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1786-76G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913026 | ||||||
| chr6:138913093
|
C | G | 22 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(19): Show | 23 | HG00738.hp2 HG02027.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1786-143G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913093 | ||||||
| chr6:138913111
|
T | C | 1 | a0001c0002t0003g0343 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1786-161A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913111 | ||||||
| chr6:138913141
|
C | G | 1 | a0001c0001t0022g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1786-191G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913141 | ||||||
| chr6:138913218
|
A | C | 187 | a0001c0001t0001g0110a0001c0001t0002g0042a0001c0001t0002g0043others(184): Show | 188 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.1786-268T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913218 | ||||||
| chr6:138913407
|
C | T | 73 | a0001c0001t0001g0110a0001c0001t0002g0042a0001c0001t0002g0043others(70): Show | 73 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1786-457G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913407 | ||||||
| chr6:138913491
|
G | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 298 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(295): Show |
intron_variant | MODIFIER | c.1786-541C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913491 | ||||||
| chr6:138913554
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1786-604C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913554 | ||||||
| chr6:138913670
|
C | T | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1786-720G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913670 | ||||||
| chr6:138913728
|
A | T | 1 | a0001c0002t0003g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1786-778T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913728 | ||||||
| chr6:138913809
|
G | C | 1 | a0002c0003t0004g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1786-859C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138913809 | ||||||
| chr6:138914084
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1785+613A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138914084 | ||||||
| chr6:138914118
|
G | GC | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1785+578_1785+579i others(3): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138914118 | ||||||
| chr6:138914216
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1785+481G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138914216 | ||||||
| chr6:138914239
|
T | TTTTTG | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1785+453_1785+457d others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138914239 | ||||||
| chr6:138914500
|
G | A | 79 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(76): Show | 80 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1785+197C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 15/19 | chr6 | 138914500 | ||||||
| chr6:138914783
|
T | C | 2 | a0001c0001t0001g0297a0001c0001t0001g0299 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1721-22A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 14/19 | chr6 | 138914783 | ||||||
| chr6:138914921
|
C | T | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1721-160G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 14/19 | chr6 | 138914921 | ||||||
| chr6:138915179
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1721-418A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 14/19 | chr6 | 138915179 | ||||||
| chr6:138915373
|
A | C | 1 | a0001c0001t0001g0002 | 2 | HG01106.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1720+485T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 14/19 | chr6 | 138915373 | ||||||
| chr6:138915452
|
A | AT | 9 | a0001c0001t0001g0236a0001c0001t0001g0248a0001c0001t0001g0280others(6): Show | 9 | HG00738.hp2 HG02027.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+405dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 14/19 | chr6 | 138915452 | ||||||
| chr6:138915452
|
AT | A | 100 | a0001c0001t0001g0187a0001c0001t0001g0212a0001c0001t0002g0042others(97): Show | 100 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1720+405delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 14/19 | chr6 | 138915452 | ||||||
| chr6:138915624
|
T | C | 1 | a0002c0003t0012g0307 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1720+234A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 14/19 | chr6 | 138915624 | ||||||
| chr6:138915673
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1720+185C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 14/19 | chr6 | 138915673 | ||||||
| chr6:138916218
|
C | CT | 12 | a0001c0001t0001g0159a0001c0001t0001g0175a0001c0001t0001g0248others(9): Show | 12 | HG00733.hp2 HG00741.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1602-243dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916218 | ||||||
| chr6:138916218
|
CT | C | 16 | a0001c0001t0001g0132a0001c0001t0001g0144a0001c0001t0001g0145others(13): Show | 16 | HG01074.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602-243delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916218 | ||||||
| chr6:138916218
|
CTT | C | 31 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(28): Show | 31 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602-244_1602-243d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916218 | ||||||
| chr6:138916218
|
CTTTT | C | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.1602-246_1602-243d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916218 | ||||||
| chr6:138916218
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0003g0344 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1602-253_1602-243d others(13): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916218 | ||||||
| chr6:138916218
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1602-254_1602-243d others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916218 | ||||||
| chr6:138916224
|
T | C | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-248A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916224 | ||||||
| chr6:138916226
|
T | C | 8 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602-250A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916226 | ||||||
| chr6:138916307
|
G | A | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1602-331C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916307 | ||||||
| chr6:138916421
|
A | ATGT | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602-448_1602-446d others(5): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916421 | ||||||
| chr6:138916476
|
C | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1602-500G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916476 | ||||||
| chr6:138916507
|
G | A | 158 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(155): Show | 159 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1602-531C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916507 | ||||||
| chr6:138916669
|
A | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1602-693T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916669 | ||||||
| chr6:138916822
|
C | A | 190 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(187): Show | 191 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.1601+733G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916822 | ||||||
| chr6:138916917
|
G | C | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1601+638C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916917 | ||||||
| chr6:138916979
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1601+576G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138916979 | ||||||
| chr6:138917058
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1601+497T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138917058 | ||||||
| chr6:138917061
|
G | C | 66 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1601+494C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138917061 | ||||||
| chr6:138917072
|
A | G | 3 | a0002c0003t0004g0036a0002c0003t0004g0038a0002c0003t0004g0040 | 3 | HG01433.hp2 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1601+483T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138917072 | ||||||
| chr6:138917179
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1601+376C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138917179 | ||||||
| chr6:138917462
|
G | T | 79 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(76): Show | 80 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.1601+93C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 13/19 | chr6 | 138917462 | ||||||
| chr6:138917802
|
T | G | 1 | a0004c0006t0001g0290 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1529-175A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138917802 | ||||||
| chr6:138917860
|
C | T | 2 | a0001c0002t0003g0321a0001c0002t0003g0374 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1529-233G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138917860 | ||||||
| chr6:138917902
|
C | G | 1 | a0001c0002t0003g0319 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1529-275G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138917902 | ||||||
| chr6:138918050
|
C | T | 1 | a0001c0001t0003g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1529-423G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918050 | ||||||
| chr6:138918089
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1529-462T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918089 | ||||||
| chr6:138918093
|
T | TTG | 27 | a0002c0003t0004g0019a0002c0003t0004g0020a0002c0003t0004g0021others(24): Show | 27 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1529-468_1529-467d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918093 | ||||||
| chr6:138918093
|
T | TTGTG | 3 | a0001c0001t0003g0324a0002c0003t0004g0017a0002c0003t0004g0018 | 3 | HG02258.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1529-470_1529-467d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918093 | ||||||
| chr6:138918240
|
C | T | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1529-613G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918240 | ||||||
| chr6:138918605
|
T | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1529-978A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918605 | ||||||
| chr6:138918614
|
C | G | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.1529-987G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918614 | ||||||
| chr6:138918732
|
T | C | 187 | a0001c0001t0001g0110a0001c0001t0002g0042a0001c0001t0002g0043others(184): Show | 188 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.1529-1105A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918732 | ||||||
| chr6:138918760
|
C | A | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1529-1133G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918760 | ||||||
| chr6:138918836
|
T | C | 4 | a0001c0002t0005g0310a0001c0002t0005g0311a0001c0002t0005g0312others(1): Show | 4 | NA18949.hp2 NA18982.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1529-1209A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918836 | ||||||
| chr6:138918880
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1529-1253C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918880 | ||||||
| chr6:138918958
|
A | G | 5 | a0001c0001t0001g0264a0001c0001t0001g0274a0001c0001t0001g0286others(2): Show | 5 | HG02129.hp2 NA18979.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1528+1257T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138918958 | ||||||
| chr6:138919029
|
A | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0224 | 2 | HG01109.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1528+1186T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919029 | ||||||
| chr6:138919241
|
T | C | 73 | a0001c0001t0001g0110a0001c0001t0002g0042a0001c0001t0002g0043others(70): Show | 73 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1528+974A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919241 | ||||||
| chr6:138919247
|
A | G | 77 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(74): Show | 78 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1528+968T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919247 | ||||||
| chr6:138919384
|
T | C | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1528+831A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919384 | ||||||
| chr6:138919423
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1528+792C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919423 | ||||||
| chr6:138919523
|
C | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02735.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1528+692G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919523 | ||||||
| chr6:138919547
|
T | A | 1 | a0001c0001t0001g0276 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1528+668A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919547 | ||||||
| chr6:138919773
|
G | A | 1 | a0001c0001t0009g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1528+442C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919773 | ||||||
| chr6:138919830
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1528+385T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919830 | ||||||
| chr6:138919860
|
T | TAA | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1528+354_1528+355i others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919860 | ||||||
| chr6:138919861
|
T | A | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1528+354A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138919861 | ||||||
| chr6:138920056
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1528+159C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138920056 | ||||||
| chr6:138920089
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1528+126G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138920089 | ||||||
| chr6:138920195
|
A | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1528+20T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 12/19 | chr6 | 138920195 | ||||||
| chr6:138920394
|
C | T | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1427-78G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 11/19 | chr6 | 138920394 | ||||||
| chr6:138920551
|
C | T | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1427-235G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 11/19 | chr6 | 138920551 | ||||||
| chr6:138921166
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1339-42C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921166 | ||||||
| chr6:138921331
|
T | TA | 8 | a0001c0001t0001g0126a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 8 | HG00733.hp1 HG00741.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1339-208dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921331 | ||||||
| chr6:138921331
|
TA | T | 8 | a0001c0001t0020g0014a0001c0001t0022g0099a0001c0001t0023g0098others(5): Show | 8 | HG01081.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1339-208delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921331 | ||||||
| chr6:138921391
|
C | G | 190 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(187): Show | 191 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.1339-267G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921391 | ||||||
| chr6:138921399
|
C | T | 1 | a0001c0002t0002g0123 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1339-275G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921399 | ||||||
| chr6:138921470
|
T | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-346A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921470 | ||||||
| chr6:138921529
|
T | C | 3 | a0002c0003t0004g0036a0002c0003t0004g0038a0002c0003t0004g0040 | 3 | HG01433.hp2 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1339-405A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921529 | ||||||
| chr6:138921543
|
C | T | 2 | a0001c0002t0003g0338a0001c0002t0003g0342 | 2 | NA18980.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1339-419G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921543 | ||||||
| chr6:138921567
|
C | CT | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0128others(99): Show | 104 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.1339-444dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921567 | ||||||
| chr6:138921567
|
C | CTT | 19 | a0001c0001t0001g0140a0001c0001t0001g0163a0001c0001t0001g0168others(16): Show | 19 | HG00544.hp1 HG00597.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1339-445_1339-444d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921567 | ||||||
| chr6:138921567
|
CT | C | 140 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0270others(137): Show | 140 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1339-444delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921567 | ||||||
| chr6:138921567
|
CTT | C | 24 | a0001c0001t0002g0096a0001c0002t0002g0001a0001c0002t0002g0116others(21): Show | 25 | HG00738.hp2 HG02027.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1339-445_1339-444d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921567 | ||||||
| chr6:138921704
|
A | C | 1 | a0001c0002t0003g0325 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1339-580T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921704 | ||||||
| chr6:138921709
|
C | T | 7 | a0002c0003t0004g0019a0002c0003t0004g0020a0002c0003t0004g0021others(4): Show | 7 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1339-585G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921709 | ||||||
| chr6:138921895
|
C | G | 1 | a0001c0001t0001g0212 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1339-771G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921895 | ||||||
| chr6:138921976
|
A | AGT | 9 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG00673.hp2 HG00733.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1339-854_1339-853d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGT | 14 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(11): Show | 15 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1339-856_1339-853d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGT | 3 | a0001c0001t0001g0137a0001c0001t0001g0188a0001c0001t0009g0161 | 3 | HG02109.hp1 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1339-858_1339-853d others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGTG others(3): Show |
3 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018 | 3 | HG02258.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1339-862_1339-853d others(12): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGTG others(5): Show |
1 | a0002c0003t0004g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1339-864_1339-853d others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGTG others(7): Show |
1 | a0002c0003t0004g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1339-866_1339-853d others(16): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGTG others(9): Show |
8 | a0002c0003t0004g0019a0002c0003t0004g0020a0002c0003t0004g0021others(5): Show | 8 | HG01433.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339-868_1339-853d others(18): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGTG others(11): Show |
6 | a0002c0003t0004g0025a0002c0003t0004g0032a0002c0003t0004g0033others(3): Show | 6 | HG01069.hp1 HG02486.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-870_1339-853d others(20): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGTG others(13): Show |
4 | a0002c0003t0004g0022a0002c0003t0004g0027a0002c0003t0004g0030others(1): Show | 4 | HG01192.hp1 HG02056.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-872_1339-853d others(22): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGTG others(15): Show |
4 | a0002c0003t0004g0028a0002c0003t0004g0029a0002c0003t0004g0035others(1): Show | 4 | HG02015.hp2 NA18956.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-874_1339-853d others(24): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
A | AGTGTGTG others(17): Show |
1 | a0002c0003t0004g0026 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1339-876_1339-853d others(26): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
AGT | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0129a0001c0001t0001g0159others(78): Show | 82 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1339-854_1339-853d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138921976
|
AGTGTGTG others(1): Show |
A | 85 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(82): Show | 86 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.1339-860_1339-853d others(10): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138921976 | ||||||
| chr6:138922004
|
T | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1339-880A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922004 | ||||||
| chr6:138922073
|
T | C | 1 | a0001c0007t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1339-949A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922073 | ||||||
| chr6:138922137
|
T | A | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.1339-1013A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922137 | ||||||
| chr6:138922162
|
T | C | 1 | a0002c0003t0004g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1339-1038A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922162 | ||||||
| chr6:138922268
|
G | A | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-1144C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922268 | ||||||
| chr6:138922569
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1339-1445T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922569 | ||||||
| chr6:138922647
|
G | A | 1 | a0002c0003t0004g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1339-1523C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922647 | ||||||
| chr6:138922727
|
C | T | 1 | a0001c0002t0003g0328 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1339-1603G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922727 | ||||||
| chr6:138922903
|
T | C | 3 | a0003c0004t0003g0315a0003c0004t0003g0316a0003c0004t0003g0317 | 3 | HG00738.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1339-1779A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922903 | ||||||
| chr6:138922986
|
A | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(80): Show | 84 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1339-1862T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138922986 | ||||||
| chr6:138923203
|
T | C | 1 | a0001c0002t0003g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1339-2079A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138923203 | ||||||
| chr6:138923419
|
C | T | 1 | a0001c0001t0007g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1339-2295G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138923419 | ||||||
| chr6:138923430
|
T | C | 3 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018 | 3 | HG02258.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1339-2306A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138923430 | ||||||
| chr6:138923549
|
C | T | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1339-2425G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138923549 | ||||||
| chr6:138923637
|
C | T | 73 | a0001c0001t0001g0110a0001c0001t0002g0042a0001c0001t0002g0043others(70): Show | 73 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1339-2513G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138923637 | ||||||
| chr6:138923844
|
T | G | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1338+2557A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138923844 | ||||||
| chr6:138923928
|
C | CT | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1338+2472_1338+247 others(5): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138923928 | ||||||
| chr6:138924034
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+2367A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924034 | ||||||
| chr6:138924216
|
A | C | 1 | a0002c0003t0004g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1338+2185T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924216 | ||||||
| chr6:138924303
|
T | C | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1338+2098A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924303 | ||||||
| chr6:138924444
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1338+1957T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924444 | ||||||
| chr6:138924547
|
CTATGAGT others(4): Show |
C | 66 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1338+1843_1338+185 others(15): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924547 | ||||||
| chr6:138924560
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1338+1841A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924560 | ||||||
| chr6:138924617
|
C | A | 1 | a0001c0002t0003g0371 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1338+1784G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924617 | ||||||
| chr6:138924757
|
C | T | 1 | a0004c0006t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1338+1644G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924757 | ||||||
| chr6:138924904
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1338+1497C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924904 | ||||||
| chr6:138924977
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02735.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338+1424T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138924977 | ||||||
| chr6:138925060
|
A | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1338+1341T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925060 | ||||||
| chr6:138925161
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1338+1240G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925161 | ||||||
| chr6:138925175
|
G | A | 4 | a0001c0002t0003g0325a0001c0002t0003g0352a0001c0002t0003g0353others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+1226C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925175 | ||||||
| chr6:138925177
|
C | G | 66 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1338+1224G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925177 | ||||||
| chr6:138925190
|
T | TAC | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0129others(181): Show | 186 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.1338+1209_1338+121 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925190 | ||||||
| chr6:138925190
|
T | TACAC | 10 | a0001c0001t0001g0214a0001c0001t0001g0220a0001c0002t0003g0336others(7): Show | 10 | HG01346.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1338+1207_1338+121 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925190 | ||||||
| chr6:138925190
|
T | TACACAC | 19 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(16): Show | 20 | HG00738.hp2 HG02027.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.1338+1205_1338+121 others(10): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925190 | ||||||
| chr6:138925190
|
TAC | T | 69 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(66): Show | 69 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1338+1209_1338+121 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925190 | ||||||
| chr6:138925206
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1338+1195G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925206 | ||||||
| chr6:138925222
|
C | T | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1338+1179G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925222 | ||||||
| chr6:138925236
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1338+1165C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925236 | ||||||
| chr6:138925318
|
G | C | 1 | a0001c0001t0002g0051 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1338+1083C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925318 | ||||||
| chr6:138925401
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG01168.hp1 HG01169.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1338+1000C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925401 | ||||||
| chr6:138925583
|
G | A | 1 | a0001c0002t0003g0359 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1338+818C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925583 | ||||||
| chr6:138925659
|
TA | T | 80 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0170others(77): Show | 80 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1338+741delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925659 | ||||||
| chr6:138925885
|
T | C | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1338+516A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925885 | ||||||
| chr6:138925895
|
G | A | 1 | a0001c0002t0002g0120 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1338+506C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925895 | ||||||
| chr6:138925939
|
T | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(81): Show | 85 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1338+462A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138925939 | ||||||
| chr6:138926027
|
T | C | 1 | a0001c0007t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1338+374A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138926027 | ||||||
| chr6:138926067
|
TAAAG | T | 3 | a0001c0001t0001g0280a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG02040.hp1 NA19010.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1338+330_1338+333d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 10/19 | chr6 | 138926067 | ||||||
| chr6:138926654
|
A | AT | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.1258-174_1258-173i others(3): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138926654 | ||||||
| chr6:138927119
|
C | T | 7 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0058others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1258-638G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927119 | ||||||
| chr6:138927164
|
TC | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1258-684delG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927164 | ||||||
| chr6:138927243
|
A | G | 1 | a0001c0002t0002g0122 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1258-762T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927243 | ||||||
| chr6:138927335
|
T | A | 27 | a0002c0003t0004g0016a0002c0003t0004g0018a0002c0003t0004g0019others(24): Show | 27 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1258-854A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927335 | ||||||
| chr6:138927502
|
G | A | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1258-1021C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927502 | ||||||
| chr6:138927585
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0045 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1258-1104A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927585 | ||||||
| chr6:138927642
|
C | T | 3 | a0001c0001t0007g0053a0001c0001t0007g0062a0001c0001t0007g0085 | 3 | HG00280.hp1 HG00323.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1258-1161G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927642 | ||||||
| chr6:138927723
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0168 | 3 | HG00558.hp2 HG00597.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1258-1242A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927723 | ||||||
| chr6:138927763
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1258-1282T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138927763 | ||||||
| chr6:138928011
|
A | G | 16 | a0001c0001t0001g0194a0002c0003t0004g0026a0002c0003t0004g0027others(13): Show | 16 | HG01069.hp1 HG01192.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1258-1530T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928011 | ||||||
| chr6:138928054
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1258-1573A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928054 | ||||||
| chr6:138928236
|
G | A | 1 | a0001c0001t0023g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1257+1741C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928236 | ||||||
| chr6:138928359
|
T | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1257+1618A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928359 | ||||||
| chr6:138928396
|
A | T | 1 | a0001c0002t0003g0373 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1257+1581T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928396 | ||||||
| chr6:138928492
|
T | C | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1257+1485A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928492 | ||||||
| chr6:138928494
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1257+1483A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928494 | ||||||
| chr6:138928496
|
GA | G | 18 | a0001c0002t0003g0338a0001c0002t0003g0378a0001c0002t0003g0379others(15): Show | 18 | HG01069.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1257+1480delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928496 | ||||||
| chr6:138928537
|
A | G | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.1257+1440T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928537 | ||||||
| chr6:138928538
|
T | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(82): Show | 86 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1257+1439A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928538 | ||||||
| chr6:138928688
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1257+1289A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928688 | ||||||
| chr6:138928796
|
T | TCAA | 87 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(84): Show | 88 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.1257+1178_1257+118 others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928796 | ||||||
| chr6:138928906
|
G | T | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1257+1071C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928906 | ||||||
| chr6:138928945
|
T | C | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1257+1032A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928945 | ||||||
| chr6:138928960
|
T | C | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1257+1017A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928960 | ||||||
| chr6:138928988
|
C | G | 65 | a0001c0002t0003g0318a0001c0002t0003g0319a0001c0002t0003g0320others(62): Show | 65 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1257+989G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138928988 | ||||||
| chr6:138929307
|
C | A | 1 | a0001c0001t0001g0232 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1257+670G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138929307 | ||||||
| chr6:138929316
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1257+661A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138929316 | ||||||
| chr6:138929322
|
T | A | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1257+655A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138929322 | ||||||
| chr6:138929382
|
G | T | 193 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0159others(190): Show | 194 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.1257+595C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138929382 | ||||||
| chr6:138929409
|
T | C | 1 | a0001c0002t0003g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1257+568A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138929409 | ||||||
| chr6:138929621
|
T | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257+356A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138929621 | ||||||
| chr6:138929642
|
T | C | 1 | a0001c0002t0005g0312 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1257+335A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138929642 | ||||||
| chr6:138929735
|
G | A | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257+242C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 9/19 | chr6 | 138929735 | ||||||
| chr6:138930180
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1136-82G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930180 | ||||||
| chr6:138930517
|
G | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0268 | 3 | HG02698.hp1 HG04199.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1136-419C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930517 | ||||||
| chr6:138930526
|
T | C | 1 | a0001c0002t0005g0311 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1136-428A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930526 | ||||||
| chr6:138930580
|
C | T | 1 | a0001c0002t0017g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1136-482G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930580 | ||||||
| chr6:138930615
|
A | C | 6 | a0001c0002t0003g0334a0001c0002t0003g0338a0001c0002t0003g0340others(3): Show | 6 | NA18946.hp1 NA18980.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1136-517T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930615 | ||||||
| chr6:138930697
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(5): Show | 9 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1136-599T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930697 | ||||||
| chr6:138930730
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1136-632G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930730 | ||||||
| chr6:138930753
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1136-655T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930753 | ||||||
| chr6:138930936
|
T | C | 3 | a0003c0004t0003g0315a0003c0004t0003g0316a0003c0004t0003g0317 | 3 | HG00738.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1136-838A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138930936 | ||||||
| chr6:138931083
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1136-985A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138931083 | ||||||
| chr6:138931101
|
A | G | 1 | a0001c0002t0003g0332 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1136-1003T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138931101 | ||||||
| chr6:138931121
|
T | C | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1136-1023A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138931121 | ||||||
| chr6:138931387
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(81): Show | 85 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1136-1289G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138931387 | ||||||
| chr6:138931453
|
T | C | 66 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1136-1355A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138931453 | ||||||
| chr6:138931768
|
G | GA | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1136-1671dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138931768 | ||||||
| chr6:138931917
|
G | A | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-1819C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138931917 | ||||||
| chr6:138932018
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1136-1920T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932018 | ||||||
| chr6:138932097
|
C | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136-1999G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932097 | ||||||
| chr6:138932212
|
T | A | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1136-2114A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932212 | ||||||
| chr6:138932306
|
C | CCTTT | 187 | a0001c0001t0001g0110a0001c0001t0001g0194a0001c0001t0002g0042others(184): Show | 188 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.1136-2209_1136-220 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932306 | ||||||
| chr6:138932459
|
A | AC | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 101 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.1136-2362dupG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932459 | ||||||
| chr6:138932459
|
AC | A | 86 | a0001c0001t0001g0245a0001c0001t0002g0054a0001c0001t0003g0324others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.1136-2362delG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932459 | ||||||
| chr6:138932480
|
C | T | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-2382G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932480 | ||||||
| chr6:138932570
|
A | G | 29 | a0001c0001t0001g0194a0002c0003t0004g0016a0002c0003t0004g0017others(26): Show | 29 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.1136-2472T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932570 | ||||||
| chr6:138932766
|
C | T | 1 | a0002c0003t0004g0033 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1136-2668G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932766 | ||||||
| chr6:138932769
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1136-2671C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932769 | ||||||
| chr6:138932803
|
T | C | 2 | a0001c0001t0001g0139a0009c0008t0001g0138 | 2 | HG00639.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1136-2705A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932803 | ||||||
| chr6:138932873
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1136-2775T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138932873 | ||||||
| chr6:138933016
|
C | G | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.1136-2918G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933016 | ||||||
| chr6:138933120
|
C | A | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1136-3022G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933120 | ||||||
| chr6:138933180
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1136-3082C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933180 | ||||||
| chr6:138933326
|
T | C | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-3228A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933326 | ||||||
| chr6:138933540
|
G | GCTTA | 77 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(74): Show | 78 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1136-3446_1136-344 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933540 | ||||||
| chr6:138933563
|
T | C | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1136-3465A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933563 | ||||||
| chr6:138933648
|
G | T | 4 | a0001c0002t0003g0347a0001c0002t0003g0348a0001c0002t0003g0349others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-3550C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933648 | ||||||
| chr6:138933900
|
TAA | T | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136-3804_1136-380 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933900 | ||||||
| chr6:138933928
|
G | A | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.1136-3830C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138933928 | ||||||
| chr6:138934378
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1136-4280C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934378 | ||||||
| chr6:138934387
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1136-4289G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934387 | ||||||
| chr6:138934455
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1136-4357G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934455 | ||||||
| chr6:138934456
|
G | A | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1136-4358C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934456 | ||||||
| chr6:138934467
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1136-4369G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934467 | ||||||
| chr6:138934648
|
T | G | 2 | a0002c0003t0004g0022a0002c0003t0004g0023 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1136-4550A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934648 | ||||||
| chr6:138934677
|
G | C | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1136-4579C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934677 | ||||||
| chr6:138934707
|
C | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1136-4609G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934707 | ||||||
| chr6:138934798
|
T | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1136-4700A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934798 | ||||||
| chr6:138934817
|
CATT | C | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1136-4722_1136-472 others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934817 | ||||||
| chr6:138934852
|
C | T | 191 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(188): Show | 192 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.1136-4754G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138934852 | ||||||
| chr6:138935355
|
G | T | 1 | a0001c0001t0001g0289 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1136-5257C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935355 | ||||||
| chr6:138935429
|
A | G | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1136-5331T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935429 | ||||||
| chr6:138935470
|
T | C | 33 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(30): Show | 33 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.1136-5372A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935470 | ||||||
| chr6:138935620
|
C | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1136-5522G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935620 | ||||||
| chr6:138935621
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1136-5523G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935621 | ||||||
| chr6:138935627
|
A | G | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 312 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(309): Show |
intron_variant | MODIFIER | c.1136-5529T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935627 | ||||||
| chr6:138935637
|
C | A | 1 | a0001c0001t0001g0242 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1136-5539G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935637 | ||||||
| chr6:138935643
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1136-5545G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935643 | ||||||
| chr6:138935782
|
A | G | 1 | a0001c0002t0003g0378 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1135+5553T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935782 | ||||||
| chr6:138935783
|
G | T | 3 | a0001c0001t0001g0264a0001c0001t0001g0274a0001c0001t0001g0286 | 3 | NA18981.hp1 NA19009.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1135+5552C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935783 | ||||||
| chr6:138935818
|
C | T | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1135+5517G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935818 | ||||||
| chr6:138935853
|
T | TGGCGGGG | 3 | a0001c0002t0003g0337a0001c0002t0003g0364a0001c0002t0003g0365 | 3 | NA18979.hp1 NA18981.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1135+5475_1135+548 others(11): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935853 | ||||||
| chr6:138935853
|
T | TGGTGGGG others(4): Show |
1 | a0001c0002t0003g0331 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1135+5481_1135+548 others(15): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935853 | ||||||
| chr6:138935856
|
C | CG | 76 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(73): Show | 76 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1135+5478dupC | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935856
|
C | CGG | 24 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0229others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1135+5477_1135+547 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935856
|
C | CGGGGGGG others(3): Show |
10 | a0001c0002t0002g0123a0001c0002t0003g0328a0001c0002t0003g0330others(7): Show | 10 | HG02976.hp1 HG03225.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135+5469_1135+547 others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935856
|
C | CGGGGGGG others(4): Show |
7 | a0001c0002t0003g0332a0001c0002t0003g0334a0001c0002t0003g0338others(4): Show | 7 | HG02897.hp1 HG03927.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135+5468_1135+547 others(15): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935856
|
C | CGGGGGGG others(5): Show |
9 | a0001c0002t0003g0329a0001c0002t0003g0333a0001c0002t0003g0343others(6): Show | 9 | HG02630.hp1 HG03486.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.1135+5467_1135+547 others(16): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935856
|
C | CGGGGGGG others(6): Show |
3 | a0001c0002t0003g0318a0001c0002t0003g0369a0001c0002t0003g0372 | 3 | HG02040.hp2 HG02055.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1135+5478_1135+547 others(17): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935856
|
C | CGGGGGGG others(7): Show |
3 | a0001c0002t0003g0340a0001c0002t0003g0366a0001c0002t0014g0386 | 3 | HG03486.hp1 NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1135+5478_1135+547 others(18): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935856
|
C | CGGGGGGG others(8): Show |
3 | a0001c0002t0003g0327a0001c0002t0003g0361a0001c0002t0003g0367 | 3 | HG02615.hp1 HG03942.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1135+5478_1135+547 others(19): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935856
|
C | G | 1 | a0001c0002t0003g0331 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1135+5479G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935856 | ||||||
| chr6:138935857
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1135+5478C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935857 | ||||||
| chr6:138935859
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0289 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1135+5476C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935859 | ||||||
| chr6:138935860
|
G | T | 1 | a0001c0013t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1135+5475C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935860 | ||||||
| chr6:138935862
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1135+5473C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935862 | ||||||
| chr6:138935866
|
GGGC | G | 23 | a0001c0013t0001g0130a0002c0003t0004g0016a0002c0003t0004g0017others(20): Show | 23 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1135+5466_1135+546 others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935866 | ||||||
| chr6:138935868
|
GC | G | 55 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0140others(52): Show | 55 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1135+5466delG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935868 | ||||||
| chr6:138935869
|
C | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(268): Show | 275 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.1135+5466G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935869 | ||||||
| chr6:138935869
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0191a0001c0001t0001g0291 | 3 | HG02622.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1135+5466G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935869 | ||||||
| chr6:138935870
|
G | GGGGGGGG others(5): Show |
1 | a0001c0002t0003g0373 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1135+5464_1135+546 others(16): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935870 | ||||||
| chr6:138935870
|
G | GGGGGGGG others(7): Show |
1 | a0001c0002t0003g0376 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1135+5464_1135+546 others(18): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935870 | ||||||
| chr6:138935870
|
G | GGGGGGGG others(8): Show |
1 | a0001c0002t0003g0368 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1135+5464_1135+546 others(19): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935870 | ||||||
| chr6:138935870
|
G | GGGGGGGG others(6): Show |
1 | a0001c0002t0003g0379 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1135+5464_1135+546 others(17): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935870 | ||||||
| chr6:138935871
|
C | G | 7 | a0001c0001t0001g0225a0001c0001t0002g0048a0001c0001t0002g0068others(4): Show | 7 | HG00423.hp2 HG01261.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1135+5464G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935871 | ||||||
| chr6:138935871
|
C | T | 3 | a0001c0002t0003g0378a0001c0002t0015g0383a0001c0002t0015g0384 | 3 | HG02451.hp2 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1135+5464G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935871 | ||||||
| chr6:138935872
|
G | A | 1 | a0004c0006t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1135+5463C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935872 | ||||||
| chr6:138935879
|
T | C | 2 | a0001c0002t0003g0321a0001c0002t0003g0374 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1135+5456A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935879 | ||||||
| chr6:138935913
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1135+5422A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138935913 | ||||||
| chr6:138936187
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+5148A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936187 | ||||||
| chr6:138936191
|
A | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG01168.hp1 HG01169.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1135+5144T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936191 | ||||||
| chr6:138936223
|
C | T | 60 | a0001c0002t0003g0318a0001c0002t0003g0319a0001c0002t0003g0320others(57): Show | 60 | HG00423.hp2 HG00438.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.1135+5112G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936223 | ||||||
| chr6:138936224
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1135+5111C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936224 | ||||||
| chr6:138936270
|
G | T | 1 | a0002c0003t0004g0037 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1135+5065C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936270 | ||||||
| chr6:138936278
|
G | A | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1135+5057C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936278 | ||||||
| chr6:138936322
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1135+5013G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936322 | ||||||
| chr6:138936464
|
A | C | 1 | a0001c0002t0017g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1135+4871T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936464 | ||||||
| chr6:138936480
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1135+4855A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936480 | ||||||
| chr6:138936581
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0186 | 2 | HG00544.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1135+4754G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936581 | ||||||
| chr6:138936590
|
G | T | 77 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(74): Show | 78 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.1135+4745C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936590 | ||||||
| chr6:138936593
|
G | C | 1 | a0001c0001t0002g0082 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1135+4742C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936593 | ||||||
| chr6:138936603
|
G | A | 67 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(64): Show | 67 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1135+4732C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936603 | ||||||
| chr6:138936622
|
T | TGG | 61 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(58): Show | 62 | HG00741.hp1 HG01891.hp1 HG02027.hp1 others(59): Show |
intron_variant | MODIFIER | c.1135+4711_1135+471 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936622 | ||||||
| chr6:138936625
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135+4710C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936625 | ||||||
| chr6:138936628
|
G | GGA | 33 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(30): Show | 33 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.1135+4706_1135+470 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936628 | ||||||
| chr6:138936643
|
G | A | 1 | a0001c0002t0003g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1135+4692C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936643 | ||||||
| chr6:138936695
|
A | AT | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+4639dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936695 | ||||||
| chr6:138936729
|
C | T | 191 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(188): Show | 192 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.1135+4606G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936729 | ||||||
| chr6:138936877
|
T | C | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1135+4458A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936877 | ||||||
| chr6:138936902
|
A | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0069 | 2 | NA18943.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1135+4433T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138936902 | ||||||
| chr6:138937056
|
A | G | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1135+4279T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937056 | ||||||
| chr6:138937107
|
G | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+4228C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937107 | ||||||
| chr6:138937108
|
G | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+4227C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937108 | ||||||
| chr6:138937109
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+4226C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937109 | ||||||
| chr6:138937110
|
AAACT | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+4221_1135+422 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937110 | ||||||
| chr6:138937115
|
C | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+4220G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937115 | ||||||
| chr6:138937121
|
A | G | 2 | a0002c0003t0012g0307a0002c0003t0012g0308 | 2 | HG01069.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1135+4214T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937121 | ||||||
| chr6:138937248
|
G | C | 5 | a0002c0003t0004g0019a0002c0003t0004g0020a0002c0003t0004g0021others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+4087C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937248 | ||||||
| chr6:138937445
|
A | G | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.1135+3890T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937445 | ||||||
| chr6:138937463
|
T | C | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1135+3872A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937463 | ||||||
| chr6:138937521
|
T | TA | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+3813dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937521 | ||||||
| chr6:138937602
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0045 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1135+3733A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937602 | ||||||
| chr6:138937649
|
A | G | 1 | a0001c0001t0018g0012 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1135+3686T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937649 | ||||||
| chr6:138937724
|
A | T | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1135+3611T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937724 | ||||||
| chr6:138937744
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1135+3591A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937744 | ||||||
| chr6:138937784
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1135+3551A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937784 | ||||||
| chr6:138937912
|
A | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+3423T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937912 | ||||||
| chr6:138937930
|
G | C | 1 | a0001c0001t0001g0196 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1135+3405C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937930 | ||||||
| chr6:138937972
|
T | C | 1 | a0002c0003t0004g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1135+3363A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937972 | ||||||
| chr6:138937980
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1135+3355G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937980 | ||||||
| chr6:138937981
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+3354C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138937981 | ||||||
| chr6:138938005
|
C | CT | 194 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0129others(191): Show | 196 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.1135+3329dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938005 | ||||||
| chr6:138938018
|
A | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+3317T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938018 | ||||||
| chr6:138938066
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1135+3269G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938066 | ||||||
| chr6:138938179
|
T | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(82): Show | 86 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1135+3156A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938179 | ||||||
| chr6:138938224
|
G | A | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1135+3111C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938224 | ||||||
| chr6:138938357
|
C | T | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1135+2978G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938357 | ||||||
| chr6:138938502
|
T | C | 2 | a0001c0002t0003g0340a0001c0002t0003g0358 | 2 | NA18946.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1135+2833A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938502 | ||||||
| chr6:138938627
|
G | A | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG00733.hp1 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135+2708C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938627 | ||||||
| chr6:138938703
|
G | T | 2 | a0001c0002t0003g0321a0001c0002t0003g0374 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1135+2632C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938703 | ||||||
| chr6:138938839
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0185 | 2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1135+2496G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938839 | ||||||
| chr6:138938850
|
AT | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(160): Show | 165 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1135+2484delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938850 | ||||||
| chr6:138938933
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+2402G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938933 | ||||||
| chr6:138938952
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+2383T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938952 | ||||||
| chr6:138938985
|
C | A | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1135+2350G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138938985 | ||||||
| chr6:138939033
|
T | G | 1 | a0001c0001t0006g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1135+2302A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939033 | ||||||
| chr6:138939047
|
G | A | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1135+2288C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939047 | ||||||
| chr6:138939281
|
GA | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1135+2053delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939281 | ||||||
| chr6:138939282
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1135+2053T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939282 | ||||||
| chr6:138939530
|
G | A | 1 | a0001c0013t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1135+1805C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939530 | ||||||
| chr6:138939546
|
G | A | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135+1789C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939546 | ||||||
| chr6:138939554
|
C | T | 67 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(64): Show | 67 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1135+1781G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939554 | ||||||
| chr6:138939650
|
A | G | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1135+1685T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939650 | ||||||
| chr6:138939859
|
C | CAACT | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+1472_1135+147 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939859 | ||||||
| chr6:138939950
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1135+1385G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138939950 | ||||||
| chr6:138940156
|
T | C | 11 | a0001c0001t0002g0049a0001c0001t0002g0063a0001c0001t0002g0067others(8): Show | 11 | HG00639.hp1 HG01496.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135+1179A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940156 | ||||||
| chr6:138940165
|
C | T | 4 | a0002c0003t0004g0032a0002c0003t0004g0033a0002c0003t0004g0034others(1): Show | 4 | NA18966.hp1 NA18968.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135+1170G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940165 | ||||||
| chr6:138940228
|
T | C | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135+1107A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940228 | ||||||
| chr6:138940242
|
T | C | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1135+1093A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940242 | ||||||
| chr6:138940250
|
C | T | 1 | a0001c0002t0003g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1135+1085G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940250 | ||||||
| chr6:138940277
|
A | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+1058T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940277 | ||||||
| chr6:138940340
|
G | A | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(290): Show | 297 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(294): Show |
intron_variant | MODIFIER | c.1135+995C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940340 | ||||||
| chr6:138940349
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1135+986A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940349 | ||||||
| chr6:138940489
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1135+846C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940489 | ||||||
| chr6:138940574
|
A | G | 7 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0058others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135+761T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940574 | ||||||
| chr6:138940615
|
C | T | 29 | a0001c0001t0001g0194a0002c0003t0004g0016a0002c0003t0004g0017others(26): Show | 29 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.1135+720G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940615 | ||||||
| chr6:138940670
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+665G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940670 | ||||||
| chr6:138940694
|
C | T | 1 | a0001c0001t0003g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1135+641G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940694 | ||||||
| chr6:138940772
|
G | C | 1 | a0001c0001t0003g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1135+563C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940772 | ||||||
| chr6:138940778
|
GAAGA | G | 3 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018 | 3 | HG02258.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1135+553_1135+556d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940778 | ||||||
| chr6:138940896
|
G | T | 377 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(374): Show | 381 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(378): Show |
intron_variant | MODIFIER | c.1135+439C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940896 | ||||||
| chr6:138940926
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1135+409T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138940926 | ||||||
| chr6:138941018
|
T | C | 187 | a0001c0001t0001g0194a0001c0001t0002g0042a0001c0001t0002g0043others(184): Show | 188 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.1135+317A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138941018 | ||||||
| chr6:138941249
|
T | C | 1 | a0001c0001t0001g0242 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1135+86A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 8/19 | chr6 | 138941249 | ||||||
| chr6:138941513
|
T | C | 1 | a0004c0006t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.981-24A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138941513 | ||||||
| chr6:138941661
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.981-172G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138941661 | ||||||
| chr6:138941679
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.981-190T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138941679 | ||||||
| chr6:138941807
|
G | A | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG00733.hp1 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.981-318C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138941807 | ||||||
| chr6:138941810
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0255 | 2 | HG00438.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.981-321T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138941810 | ||||||
| chr6:138941953
|
A | C | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.981-464T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138941953 | ||||||
| chr6:138941981
|
T | C | 115 | a0001c0001t0001g0194a0001c0001t0003g0324a0001c0002t0002g0001others(112): Show | 116 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(113): Show |
intron_variant | MODIFIER | c.981-492A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138941981 | ||||||
| chr6:138942029
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.981-540A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942029 | ||||||
| chr6:138942035
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01109.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.981-546A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942035 | ||||||
| chr6:138942064
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.981-575G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942064 | ||||||
| chr6:138942120
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.981-631G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942120 | ||||||
| chr6:138942135
|
G | A | 3 | a0001c0001t0001g0221a0001c0002t0003g0378a0001c0002t0003g0379 | 3 | HG02145.hp1 HG02451.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.981-646C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942135 | ||||||
| chr6:138942230
|
T | C | 1 | a0001c0013t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.981-741A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942230 | ||||||
| chr6:138942426
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.981-937T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942426 | ||||||
| chr6:138942428
|
G | C | 1 | a0001c0013t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.981-939C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942428 | ||||||
| chr6:138942908
|
C | A | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG00733.hp1 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.980+605G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942908 | ||||||
| chr6:138942945
|
A | C | 85 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(82): Show | 86 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.980+568T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138942945 | ||||||
| chr6:138943046
|
C | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.980+467G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138943046 | ||||||
| chr6:138943140
|
G | A | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.980+373C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138943140 | ||||||
| chr6:138943167
|
A | G | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.980+346T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138943167 | ||||||
| chr6:138943184
|
T | C | 1 | a0001c0002t0003g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.980+329A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138943184 | ||||||
| chr6:138943204
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.980+309T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138943204 | ||||||
| chr6:138943272
|
A | G | 2 | a0001c0002t0003g0318a0001c0002t0003g0327 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.980+241T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138943272 | ||||||
| chr6:138943295
|
T | C | 1 | a0001c0001t0002g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.980+218A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 7/19 | chr6 | 138943295 | ||||||
| chr6:138943696
|
T | C | 1 | a0001c0002t0003g0355 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.917-120A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 6/19 | chr6 | 138943696 | ||||||
| chr6:138943793
|
T | G | 112 | a0001c0001t0001g0194a0001c0002t0002g0001a0001c0002t0002g0116others(109): Show | 113 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(110): Show |
intron_variant | MODIFIER | c.916+60A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 6/19 | chr6 | 138943793 | ||||||
| chr6:138944050
|
T | A | 1 | a0001c0001t0001g0304 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.754-35A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 5/19 | chr6 | 138944050 | ||||||
| chr6:138944142
|
C | T | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(301): Show | 308 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(305): Show |
intron_variant | MODIFIER | c.754-127G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 5/19 | chr6 | 138944142 | ||||||
| chr6:138944195
|
G | A | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.754-180C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 5/19 | chr6 | 138944195 | ||||||
| chr6:138944255
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-240T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 5/19 | chr6 | 138944255 | ||||||
| chr6:138944361
|
A | G | 84 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(81): Show | 85 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.753+137T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 5/19 | chr6 | 138944361 | ||||||
| chr6:138944439
|
G | A | 1 | a0001c0001t0022g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.753+59C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 5/19 | chr6 | 138944439 | ||||||
| chr6:138944745
|
T | A | 186 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(183): Show | 187 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.629-123A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 4/19 | chr6 | 138944745 | ||||||
| chr6:138944997
|
A | C | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.628+222T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 4/19 | chr6 | 138944997 | ||||||
| chr6:138945157
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0101 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.628+62G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 4/19 | chr6 | 138945157 | ||||||
| chr6:138945952
|
G | A | 1 | a0001c0002t0003g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278-255C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138945952 | ||||||
| chr6:138945996
|
G | C | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.278-299C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138945996 | ||||||
| chr6:138946030
|
A | T | 81 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(78): Show | 82 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.278-333T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946030 | ||||||
| chr6:138946082
|
C | G | 1 | a0001c0002t0003g0345 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.278-385G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946082 | ||||||
| chr6:138946252
|
T | A | 1 | a0001c0001t0001g0181 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.278-555A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946252 | ||||||
| chr6:138946264
|
A | C | 1 | a0001c0001t0001g0181 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.278-567T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946264 | ||||||
| chr6:138946274
|
T | TAC | 188 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(185): Show | 189 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.278-578_278-577ins others(2): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946274 | ||||||
| chr6:138946333
|
T | C | 1 | a0001c0002t0008g0119 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.278-636A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946333 | ||||||
| chr6:138946395
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-698C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946395 | ||||||
| chr6:138946423
|
G | A | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.278-726C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946423 | ||||||
| chr6:138946449
|
G | A | 15 | a0002c0003t0004g0026a0002c0003t0004g0027a0002c0003t0004g0028others(12): Show | 15 | HG01069.hp1 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.278-752C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946449 | ||||||
| chr6:138946484
|
G | C | 83 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(80): Show | 84 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.278-787C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946484 | ||||||
| chr6:138946632
|
C | T | 111 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(108): Show | 112 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(109): Show |
intron_variant | MODIFIER | c.278-935G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946632 | ||||||
| chr6:138946714
|
G | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0275 | 2 | HG00673.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.278-1017C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946714 | ||||||
| chr6:138946739
|
C | A | 1 | a0001c0002t0003g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.278-1042G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946739 | ||||||
| chr6:138946739
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.278-1042G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946739 | ||||||
| chr6:138946871
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 250 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(247): Show |
intron_variant | MODIFIER | c.277+919G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138946871 | ||||||
| chr6:138947035
|
G | GCT | 73 | a0001c0001t0001g0003a0001c0001t0001g0110a0001c0001t0001g0126others(70): Show | 74 | HG00544.hp2 HG00609.hp1 HG01074.hp2 others(71): Show |
intron_variant | MODIFIER | c.277+753_277+754dup others(2): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
G | GCTCT | 18 | a0001c0001t0001g0128a0001c0001t0001g0136a0001c0001t0001g0139others(15): Show | 18 | HG00639.hp2 HG00733.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.277+751_277+754dup others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
G | GCTCTCT | 7 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG00544.hp1 HG02056.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+749_277+754dup others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
G | GCTCTCTC others(1): Show |
3 | a0001c0001t0001g0142a0001c0001t0001g0229a0001c0001t0001g0235 | 3 | HG02698.hp1 HG02976.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.277+747_277+754dup others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
G | GCTCTCTC others(3): Show |
1 | a0001c0001t0001g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.277+745_277+754dup others(10): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
G | GCTCTCTC others(25): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0301 | 3 | HG01884.hp2 HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.277+723_277+754dup others(32): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
G | GCTCTCTC others(27): Show |
1 | a0001c0001t0001g0302 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277+721_277+754dup others(34): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
G | GCTCTCTC others(31): Show |
1 | a0001c0001t0001g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.277+717_277+754dup others(38): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
G | GCTCTCTC others(11): Show |
3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.277+754_277+755ins others(18): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
GCT | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0207a0001c0001t0001g0211others(1): Show | 4 | HG01934.hp2 HG03710.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+753_277+754del others(2): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
GCTCT | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0135a0001c0001t0001g0145others(4): Show | 8 | HG01106.hp2 HG01261.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+751_277+754del others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
GCTCTCT | G | 35 | a0001c0001t0001g0131a0001c0001t0002g0046a0001c0001t0002g0047others(32): Show | 35 | HG01069.hp1 HG01192.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.277+749_277+754del others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
GCTCTCTC others(1): Show |
G | 67 | a0001c0001t0001g0129a0001c0001t0001g0210a0001c0001t0002g0042others(64): Show | 67 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.277+747_277+754del others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
GCTCTCTC others(3): Show |
G | 86 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0168others(83): Show | 87 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.277+745_277+754del others(10): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
GCTCTCTC others(5): Show |
G | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0002t0014g0385others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+743_277+754del others(12): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947035
|
GCTCTCTC others(7): Show |
G | 1 | a0001c0002t0003g0349 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.277+741_277+754del others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947035 | ||||||
| chr6:138947041
|
T | TCTCTCTC others(3): Show |
1 | a0001c0007t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.277+748_277+749ins others(10): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947041 | ||||||
| chr6:138947236
|
C | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 7 | HG01106.hp2 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+554G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947236 | ||||||
| chr6:138947357
|
A | G | 1 | a0004c0006t0001g0290 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.277+433T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947357 | ||||||
| chr6:138947377
|
AC | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.277+412delG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 2/19 | chr6 | 138947377 | ||||||
| chr6:138948281
|
C | T | 2 | a0001c0001t0022g0099a0001c0001t0023g0098 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.154-368G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948281 | ||||||
| chr6:138948349
|
T | C | 72 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.154-436A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948349 | ||||||
| chr6:138948393
|
T | A | 185 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(182): Show | 186 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.154-480A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948393 | ||||||
| chr6:138948443
|
T | C | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.154-530A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948443 | ||||||
| chr6:138948621
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154-708A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948621 | ||||||
| chr6:138948732
|
T | G | 77 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(74): Show | 78 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.154-819A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948732 | ||||||
| chr6:138948733
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-820A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948733 | ||||||
| chr6:138948858
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-945A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948858 | ||||||
| chr6:138948990
|
T | C | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.154-1077A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138948990 | ||||||
| chr6:138949077
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.154-1164G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138949077 | ||||||
| chr6:138949110
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0235 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.154-1197G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138949110 | ||||||
| chr6:138949675
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0305 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.154-1762C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138949675 | ||||||
| chr6:138949727
|
TA | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 185 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.154-1815delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138949727 | ||||||
| chr6:138949727
|
TAA | T | 113 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(110): Show | 114 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(111): Show |
intron_variant | MODIFIER | c.154-1816_154-1815d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138949727 | ||||||
| chr6:138949739
|
A | G | 1 | a0001c0002t0005g0312 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.154-1826T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138949739 | ||||||
| chr6:138949741
|
G | T | 1 | a0001c0002t0005g0312 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.154-1828C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138949741 | ||||||
| chr6:138950013
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154-2100T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950013 | ||||||
| chr6:138950178
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 112 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.154-2265A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950178 | ||||||
| chr6:138950467
|
C | G | 1 | a0001c0002t0003g0359 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.154-2554G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950467 | ||||||
| chr6:138950513
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.154-2600A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950513 | ||||||
| chr6:138950597
|
C | A | 84 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(81): Show | 85 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.154-2684G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950597 | ||||||
| chr6:138950687
|
C | T | 15 | a0002c0003t0004g0026a0002c0003t0004g0027a0002c0003t0004g0028others(12): Show | 15 | HG01069.hp1 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.154-2774G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950687 | ||||||
| chr6:138950730
|
T | C | 77 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(74): Show | 78 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.154-2817A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950730 | ||||||
| chr6:138950910
|
G | A | 2 | a0001c0001t0022g0099a0001c0001t0023g0098 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.154-2997C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950910 | ||||||
| chr6:138950911
|
C | A | 2 | a0001c0001t0022g0099a0001c0001t0023g0098 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.154-2998G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950911 | ||||||
| chr6:138950911
|
C | T | 67 | a0001c0001t0001g0241a0001c0001t0001g0273a0001c0001t0003g0324others(64): Show | 68 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.154-2998G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950911 | ||||||
| chr6:138950924
|
C | T | 1 | a0004c0006t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.154-3011G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950924 | ||||||
| chr6:138950938
|
C | T | 79 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(76): Show | 79 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.154-3025G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950938 | ||||||
| chr6:138950965
|
G | A | 21 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(18): Show | 21 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.154-3052C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950965 | ||||||
| chr6:138950990
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.154-3077G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950990 | ||||||
| chr6:138950991
|
C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(53): Show | 57 | HG00423.hp2 HG00741.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.154-3078G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950991 | ||||||
| chr6:138950992
|
G | A | 23 | a0001c0001t0001g0172a0001c0001t0003g0324a0001c0001t0019g0013others(20): Show | 24 | HG00738.hp2 HG02027.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.154-3079C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138950992 | ||||||
| chr6:138951044
|
G | A | 1 | a0002c0003t0004g0017 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.154-3131C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951044 | ||||||
| chr6:138951111
|
C | CG | 76 | a0001c0001t0001g0145a0001c0002t0002g0001a0001c0002t0002g0116others(73): Show | 77 | HG00423.hp2 HG00438.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.154-3199dupC | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951111 | ||||||
| chr6:138951137
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.154-3224C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951137 | ||||||
| chr6:138951164
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01109.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.154-3251C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951164 | ||||||
| chr6:138951466
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-3553A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951466 | ||||||
| chr6:138951476
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.154-3563C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951476 | ||||||
| chr6:138951512
|
A | C | 1 | a0001c0001t0002g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.154-3599T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951512 | ||||||
| chr6:138951586
|
T | C | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-3673A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951586 | ||||||
| chr6:138951610
|
C | A | 1 | a0001c0002t0003g0318 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154-3697G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951610 | ||||||
| chr6:138951903
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-3990C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951903 | ||||||
| chr6:138951953
|
T | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0186others(1): Show | 4 | HG00544.hp1 NA18939.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-4040A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951953 | ||||||
| chr6:138951992
|
G | A | 29 | a0001c0001t0001g0157a0002c0003t0004g0016a0002c0003t0004g0017others(26): Show | 29 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-4079C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138951992 | ||||||
| chr6:138952047
|
A | C | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.154-4134T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952047 | ||||||
| chr6:138952145
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.154-4232C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952145 | ||||||
| chr6:138952311
|
A | C | 90 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(87): Show | 90 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.154-4398T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952311 | ||||||
| chr6:138952422
|
A | G | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 322 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(319): Show |
intron_variant | MODIFIER | c.154-4509T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952422 | ||||||
| chr6:138952457
|
T | C | 1 | a0001c0001t0003g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.154-4544A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952457 | ||||||
| chr6:138952642
|
C | A | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 201 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.154-4729G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952642 | ||||||
| chr6:138952741
|
T | C | 1 | a0001c0001t0011g0259 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.154-4828A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952741 | ||||||
| chr6:138952792
|
C | T | 31 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0199others(28): Show | 31 | HG00639.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.154-4879G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952792 | ||||||
| chr6:138952803
|
T | C | 353 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(350): Show | 357 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(354): Show |
intron_variant | MODIFIER | c.154-4890A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952803 | ||||||
| chr6:138952834
|
G | GT | 16 | a0001c0001t0001g0128a0001c0001t0001g0163a0001c0001t0001g0176others(13): Show | 16 | HG01891.hp1 HG02027.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-4922dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952834 | ||||||
| chr6:138952834
|
G | T | 2 | a0001c0001t0001g0110a0001c0007t0001g0158 | 2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.154-4921C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952834 | ||||||
| chr6:138952834
|
GT | G | 27 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(24): Show | 27 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.154-4922delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952834 | ||||||
| chr6:138952907
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.154-4994C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138952907 | ||||||
| chr6:138953128
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.154-5215G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953128 | ||||||
| chr6:138953165
|
T | A | 1 | a0001c0002t0003g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154-5252A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953165 | ||||||
| chr6:138953207
|
T | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.154-5294A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953207 | ||||||
| chr6:138953298
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.154-5385T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953298 | ||||||
| chr6:138953322
|
C | T | 1 | a0001c0002t0003g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154-5409G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953322 | ||||||
| chr6:138953680
|
TCAA | T | 80 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(77): Show | 81 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.154-5770_154-5768d others(5): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953680 | ||||||
| chr6:138953680
|
TCAAA | T | 4 | a0001c0001t0003g0324a0001c0002t0003g0375a0005c0005t0003g0322others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-5771_154-5768d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953680 | ||||||
| chr6:138953681
|
CA | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 142 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.154-5769delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953681 | ||||||
| chr6:138953681
|
CAA | C | 85 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(82): Show | 85 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.154-5770_154-5769d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953681 | ||||||
| chr6:138953705
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0183 | 2 | NA18940.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.154-5792G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953705 | ||||||
| chr6:138953706
|
G | A | 29 | a0001c0001t0001g0194a0002c0003t0004g0016a0002c0003t0004g0017others(26): Show | 29 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-5793C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953706 | ||||||
| chr6:138953738
|
T | C | 88 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.154-5825A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953738 | ||||||
| chr6:138953846
|
T | C | 29 | a0001c0001t0001g0194a0002c0003t0004g0016a0002c0003t0004g0017others(26): Show | 29 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-5933A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953846 | ||||||
| chr6:138953993
|
C | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0156others(50): Show | 54 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.154-6080G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138953993 | ||||||
| chr6:138954317
|
T | C | 1 | a0001c0002t0003g0348 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154-6404A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138954317 | ||||||
| chr6:138954471
|
A | C | 1 | a0001c0001t0001g0296 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.154-6558T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138954471 | ||||||
| chr6:138954502
|
T | TA | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 259 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.154-6590dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138954502 | ||||||
| chr6:138954529
|
A | C | 1 | a0001c0001t0002g0057 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154-6616T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138954529 | ||||||
| chr6:138954645
|
T | C | 1 | a0001c0001t0023g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.154-6732A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138954645 | ||||||
| chr6:138954658
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.154-6745G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138954658 | ||||||
| chr6:138955119
|
T | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.154-7206A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955119 | ||||||
| chr6:138955147
|
C | T | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-7234G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955147 | ||||||
| chr6:138955295
|
T | C | 2 | a0001c0001t0002g0050a0001c0001t0002g0056 | 2 | HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.154-7382A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955295 | ||||||
| chr6:138955364
|
T | C | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.154-7451A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955364 | ||||||
| chr6:138955399
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.154-7486C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955399 | ||||||
| chr6:138955440
|
TA | T | 6 | a0001c0001t0002g0081a0001c0001t0002g0086a0001c0001t0002g0097others(3): Show | 6 | HG01256.hp1 HG01943.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-7528delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955440 | ||||||
| chr6:138955456
|
A | AGTGTGTG others(4): Show |
1 | a0001c0002t0003g0343 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.154-7544_154-7543i others(13): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955456 | ||||||
| chr6:138955457
|
A | AAAGTGTG others(5): Show |
1 | a0001c0001t0001g0221 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.154-7545_154-7544i others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAAGTGTG others(7): Show |
1 | a0001c0001t0001g0164 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.154-7545_154-7544i others(16): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAAGTGTG others(13): Show |
1 | a0001c0001t0001g0258 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.154-7545_154-7544i others(22): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGGTGTG others(11): Show |
1 | a0001c0001t0001g0243 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.154-7545_154-7544i others(20): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGT | 7 | a0001c0001t0001g0176a0001c0001t0001g0185a0001c0001t0001g0214others(4): Show | 7 | HG02258.hp2 HG02622.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-7545_154-7544i others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT | 12 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0001g0178others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-7545_154-7544i others(9): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT others(2): Show |
19 | a0001c0001t0001g0166a0001c0001t0001g0175a0001c0001t0001g0196others(16): Show | 19 | HG00621.hp1 HG01069.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.154-7545_154-7544i others(11): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT others(4): Show |
44 | a0001c0001t0001g0003a0001c0001t0001g0156a0001c0001t0001g0157others(41): Show | 45 | HG00544.hp1 HG00609.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.154-7545_154-7544i others(13): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT others(6): Show |
43 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0132others(40): Show | 43 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.154-7545_154-7544i others(15): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT others(8): Show |
36 | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0131others(33): Show | 37 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.154-7545_154-7544i others(17): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT others(10): Show |
27 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(24): Show | 27 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.154-7545_154-7544i others(19): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT others(12): Show |
10 | a0001c0001t0001g0115a0001c0001t0001g0187a0001c0001t0001g0233others(7): Show | 10 | HG00280.hp2 HG00673.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.154-7545_154-7544i others(21): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT others(14): Show |
3 | a0001c0001t0001g0110a0001c0001t0001g0274a0009c0008t0001g0138 | 3 | HG01346.hp1 HG01496.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.154-7545_154-7544i others(23): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AAGTGTGT others(16): Show |
1 | a0001c0001t0001g0228 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.154-7545_154-7544i others(25): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGT | 11 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0080others(8): Show | 11 | HG00323.hp1 HG02027.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-7546_154-7545d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGTGT | 7 | a0001c0002t0002g0120a0001c0002t0003g0356a0001c0002t0008g0119others(4): Show | 7 | HG00738.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-7548_154-7545d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGTGTGT | 16 | a0001c0002t0003g0318a0001c0002t0003g0319a0001c0002t0003g0320others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-7550_154-7545d others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGTGTGTG others(1): Show |
24 | a0001c0001t0001g0212a0001c0001t0016g0005a0001c0002t0003g0328others(21): Show | 24 | HG00423.hp2 HG00741.hp1 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-7552_154-7545d others(10): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGTGTGTG others(3): Show |
11 | a0001c0001t0001g0128a0001c0002t0003g0340a0001c0002t0003g0355others(8): Show | 11 | HG02040.hp2 HG02055.hp1 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-7554_154-7545d others(12): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGTGTGTG others(5): Show |
12 | a0001c0001t0001g0112a0001c0001t0001g0219a0001c0002t0003g0336others(9): Show | 12 | HG00438.hp1 HG01168.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-7556_154-7545d others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGTGTGTG others(7): Show |
2 | a0001c0002t0003g0378a0001c0013t0001g0130 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.154-7558_154-7545d others(16): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGTGTGTG others(9): Show |
3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0007t0001g0158 | 3 | HG01081.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.154-7560_154-7545d others(18): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | AGTGTGTG others(11): Show |
1 | a0001c0001t0001g0255 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.154-7562_154-7545d others(20): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
A | T | 7 | a0001c0001t0001g0129a0001c0001t0002g0101a0001c0002t0003g0321others(4): Show | 7 | HG03225.hp2 HG03490.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-7544T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
AG | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0302 | 4 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-7545delC | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
AGT | A | 15 | a0001c0001t0001g0301a0001c0001t0002g0068a0001c0001t0002g0069others(12): Show | 15 | HG02004.hp1 HG02165.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.154-7546_154-7545d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955457
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0022g0099a0001c0001t0023g0098 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.154-7556_154-7545d others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955457 | ||||||
| chr6:138955459
|
T | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0302 | 4 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-7546A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955459 | ||||||
| chr6:138955521
|
G | T | 1 | a0001c0001t0002g0103 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.154-7608C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955521 | ||||||
| chr6:138955916
|
A | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.154-8003T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955916 | ||||||
| chr6:138955964
|
T | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-8051A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955964 | ||||||
| chr6:138955970
|
T | C | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.154-8057A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138955970 | ||||||
| chr6:138956117
|
A | G | 2 | a0001c0001t0010g0007a0001c0001t0010g0008 | 2 | HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.154-8204T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956117 | ||||||
| chr6:138956230
|
A | G | 1 | a0001c0001t0022g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-8317T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956230 | ||||||
| chr6:138956362
|
A | G | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.154-8449T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956362 | ||||||
| chr6:138956373
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.154-8460G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956373 | ||||||
| chr6:138956536
|
G | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02735.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-8623C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956536 | ||||||
| chr6:138956561
|
C | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(83): Show | 87 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-8648G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956561 | ||||||
| chr6:138956561
|
CT | C | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.154-8649delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956561 | ||||||
| chr6:138956638
|
C | G | 1 | a0001c0001t0025g0217 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.154-8725G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956638 | ||||||
| chr6:138956658
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-8745A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956658 | ||||||
| chr6:138956746
|
C | A | 77 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(74): Show | 78 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.154-8833G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956746 | ||||||
| chr6:138956811
|
G | GA | 29 | a0001c0001t0001g0169a0001c0001t0001g0194a0001c0001t0001g0275others(26): Show | 29 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-8899dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956811 | ||||||
| chr6:138956857
|
T | C | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.154-8944A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956857 | ||||||
| chr6:138956862
|
G | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0305 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.154-8949C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956862 | ||||||
| chr6:138956966
|
T | C | 1 | a0002c0003t0004g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.154-9053A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138956966 | ||||||
| chr6:138957039
|
CA | C | 173 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(170): Show | 174 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.154-9127delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957039 | ||||||
| chr6:138957120
|
T | C | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-9207A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957120 | ||||||
| chr6:138957264
|
A | T | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.154-9351T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957264 | ||||||
| chr6:138957501
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 201 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.154-9588A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957501 | ||||||
| chr6:138957542
|
G | C | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0108others(175): Show | 180 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.154-9629C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957542 | ||||||
| chr6:138957662
|
G | A | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 322 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(319): Show |
intron_variant | MODIFIER | c.154-9749C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957662 | ||||||
| chr6:138957807
|
A | T | 1 | a0002c0003t0004g0028 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.154-9894T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957807 | ||||||
| chr6:138957953
|
T | A | 1 | a0001c0001t0002g0047 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.154-10040A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957953 | ||||||
| chr6:138957978
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.154-10065C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138957978 | ||||||
| chr6:138958149
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.154-10236G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958149 | ||||||
| chr6:138958184
|
C | G | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 317 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.154-10271G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958184 | ||||||
| chr6:138958425
|
T | C | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.154-10512A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958425 | ||||||
| chr6:138958517
|
G | GC | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 322 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(319): Show |
intron_variant | MODIFIER | c.154-10605dupG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958517 | ||||||
| chr6:138958546
|
T | C | 77 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(74): Show | 78 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.154-10633A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958546 | ||||||
| chr6:138958585
|
G | C | 2 | a0005c0005t0003g0322a0005c0005t0003g0323 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.154-10672C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958585 | ||||||
| chr6:138958639
|
T | C | 3 | a0001c0001t0001g0172a0001c0001t0019g0013a0008c0010t0001g0171 | 3 | NA18943.hp2 NA19056.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.154-10726A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958639 | ||||||
| chr6:138958639
|
T | G | 1 | a0003c0004t0003g0316 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.154-10726A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958639 | ||||||
| chr6:138958694
|
T | C | 1 | a0001c0001t0007g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.154-10781A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958694 | ||||||
| chr6:138958792
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(10): Show | 14 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.154-10879A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958792 | ||||||
| chr6:138958817
|
T | C | 29 | a0001c0001t0001g0194a0002c0003t0004g0016a0002c0003t0004g0017others(26): Show | 29 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-10904A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958817 | ||||||
| chr6:138958888
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-10975A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958888 | ||||||
| chr6:138958921
|
A | C | 1 | a0001c0001t0001g0255 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.154-11008T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958921 | ||||||
| chr6:138958963
|
C | T | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.154-11050G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138958963 | ||||||
| chr6:138959031
|
C | T | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.154-11118G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959031 | ||||||
| chr6:138959113
|
G | C | 2 | a0005c0005t0003g0322a0005c0005t0003g0323 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.154-11200C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959113 | ||||||
| chr6:138959152
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0235 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.154-11239A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959152 | ||||||
| chr6:138959231
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154-11318C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959231 | ||||||
| chr6:138959286
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.154-11373A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959286 | ||||||
| chr6:138959413
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-11500A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959413 | ||||||
| chr6:138959472
|
T | TTAATA | 318 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 322 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(319): Show |
intron_variant | MODIFIER | c.154-11564_154-1156 others(9): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959472 | ||||||
| chr6:138959516
|
T | C | 1 | a0001c0002t0017g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.154-11603A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959516 | ||||||
| chr6:138959533
|
G | A | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.154-11620C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959533 | ||||||
| chr6:138959758
|
AT | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(10): Show | 14 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.154-11846delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959758 | ||||||
| chr6:138959796
|
T | C | 1 | a0001c0002t0014g0386 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.154-11883A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959796 | ||||||
| chr6:138959839
|
T | A | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.154-11926A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959839 | ||||||
| chr6:138959874
|
T | C | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.154-11961A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959874 | ||||||
| chr6:138959910
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154-11997A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959910 | ||||||
| chr6:138959978
|
C | CATAGCTA others(1): Show |
6 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 7 | HG01106.hp2 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-12073_154-1206 others(12): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138959978 | ||||||
| chr6:138960001
|
G | A | 3 | a0003c0004t0003g0315a0003c0004t0003g0316a0003c0004t0003g0317 | 3 | HG00738.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.154-12088C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138960001 | ||||||
| chr6:138960044
|
A | C | 1 | a0001c0001t0006g0009 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.154-12131T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138960044 | ||||||
| chr6:138960294
|
T | C | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.154-12381A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138960294 | ||||||
| chr6:138960468
|
G | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-12555C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138960468 | ||||||
| chr6:138960717
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154-12804C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138960717 | ||||||
| chr6:138960784
|
C | T | 3 | a0001c0001t0002g0080a0001c0001t0002g0095a0001c0001t0002g0101 | 3 | HG03490.hp2 HG03492.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.154-12871G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138960784 | ||||||
| chr6:138960888
|
T | C | 85 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(82): Show | 86 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.154-12975A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138960888 | ||||||
| chr6:138960971
|
C | A | 18 | a0002c0003t0004g0026a0002c0003t0004g0027a0002c0003t0004g0028others(15): Show | 18 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.154-13058G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138960971 | ||||||
| chr6:138961030
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.154-13117A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961030 | ||||||
| chr6:138961275
|
C | T | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.154-13362G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961275 | ||||||
| chr6:138961394
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-13481C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961394 | ||||||
| chr6:138961400
|
C | T | 1 | a0002c0003t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-13487G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961400 | ||||||
| chr6:138961403
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.154-13490T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961403 | ||||||
| chr6:138961423
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.154-13510C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961423 | ||||||
| chr6:138961440
|
T | C | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-13527A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961440 | ||||||
| chr6:138961485
|
G | A | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 317 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.154-13572C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961485 | ||||||
| chr6:138961511
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-13598A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961511 | ||||||
| chr6:138961607
|
G | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0156others(47): Show | 51 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.154-13694C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961607 | ||||||
| chr6:138961655
|
G | A | 1 | a0001c0001t0001g0003 | 2 | NA18973.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.154-13742C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961655 | ||||||
| chr6:138961680
|
G | C | 1 | a0001c0001t0002g0104 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.154-13767C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138961680 | ||||||
| chr6:138962000
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.154-14087T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138962000 | ||||||
| chr6:138962280
|
C | T | 8 | a0001c0001t0001g0141a0001c0001t0001g0156a0001c0001t0001g0172others(5): Show | 8 | NA18943.hp2 NA18959.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-14367G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138962280 | ||||||
| chr6:138962321
|
T | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.154-14408A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138962321 | ||||||
| chr6:138962562
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.154-14649A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138962562 | ||||||
| chr6:138962678
|
C | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-14765G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138962678 | ||||||
| chr6:138963062
|
A | G | 2 | a0001c0001t0002g0078a0001c0001t0002g0090 | 2 | NA19000.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.154-15149T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963062 | ||||||
| chr6:138963084
|
G | C | 1 | a0001c0002t0014g0385 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.154-15171C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963084 | ||||||
| chr6:138963111
|
ATAAC | A | 73 | a0001c0001t0001g0163a0001c0001t0001g0188a0001c0001t0001g0189others(70): Show | 73 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.154-15202_154-1519 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963111 | ||||||
| chr6:138963131
|
CTAAA | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 244 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.154-15222_154-1521 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963131 | ||||||
| chr6:138963139
|
A | C | 1 | a0002c0003t0004g0017 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.154-15226T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963139 | ||||||
| chr6:138963332
|
G | A | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG01943.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.154-15419C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963332 | ||||||
| chr6:138963360
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-15447A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963360 | ||||||
| chr6:138963363
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-15450C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963363 | ||||||
| chr6:138963429
|
G | T | 1 | a0001c0001t0009g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.154-15516C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963429 | ||||||
| chr6:138963447
|
T | C | 1 | a0001c0002t0003g0360 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.154-15534A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963447 | ||||||
| chr6:138963730
|
C | A | 115 | a0001c0001t0002g0072a0001c0001t0003g0324a0001c0002t0002g0001others(112): Show | 116 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(113): Show |
intron_variant | MODIFIER | c.154-15817G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963730 | ||||||
| chr6:138963793
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-15880T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963793 | ||||||
| chr6:138963820
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.154-15907A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963820 | ||||||
| chr6:138963918
|
A | G | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.154-16005T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138963918 | ||||||
| chr6:138964136
|
A | G | 1 | a0002c0003t0004g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.154-16223T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964136 | ||||||
| chr6:138964189
|
T | C | 79 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(76): Show | 79 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.154-16276A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964189 | ||||||
| chr6:138964224
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0305 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.154-16311G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964224 | ||||||
| chr6:138964339
|
T | C | 15 | a0002c0003t0004g0026a0002c0003t0004g0027a0002c0003t0004g0028others(12): Show | 15 | HG01069.hp1 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.154-16426A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964339 | ||||||
| chr6:138964493
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 202 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.154-16580C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964493 | ||||||
| chr6:138964495
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-16582T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964495 | ||||||
| chr6:138964567
|
C | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 202 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.154-16654G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964567 | ||||||
| chr6:138964571
|
A | T | 2 | a0001c0002t0008g0117a0001c0002t0008g0119 | 2 | NA18940.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.154-16658T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964571 | ||||||
| chr6:138964666
|
C | T | 2 | a0001c0001t0022g0099a0001c0001t0023g0098 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.154-16753G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964666 | ||||||
| chr6:138964844
|
C | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-16931G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964844 | ||||||
| chr6:138964935
|
T | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-17022A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964935 | ||||||
| chr6:138964959
|
C | T | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.154-17046G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964959 | ||||||
| chr6:138964962
|
C | G | 3 | a0001c0001t0001g0172a0001c0001t0019g0013a0008c0010t0001g0171 | 3 | NA18943.hp2 NA19056.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.154-17049G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964962 | ||||||
| chr6:138964982
|
C | A | 2 | a0001c0001t0022g0099a0001c0001t0023g0098 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.154-17069G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138964982 | ||||||
| chr6:138965497
|
G | T | 1 | a0001c0002t0008g0119 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.154-17584C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965497 | ||||||
| chr6:138965500
|
A | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 316 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(313): Show |
intron_variant | MODIFIER | c.154-17587T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965500 | ||||||
| chr6:138965504
|
T | C | 1 | a0001c0002t0008g0119 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.154-17591A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965504 | ||||||
| chr6:138965507
|
G | A | 1 | a0001c0002t0008g0119 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.154-17594C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965507 | ||||||
| chr6:138965509
|
A | T | 1 | a0001c0002t0008g0119 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.154-17596T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965509 | ||||||
| chr6:138965513
|
A | G | 1 | a0001c0002t0008g0119 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.154-17600T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965513 | ||||||
| chr6:138965514
|
G | T | 1 | a0001c0002t0008g0119 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.154-17601C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965514 | ||||||
| chr6:138965542
|
G | A | 1 | a0004c0006t0001g0290 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.154-17629C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965542 | ||||||
| chr6:138965560
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.154-17647A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965560 | ||||||
| chr6:138965587
|
T | C | 3 | a0001c0001t0003g0324a0005c0005t0003g0322a0005c0005t0003g0323 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.154-17674A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965587 | ||||||
| chr6:138965623
|
A | G | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-17710T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965623 | ||||||
| chr6:138965720
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.154-17807C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965720 | ||||||
| chr6:138965840
|
C | G | 1 | a0001c0002t0003g0377 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.154-17927G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965840 | ||||||
| chr6:138965915
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.154-18002T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138965915 | ||||||
| chr6:138966122
|
A | G | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.154-18209T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966122 | ||||||
| chr6:138966275
|
TTAC | T | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-18365_154-1836 others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966275 | ||||||
| chr6:138966434
|
A | G | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-18521T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966434 | ||||||
| chr6:138966535
|
T | C | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.154-18622A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966535 | ||||||
| chr6:138966563
|
T | G | 3 | a0003c0004t0003g0315a0003c0004t0003g0316a0003c0004t0003g0317 | 3 | HG00738.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.154-18650A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966563 | ||||||
| chr6:138966711
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.154-18798C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966711 | ||||||
| chr6:138966788
|
AAAAAG | A | 79 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(76): Show | 80 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.154-18880_154-1887 others(9): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966788 | ||||||
| chr6:138966801
|
T | G | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.154-18888A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966801 | ||||||
| chr6:138966862
|
T | A | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 318 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.154-18949A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966862 | ||||||
| chr6:138966995
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(8): Show | 12 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-19082C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138966995 | ||||||
| chr6:138967007
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.154-19094G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967007 | ||||||
| chr6:138967049
|
T | C | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0289 | 3 | HG02723.hp1 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.154-19136A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967049 | ||||||
| chr6:138967112
|
G | A | 17 | a0001c0002t0003g0318a0001c0002t0003g0319a0001c0002t0003g0320others(14): Show | 17 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.154-19199C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967112 | ||||||
| chr6:138967262
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.154-19349G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967262 | ||||||
| chr6:138967283
|
A | G | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.154-19370T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967283 | ||||||
| chr6:138967485
|
G | C | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.154-19572C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967485 | ||||||
| chr6:138967515
|
G | A | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.154-19602C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967515 | ||||||
| chr6:138967642
|
T | C | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-19729A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967642 | ||||||
| chr6:138967704
|
T | G | 3 | a0001c0001t0001g0264a0001c0001t0001g0274a0001c0001t0001g0286 | 3 | NA18981.hp1 NA19009.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.154-19791A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967704 | ||||||
| chr6:138967787
|
T | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 318 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.153+19743A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967787 | ||||||
| chr6:138967827
|
C | A | 88 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.153+19703G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967827 | ||||||
| chr6:138967924
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02074.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.153+19606T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967924 | ||||||
| chr6:138967976
|
C | T | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG00733.hp1 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+19554G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967976 | ||||||
| chr6:138967986
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+19544G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967986 | ||||||
| chr6:138967987
|
G | T | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153+19543C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138967987 | ||||||
| chr6:138968042
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.153+19488C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968042 | ||||||
| chr6:138968315
|
T | C | 90 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(87): Show | 90 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.153+19215A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968315 | ||||||
| chr6:138968510
|
TC | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+19019delG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968510 | ||||||
| chr6:138968754
|
C | T | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.153+18776G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968754 | ||||||
| chr6:138968766
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.153+18764G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968766 | ||||||
| chr6:138968852
|
A | T | 2 | a0001c0002t0003g0321a0001c0002t0003g0374 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.153+18678T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968852 | ||||||
| chr6:138968878
|
T | C | 2 | a0002c0003t0012g0307a0002c0003t0012g0308 | 2 | HG01069.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.153+18652A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968878 | ||||||
| chr6:138968905
|
CA | C | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.153+18624delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968905 | ||||||
| chr6:138968913
|
AAG | A | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+18615_153+1861 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138968913 | ||||||
| chr6:138969269
|
A | AT | 23 | a0001c0001t0001g0140a0001c0001t0001g0224a0001c0001t0002g0042others(20): Show | 23 | HG00733.hp2 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.153+18260dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATT | 67 | a0001c0001t0001g0139a0001c0001t0001g0149a0001c0001t0001g0150others(64): Show | 67 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.153+18259_153+1826 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTT | 21 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0156others(18): Show | 22 | HG00609.hp1 HG00621.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.153+18258_153+1826 others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTT | 8 | a0001c0001t0001g0002a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 9 | HG01106.hp2 HG01243.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+18257_153+1826 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTT | 7 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0137others(4): Show | 7 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+18256_153+1826 others(9): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0009g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+18250_153+1826 others(15): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0009g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.153+18249_153+1826 others(16): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(6): Show |
16 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0153others(13): Show | 16 | HG02015.hp1 HG02074.hp1 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.153+18248_153+1826 others(17): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(7): Show |
14 | a0001c0001t0001g0125a0001c0001t0001g0236a0001c0001t0001g0243others(11): Show | 14 | HG00609.hp2 HG02129.hp2 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.153+18247_153+1826 others(18): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(8): Show |
13 | a0001c0001t0001g0245a0001c0001t0001g0248a0001c0001t0001g0249others(10): Show | 13 | HG00423.hp1 HG00438.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+18246_153+1826 others(19): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(9): Show |
3 | a0001c0001t0001g0231a0001c0001t0001g0295a0011c0014t0001g0271 | 3 | NA18979.hp2 NA18995.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.153+18245_153+1826 others(20): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(10): Show |
3 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0242 | 3 | HG02698.hp1 HG04199.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.153+18244_153+1826 others(21): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(11): Show |
7 | a0001c0001t0001g0228a0001c0001t0001g0232a0001c0001t0001g0238others(4): Show | 7 | HG03453.hp2 NA18944.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+18243_153+1826 others(22): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0256a0001c0001t0001g0270 | 2 | HG00597.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.153+18242_153+1826 others(23): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(13): Show |
4 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0114others(1): Show | 4 | HG01943.hp1 HG01993.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+18241_153+1826 others(24): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(14): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0115a0001c0001t0001g0151others(1): Show | 4 | HG00280.hp2 HG00733.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+18240_153+1826 others(25): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(15): Show |
3 | a0001c0001t0001g0131a0001c0001t0001g0152a0001c0001t0001g0237 | 3 | HG01516.hp1 HG03098.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.153+18239_153+1826 others(26): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(19): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0292 | 3 | HG00558.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.153+18235_153+1826 others(30): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
A | ATTTTTTT others(24): Show |
2 | a0001c0001t0001g0109a0001c0001t0029g0382 | 2 | HG00323.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.153+18260_153+1826 others(35): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
AT | A | 9 | a0001c0001t0001g0129a0001c0001t0001g0304a0001c0001t0002g0057others(6): Show | 9 | HG00544.hp2 HG00639.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+18260delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
ATTTTTT | A | 26 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(23): Show | 26 | HG01069.hp1 HG01433.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.153+18255_153+1826 others(10): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
ATTTTTTT | A | 7 | a0001c0001t0001g0155a0001c0002t0003g0332a0001c0002t0003g0343others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+18254_153+1826 others(11): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
ATTTTTTT others(1): Show |
A | 73 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.153+18253_153+1826 others(12): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969269
|
ATTTTTTT others(3): Show |
A | 8 | a0001c0001t0001g0004a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+18251_153+1826 others(14): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969269 | ||||||
| chr6:138969360
|
C | T | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.153+18170G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969360 | ||||||
| chr6:138969451
|
A | AT | 103 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0002g0001others(100): Show | 104 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(101): Show |
intron_variant | MODIFIER | c.153+18078dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969451 | ||||||
| chr6:138969583
|
C | T | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153+17947G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969583 | ||||||
| chr6:138969737
|
T | A | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+17793A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969737 | ||||||
| chr6:138969777
|
G | A | 2 | a0001c0001t0002g0060a0010c0012t0002g0061 | 2 | HG00738.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.153+17753C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969777 | ||||||
| chr6:138969832
|
TAAAG | T | 11 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(8): Show | 12 | HG02027.hp1 HG03704.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+17694_153+1769 others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969832 | ||||||
| chr6:138969859
|
A | ATT | 67 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0156others(64): Show | 67 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.153+17669_153+1767 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969859 | ||||||
| chr6:138969859
|
A | ATTT | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 36 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.153+17668_153+1767 others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969859 | ||||||
| chr6:138969859
|
A | ATTTTTT | 58 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(55): Show | 58 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.153+17665_153+1767 others(10): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969859 | ||||||
| chr6:138969859
|
A | ATTTTTTT | 27 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.153+17664_153+1767 others(11): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969859 | ||||||
| chr6:138969859
|
A | ATTTTTTT others(1): Show |
6 | a0001c0001t0001g0108a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG00438.hp2 HG02735.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+17663_153+1767 others(12): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969859 | ||||||
| chr6:138969859
|
AT | A | 29 | a0001c0001t0002g0293a0001c0001t0006g0009a0001c0001t0006g0010others(26): Show | 29 | HG00323.hp1 HG00423.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.153+17670delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969859 | ||||||
| chr6:138969859
|
ATT | A | 81 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0120others(78): Show | 82 | HG00438.hp1 HG00741.hp1 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.153+17669_153+1767 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969859 | ||||||
| chr6:138969884
|
T | A | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.153+17646A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969884 | ||||||
| chr6:138969885
|
A | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+17645T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969885 | ||||||
| chr6:138969930
|
G | A | 1 | a0001c0013t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.153+17600C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969930 | ||||||
| chr6:138969964
|
G | T | 80 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(77): Show | 81 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.153+17566C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138969964 | ||||||
| chr6:138970151
|
G | A | 1 | a0001c0002t0003g0374 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.153+17379C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970151 | ||||||
| chr6:138970163
|
G | A | 1 | a0004c0006t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153+17367C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970163 | ||||||
| chr6:138970300
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+17230A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970300 | ||||||
| chr6:138970433
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.153+17097A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970433 | ||||||
| chr6:138970457
|
T | TA | 278 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(275): Show | 282 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.153+17072dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970457 | ||||||
| chr6:138970457
|
T | TAA | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0019others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+17071_153+1707 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970457 | ||||||
| chr6:138970504
|
G | A | 2 | a0001c0002t0003g0321a0001c0002t0003g0374 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.153+17026C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970504 | ||||||
| chr6:138970603
|
G | A | 1 | a0001c0001t0026g0306 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.153+16927C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970603 | ||||||
| chr6:138970640
|
C | T | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.153+16890G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970640 | ||||||
| chr6:138970672
|
T | A | 1 | a0001c0002t0003g0362 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.153+16858A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970672 | ||||||
| chr6:138970918
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.153+16612A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970918 | ||||||
| chr6:138970932
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+16598T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138970932 | ||||||
| chr6:138971019
|
C | T | 1 | a0001c0002t0003g0366 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.153+16511G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971019 | ||||||
| chr6:138971249
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.153+16281A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971249 | ||||||
| chr6:138971251
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.153+16279T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971251 | ||||||
| chr6:138971296
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+16234G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971296 | ||||||
| chr6:138971445
|
T | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+16085A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971445 | ||||||
| chr6:138971472
|
G | GA | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+16057dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971472 | ||||||
| chr6:138971521
|
A | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+16009T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971521 | ||||||
| chr6:138971546
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 203 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.153+15984T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971546 | ||||||
| chr6:138971590
|
T | TA | 81 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(78): Show | 82 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.153+15939dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971590 | ||||||
| chr6:138971640
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.153+15890C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971640 | ||||||
| chr6:138971856
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+15674A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971856 | ||||||
| chr6:138971878
|
G | A | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153+15652C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971878 | ||||||
| chr6:138971972
|
C | A | 88 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.153+15558G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138971972 | ||||||
| chr6:138972322
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.153+15208C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138972322 | ||||||
| chr6:138972435
|
G | C | 1 | a0001c0001t0016g0005 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.153+15095C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138972435 | ||||||
| chr6:138972498
|
C | T | 1 | a0001c0002t0003g0372 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.153+15032G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138972498 | ||||||
| chr6:138972670
|
C | T | 1 | a0001c0002t0003g0371 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.153+14860G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138972670 | ||||||
| chr6:138972683
|
T | TA | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.153+14846dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138972683 | ||||||
| chr6:138972683
|
TA | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.153+14846delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138972683 | ||||||
| chr6:138972683
|
TAA | T | 10 | a0001c0001t0001g0112a0001c0001t0001g0143a0001c0001t0001g0147others(7): Show | 10 | HG00558.hp2 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+14845_153+1484 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138972683 | ||||||
| chr6:138972732
|
G | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+14798C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138972732 | ||||||
| chr6:138973004
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+14526G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973004 | ||||||
| chr6:138973012
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.153+14518C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973012 | ||||||
| chr6:138973055
|
C | G | 88 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.153+14475G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973055 | ||||||
| chr6:138973064
|
T | G | 354 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(351): Show | 358 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(355): Show |
intron_variant | MODIFIER | c.153+14466A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973064 | ||||||
| chr6:138973392
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+14138C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973392 | ||||||
| chr6:138973437
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.153+14093G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973437 | ||||||
| chr6:138973506
|
T | A | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153+14024A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973506 | ||||||
| chr6:138973568
|
G | T | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 318 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.153+13962C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973568 | ||||||
| chr6:138973582
|
T | TCTGACTT others(316): Show |
18 | a0002c0003t0004g0019a0002c0003t0004g0020a0002c0003t0004g0021others(15): Show | 18 | HG01069.hp1 HG01433.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.153+13947_153+1394 others(327): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973582 | ||||||
| chr6:138973582
|
T | TCTGACTT others(316): Show |
1 | a0002c0003t0004g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.153+13947_153+1394 others(327): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973582 | ||||||
| chr6:138973582
|
T | TCTGACTT others(317): Show |
7 | a0002c0003t0004g0017a0002c0003t0004g0018a0002c0003t0004g0026others(4): Show | 7 | HG02257.hp1 HG02258.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+13947_153+1394 others(328): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973582 | ||||||
| chr6:138973582
|
T | TCTGACTT others(318): Show |
2 | a0002c0003t0004g0016a0002c0003t0004g0037 | 2 | HG01192.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.153+13947_153+1394 others(329): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973582 | ||||||
| chr6:138973650
|
T | A | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.153+13880A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973650 | ||||||
| chr6:138973661
|
T | C | 114 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.153+13869A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138973661 | ||||||
| chr6:138974294
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+13236C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138974294 | ||||||
| chr6:138974457
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.153+13073G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138974457 | ||||||
| chr6:138974593
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+12937G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138974593 | ||||||
| chr6:138974728
|
T | C | 3 | a0001c0001t0002g0080a0001c0001t0002g0095a0001c0001t0002g0101 | 3 | HG03490.hp2 HG03492.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.153+12802A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138974728 | ||||||
| chr6:138974773
|
C | T | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153+12757G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138974773 | ||||||
| chr6:138974785
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.153+12745G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138974785 | ||||||
| chr6:138974851
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+12679T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138974851 | ||||||
| chr6:138974881
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+12649G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138974881 | ||||||
| chr6:138975184
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+12346T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975184 | ||||||
| chr6:138975199
|
A | C | 1 | a0001c0001t0016g0005 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.153+12331T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975199 | ||||||
| chr6:138975234
|
C | T | 2 | a0001c0001t0022g0099a0001c0001t0023g0098 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.153+12296G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975234 | ||||||
| chr6:138975297
|
C | G | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 317 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.153+12233G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975297 | ||||||
| chr6:138975320
|
A | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+12210T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975320 | ||||||
| chr6:138975380
|
G | A | 1 | a0001c0002t0003g0350 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.153+12150C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975380 | ||||||
| chr6:138975657
|
A | C | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.153+11873T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975657 | ||||||
| chr6:138975798
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0187 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.153+11732G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975798 | ||||||
| chr6:138975807
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+11723G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975807 | ||||||
| chr6:138975948
|
T | C | 1 | a0001c0001t0002g0293 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153+11582A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138975948 | ||||||
| chr6:138976116
|
C | T | 1 | a0001c0002t0003g0366 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.153+11414G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976116 | ||||||
| chr6:138976250
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0261 | 2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.153+11280G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976250 | ||||||
| chr6:138976312
|
T | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+11218A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976312 | ||||||
| chr6:138976320
|
C | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+11210G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976320 | ||||||
| chr6:138976376
|
A | T | 1 | a0001c0001t0002g0076 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.153+11154T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976376 | ||||||
| chr6:138976408
|
A | T | 60 | a0001c0002t0003g0318a0001c0002t0003g0319a0001c0002t0003g0320others(57): Show | 60 | HG00423.hp2 HG00438.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.153+11122T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976408 | ||||||
| chr6:138976473
|
C | T | 1 | a0001c0007t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153+11057G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976473 | ||||||
| chr6:138976474
|
G | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+11056C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976474 | ||||||
| chr6:138976920
|
A | C | 1 | a0001c0007t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153+10610T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138976920 | ||||||
| chr6:138977050
|
A | T | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+10480T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138977050 | ||||||
| chr6:138977365
|
GCT | G | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+10163_153+1016 others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138977365 | ||||||
| chr6:138977504
|
A | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+10026T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138977504 | ||||||
| chr6:138977599
|
TTC | T | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+9929_153+9930d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138977599 | ||||||
| chr6:138977687
|
T | C | 2 | a0001c0002t0014g0385a0001c0002t0014g0386 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.153+9843A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138977687 | ||||||
| chr6:138977875
|
G | A | 3 | a0001c0002t0003g0352a0001c0002t0003g0353a0001c0002t0028g0351 | 3 | HG02895.hp1 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.153+9655C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138977875 | ||||||
| chr6:138978085
|
C | T | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+9445G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978085 | ||||||
| chr6:138978095
|
G | GT | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(268): Show | 275 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.153+9434dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978095 | ||||||
| chr6:138978095
|
G | GTT | 7 | a0001c0001t0001g0214a0001c0001t0001g0220a0001c0001t0001g0250others(4): Show | 7 | HG02647.hp1 HG03942.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+9433_153+9434d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978095 | ||||||
| chr6:138978107
|
T | TA | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+9422_153+9423i others(3): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978107 | ||||||
| chr6:138978108
|
C | A | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+9422G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978108 | ||||||
| chr6:138978282
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+9248G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978282 | ||||||
| chr6:138978286
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.153+9244A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978286 | ||||||
| chr6:138978293
|
C | CT | 83 | a0001c0001t0001g0148a0001c0001t0001g0261a0001c0001t0013g0380others(80): Show | 84 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.153+9236dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978293 | ||||||
| chr6:138978314
|
G | T | 1 | a0002c0003t0004g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.153+9216C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978314 | ||||||
| chr6:138978323
|
C | A | 82 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(79): Show | 83 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.153+9207G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978323 | ||||||
| chr6:138978365
|
TCTGACCT others(8): Show |
T | 13 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(10): Show | 14 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.153+9150_153+9164d others(17): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978365 | ||||||
| chr6:138978450
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.153+9080G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978450 | ||||||
| chr6:138978481
|
C | CT | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0108others(137): Show | 142 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.153+9048dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978481 | ||||||
| chr6:138978481
|
C | CTT | 87 | a0001c0001t0001g0129a0001c0001t0003g0324a0001c0002t0002g0001others(84): Show | 88 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.153+9047_153+9048d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978481 | ||||||
| chr6:138978570
|
A | G | 1 | a0001c0002t0002g0116 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.153+8960T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978570 | ||||||
| chr6:138978590
|
A | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01192.hp2 HG01255.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+8940T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978590 | ||||||
| chr6:138978701
|
G | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0289 | 3 | HG02723.hp1 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.153+8829C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978701 | ||||||
| chr6:138978820
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.153+8710T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138978820 | ||||||
| chr6:138979095
|
C | T | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.153+8435G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979095 | ||||||
| chr6:138979180
|
C | CA | 71 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0131others(68): Show | 71 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.153+8349dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979180 | ||||||
| chr6:138979180
|
C | CAA | 86 | a0001c0001t0001g0003a0001c0001t0001g0108a0001c0001t0001g0109others(83): Show | 87 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+8348_153+8349d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979180 | ||||||
| chr6:138979180
|
C | CAAA | 27 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(24): Show | 27 | HG00280.hp2 HG00544.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.153+8347_153+8349d others(5): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979180 | ||||||
| chr6:138979180
|
C | CAAAAAA | 11 | a0001c0001t0001g0145a0002c0003t0004g0019a0002c0003t0004g0020others(8): Show | 11 | HG01069.hp1 HG01433.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+8344_153+8349d others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979180 | ||||||
| chr6:138979193
|
AAAAAC | A | 48 | a0001c0002t0003g0318a0001c0002t0003g0319a0001c0002t0003g0325others(45): Show | 48 | HG00423.hp2 HG01891.hp1 HG02040.hp2 others(45): Show |
intron_variant | MODIFIER | c.153+8332_153+8336d others(7): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979193 | ||||||
| chr6:138979194
|
AAAAC | A | 29 | a0001c0002t0002g0001a0001c0002t0002g0118a0001c0002t0002g0120others(26): Show | 30 | HG00438.hp1 HG00741.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.153+8332_153+8335d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979194 | ||||||
| chr6:138979195
|
AAAC | A | 10 | a0001c0001t0003g0324a0001c0002t0002g0116a0001c0002t0002g0123others(7): Show | 10 | HG00738.hp2 HG02027.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+8332_153+8334d others(5): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979195 | ||||||
| chr6:138979198
|
C | A | 43 | a0001c0001t0001g0115a0001c0001t0001g0142a0001c0001t0001g0143others(40): Show | 43 | HG00280.hp2 HG00423.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.153+8332G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979198 | ||||||
| chr6:138979251
|
T | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+8279A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979251 | ||||||
| chr6:138979379
|
T | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(8): Show | 12 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+8151A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979379 | ||||||
| chr6:138979425
|
T | C | 4 | a0001c0002t0003g0337a0001c0002t0003g0363a0001c0002t0003g0364others(1): Show | 4 | NA18979.hp1 NA18981.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+8105A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979425 | ||||||
| chr6:138979460
|
G | C | 1 | a0001c0002t0003g0374 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.153+8070C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979460 | ||||||
| chr6:138979525
|
T | G | 1 | a0001c0001t0002g0293 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153+8005A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979525 | ||||||
| chr6:138979656
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.153+7874A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979656 | ||||||
| chr6:138979717
|
A | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02735.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+7813T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979717 | ||||||
| chr6:138979739
|
C | T | 8 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(5): Show | 8 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+7791G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979739 | ||||||
| chr6:138979740
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(2): Show | 6 | HG01884.hp2 HG01978.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+7790C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979740 | ||||||
| chr6:138979815
|
C | G | 5 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+7715G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979815 | ||||||
| chr6:138979877
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.153+7653C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979877 | ||||||
| chr6:138979986
|
A | C | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153+7544T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138979986 | ||||||
| chr6:138980040
|
C | T | 75 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(72): Show | 75 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.153+7490G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980040 | ||||||
| chr6:138980111
|
C | T | 1 | a0002c0003t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.153+7419G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980111 | ||||||
| chr6:138980140
|
T | C | 1 | a0001c0002t0003g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.153+7390A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980140 | ||||||
| chr6:138980356
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.153+7174G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980356 | ||||||
| chr6:138980418
|
C | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+7112G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980418 | ||||||
| chr6:138980549
|
A | AC | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+6980dupG | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980549 | ||||||
| chr6:138980636
|
C | A | 40 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0244others(37): Show | 40 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.153+6894G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980636 | ||||||
| chr6:138980664
|
CT | C | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+6865delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980664 | ||||||
| chr6:138980685
|
C | CG | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0125others(147): Show | 152 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.153+6844dupC | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980685 | ||||||
| chr6:138980685
|
C | CGG | 53 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0132others(50): Show | 53 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.153+6843_153+6844d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980685 | ||||||
| chr6:138980685
|
CG | C | 29 | a0001c0001t0001g0143a0001c0001t0001g0197a0001c0001t0001g0276others(26): Show | 29 | HG00423.hp2 HG02027.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.153+6844delC | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980685 | ||||||
| chr6:138980685
|
CGG | C | 54 | a0001c0002t0002g0001a0001c0002t0002g0118a0001c0002t0002g0120others(51): Show | 55 | HG00438.hp1 HG00741.hp1 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.153+6843_153+6844d others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980685 | ||||||
| chr6:138980694
|
G | C | 9 | a0001c0002t0003g0366a0001c0002t0003g0367a0001c0002t0003g0368others(6): Show | 9 | HG00438.hp1 HG02040.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+6836C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980694 | ||||||
| chr6:138980699
|
A | G | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+6831T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980699 | ||||||
| chr6:138980844
|
C | T | 90 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(87): Show | 91 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+6686G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980844 | ||||||
| chr6:138980941
|
C | A | 3 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018 | 3 | HG02258.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.153+6589G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138980941 | ||||||
| chr6:138981027
|
A | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 202 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.153+6503T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981027 | ||||||
| chr6:138981050
|
A | G | 4 | a0001c0002t0014g0385a0001c0002t0014g0386a0001c0002t0015g0383others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+6480T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981050 | ||||||
| chr6:138981079
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.153+6451C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981079 | ||||||
| chr6:138981278
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.153+6252A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981278 | ||||||
| chr6:138981368
|
TACAC | T | 6 | a0001c0002t0003g0318a0001c0002t0003g0325a0001c0002t0003g0327others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+6158_153+6161d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981368 | ||||||
| chr6:138981451
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.153+6079C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981451 | ||||||
| chr6:138981479
|
A | C | 60 | a0001c0002t0003g0318a0001c0002t0003g0319a0001c0002t0003g0320others(57): Show | 60 | HG00423.hp2 HG00438.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.153+6051T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981479 | ||||||
| chr6:138981615
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+5915G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981615 | ||||||
| chr6:138981619
|
C | A | 33 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0199others(30): Show | 33 | HG00639.hp2 HG01074.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.153+5911G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981619 | ||||||
| chr6:138981758
|
G | A | 5 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+5772C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981758 | ||||||
| chr6:138981809
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153+5721G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981809 | ||||||
| chr6:138981898
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153+5632A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981898 | ||||||
| chr6:138981904
|
AAAAC | A | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+5622_153+5625d others(6): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981904 | ||||||
| chr6:138981966
|
A | AT | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG00733.hp1 HG01109.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+5563dupA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138981966 | ||||||
| chr6:138982004
|
T | C | 75 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(72): Show | 75 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.153+5526A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982004 | ||||||
| chr6:138982146
|
A | T | 3 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018 | 3 | HG02258.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.153+5384T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982146 | ||||||
| chr6:138982219
|
G | T | 1 | a0001c0002t0003g0326 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.153+5311C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982219 | ||||||
| chr6:138982283
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153+5247G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982283 | ||||||
| chr6:138982340
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.153+5190G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982340 | ||||||
| chr6:138982372
|
A | G | 2 | a0005c0005t0003g0322a0005c0005t0003g0323 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.153+5158T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982372 | ||||||
| chr6:138982473
|
C | T | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0011 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.153+5057G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982473 | ||||||
| chr6:138982595
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+4935T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982595 | ||||||
| chr6:138982792
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.153+4738G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982792 | ||||||
| chr6:138982928
|
T | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 202 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.153+4602A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982928 | ||||||
| chr6:138982943
|
C | T | 2 | a0001c0001t0001g0139a0009c0008t0001g0138 | 2 | HG00639.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.153+4587G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138982943 | ||||||
| chr6:138983111
|
T | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | NA19060.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.153+4419A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983111 | ||||||
| chr6:138983115
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+4415T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983115 | ||||||
| chr6:138983117
|
T | C | 6 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(3): Show | 6 | HG02040.hp1 HG02129.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+4413A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983117 | ||||||
| chr6:138983257
|
G | T | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153+4273C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983257 | ||||||
| chr6:138983281
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+4249C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983281 | ||||||
| chr6:138983324
|
G | A | 2 | a0001c0001t0001g0129a0001c0013t0001g0130 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.153+4206C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983324 | ||||||
| chr6:138983455
|
AAAAAAT | A | 78 | a0001c0002t0002g0001a0001c0002t0002g0116a0001c0002t0002g0118others(75): Show | 79 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.153+4069_153+4074d others(8): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983455 | ||||||
| chr6:138983482
|
A | T | 1 | a0001c0002t0003g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.153+4048T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983482 | ||||||
| chr6:138983526
|
G | T | 1 | a0001c0001t0016g0005 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.153+4004C>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983526 | ||||||
| chr6:138983631
|
C | T | 1 | a0001c0002t0003g0326 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.153+3899G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983631 | ||||||
| chr6:138983850
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(5): Show | 9 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+3680G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983850 | ||||||
| chr6:138983907
|
C | A | 1 | a0001c0001t0001g0286 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.153+3623G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138983907 | ||||||
| chr6:138984074
|
C | A | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+3456G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984074 | ||||||
| chr6:138984078
|
CT | C | 83 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(80): Show | 84 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.153+3451delA | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984078 | ||||||
| chr6:138984080
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0002g0102 | 2 | HG00558.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.153+3450A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984080 | ||||||
| chr6:138984122
|
T | C | 1 | a0004c0006t0001g0290 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.153+3408A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984122 | ||||||
| chr6:138984232
|
C | T | 2 | a0001c0002t0003g0319a0001c0002t0003g0320 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.153+3298G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984232 | ||||||
| chr6:138984247
|
C | A | 2 | a0001c0002t0003g0376a0001c0002t0003g0377 | 2 | HG00423.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.153+3283G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984247 | ||||||
| chr6:138984268
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153+3262T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984268 | ||||||
| chr6:138984272
|
A | C | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+3258T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984272 | ||||||
| chr6:138984491
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.153+3039C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984491 | ||||||
| chr6:138984575
|
C | CA | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+2954dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984575 | ||||||
| chr6:138984614
|
T | C | 1 | a0003c0004t0003g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.153+2916A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984614 | ||||||
| chr6:138984712
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153+2818G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984712 | ||||||
| chr6:138984802
|
A | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0013t0001g0130 | 3 | HG02055.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.153+2728T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984802 | ||||||
| chr6:138984827
|
C | A | 2 | a0001c0001t0001g0292a0001c0001t0029g0382 | 2 | HG00558.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.153+2703G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984827 | ||||||
| chr6:138984838
|
T | G | 1 | a0002c0003t0012g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153+2692A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984838 | ||||||
| chr6:138984888
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.153+2642T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138984888 | ||||||
| chr6:138985047
|
T | C | 2 | a0001c0002t0015g0383a0001c0002t0015g0384 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153+2483A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138985047 | ||||||
| chr6:138985120
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+2410T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138985120 | ||||||
| chr6:138985153
|
A | T | 1 | a0001c0002t0003g0318 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.153+2377T>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138985153 | ||||||
| chr6:138985174
|
C | T | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 315 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(312): Show |
intron_variant | MODIFIER | c.153+2356G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138985174 | ||||||
| chr6:138985256
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153+2274G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138985256 | ||||||
| chr6:138985604
|
C | T | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+1926G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138985604 | ||||||
| chr6:138985784
|
A | C | 3 | a0003c0004t0003g0315a0003c0004t0003g0316a0003c0004t0003g0317 | 3 | HG00738.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.153+1746T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138985784 | ||||||
| chr6:138985814
|
T | C | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+1716A>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138985814 | ||||||
| chr6:138986126
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+1404G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986126 | ||||||
| chr6:138986295
|
A | G | 7 | a0002c0003t0004g0019a0002c0003t0004g0020a0002c0003t0004g0021others(4): Show | 7 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+1235T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986295 | ||||||
| chr6:138986340
|
G | A | 4 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0105others(1): Show | 4 | HG01099.hp1 HG01168.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+1190C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986340 | ||||||
| chr6:138986386
|
A | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+1144T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986386 | ||||||
| chr6:138986497
|
T | TAC | 5 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297others(2): Show | 5 | HG00609.hp2 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+1032_153+1033i others(4): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986497 | ||||||
| chr6:138986516
|
C | A | 2 | a0001c0002t0003g0378a0001c0002t0003g0379 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.153+1014G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986516 | ||||||
| chr6:138986516
|
C | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | NA19060.hp2 NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.153+1014G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986516 | ||||||
| chr6:138986538
|
C | G | 86 | a0001c0001t0003g0324a0001c0002t0002g0001a0001c0002t0002g0116others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.153+992G>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986538 | ||||||
| chr6:138986628
|
A | G | 8 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+902T>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986628 | ||||||
| chr6:138986763
|
CCT | C | 28 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018others(25): Show | 28 | HG01069.hp1 HG01192.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+765_153+766del others(2): Show |
REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986763 | ||||||
| chr6:138986787
|
T | TA | 4 | a0001c0001t0001g0004a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+742dupT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986787 | ||||||
| chr6:138986787
|
TA | T | 75 | a0001c0001t0003g0324a0001c0002t0003g0318a0001c0002t0003g0319others(72): Show | 75 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.153+742delT | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986787 | ||||||
| chr6:138986986
|
T | A | 1 | a0001c0001t0002g0107 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.153+544A>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138986986 | ||||||
| chr6:138987012
|
G | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 318 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.153+518C>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138987012 | ||||||
| chr6:138987024
|
T | G | 1 | a0007c0009t0001g0303 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.153+506A>C | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138987024 | ||||||
| chr6:138987106
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.153+424C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138987106 | ||||||
| chr6:138987121
|
C | T | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 318 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.153+409G>A | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138987121 | ||||||
| chr6:138987179
|
G | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 215 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.153+351C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138987179 | ||||||
| chr6:138987256
|
C | A | 73 | a0001c0001t0003g0324a0001c0002t0003g0318a0001c0002t0003g0319others(70): Show | 73 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.153+274G>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138987256 | ||||||
| chr6:138987257
|
A | C | 3 | a0002c0003t0004g0016a0002c0003t0004g0017a0002c0003t0004g0018 | 3 | HG02258.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.153+273T>G | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138987257 | ||||||
| chr6:138987265
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.153+265C>T | REPS1 | ENSG00000135597.19 | transcript | ENST00000450536.7 | protein_coding | 1/19 | chr6 | 138987265 |